<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2023</YEAR>
<VOL>27</VOL>
<NO>1</NO>
<MOSALSAL>0</MOSALSAL>
<PAGE_NO>99</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>The effect of erythropoietin on cardiac and neurotoxicity induced by carbon monoxidepoisoning</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Carbon monoxide (CO) intoxication is one of the most important poisonings related to high morbidity and mortality rate. The main treatment of CO poisoning is oxygen therapy using normobaric (NBO) or hyperbaric oxygen (HBO). However, more pharmaceutical agents are needed to improve CO poisoning treatment, especially in severe cases. Recently, erythropoietin (EPO) has been examined in several studies, showing a significant reduction in cardiac and neural sequels of CO poisoning.In this article, the effect of EPO on cardio and neurotoxicity of CO poisoning were reviewed. For this purpose, EPO effect on CO poisoning was searched in papers published until 2020 using Pubmed, Scopus, and google scholar. Only English papers on three main databases have been reviewed. The review of several animal and clinical studies have been shown that EPO administration after CO poisoning could improve neurological function and reduce CO-neurotoxicity significantly. Although there is good evidence of EPO effects on CO-induced-neurological sequelae, further clinical studies are needed to establish its benefit on CO intoxication.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>1</FPAGE>
			<TPAGE>8</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/26
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/8/5
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/5
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/10/15
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Seyed Adel</Name>
				<MidName></MidName>
				<Family>Moallem</Family>
				<NameE>Seyed Adel</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Moallem</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mitra</Name>
				<MidName></MidName>
				<Family>Asgharian Rezaee</Family>
				<NameE>Mitra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Asgharian Rezaee</FamilyE>
				<Organizations>
				<Organization>Department of Toxicology and Pharmacology, Faculty of Pharmacy, Kerman University of Medical Sciences, Kerman, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Rezaeem@kmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Amirhooshang</Name>
				<MidName></MidName>
				<Family>Mohammadpour</Family>
				<NameE>Amirhooshang</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mohammadpour</FamilyE>
				<Organizations>
				<Organization>Department of clinical pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohsen</Name>
				<MidName></MidName>
				<Family>Imenshahidi</Family>
				<NameE>Mohsen</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Imenshahidi</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Carbon monoxide poisoning</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Erythropoietin</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cardiotoxicity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Neurotoxicity</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Alireza Nekoui G B. Erythropoietin and Non-Hematopoietic Effects: Review Article. AM J MED SCI 2017; 353: 76-81.##Asgharian Rezaee M, Moallem S A, Imenshahidi M, Farzadnia M, Mohammadpour A H. Effects of erythropoietin on electrocardiogram changes in carbon monoxide poisoning: an experimental study in rats. Iran J Pharm Res 2012; 11: 1191-9.##Aydin A G K, Akhisaroglu M, Yorukogluc K, Gokmen N, Gonullu E. Erythropoietin exerts neuroprotective effect in neonatal rat model of hypoxic-ischemic brain injury. Brain Dev 2003; 25: 494-498.##Burger D, Xenocostas A, Feng Q P. Molecular basis of cardioprotection by erythropoietin. Curr Mol Pharmacol 2009; 2: 56-69.##Chiew A L, Buckley N A. Carbon monoxide poisoning in the 21st century. Crit. Care 2014; 18: 221.##Choi I S. Parkinsonism after carbon monoxide poisoning. Eur Neurol 2002; 48: 30-3.##Dame C J S, Christensen RD. The biology of erythropoietin in the central nervous system and its neurotrophic and neuroprotective potential. Biol Neonate 2001; 79: 228-235.##Danold S Silerberg D w, Miriam Blum, Adian Laina, David Sheps, Gad Keren, Doron Schwartz. Erythropoiein in heart failure Semin nephrol 2005; 25: 3997-403.##Dubrey S W, Chehab O, Ghonim S. Carbon monoxide poisoning: an ancient and frequent cause of accidental death. Br J Hosp Med (Lond) 2015; 76: 159-62.##Eichhorn L, Thudium M, Jüttner B. The Diagnosis and Treatment of Carbon Monoxide Poisoning. Dtsch Arztebl Int 2018; 115: 863-870.##EJ L. carbon monoxide poisoning. In: Shannon MW BS, Burns M, editor. Haddad and Winchester's clinical management of poisoning and drug overdose. Philadelphia: Saunders/Elsevier, 2007: 1297-1307.##Florian Simon N F, Wiebke Ibing, Hubert Schelzig, Artis Knapsis. Neurotherapeutic potential of erythropoietin after ischemic injury of the central nervous system. Neural Regen Res 2019; 14: 1309-1312.##François Roubille F P, Stéphanie Barrère-Lemaire, Florence Leclercq, Christophe Piot, Ekaterini A. Kritikou, Eric Rhéaume, David Busseuil, Jean-Claude Tardif. What is the Role of Erythropoietin in Acute Myocardial Infarct? Bridging the Gap Between Experimental Models and Clinical Trials. Cardiovasc Drugs Ther 2013; 27: 315-331.##Gandini C, Castoldi A F, Candura S M, Locatelli C, Butera R, Priori S, et al. Carbon monoxide cardiotoxicity. J Toxicol Clin Toxicol 2001; 39: 35-44.##Ghezzi P, Brines M. Erythropoietin as an antiapoptotic, tissue-protective cytokine. Cell Death Differ 2004; 11: S37-S44.##Guzman J A. Carbon monoxide poisoning. Crit Care Clin 2012; 28: 537-48.##Hannelore Ehrenreich, Martin Hasselblatt, Christoph Dembowski, Lukas Cepek, Piotr Lewczuk, Michael Stiefel, et al. Erythropoietin Therapy for Acute Stroke Is Both Safe and Beneficial. Mol. Med 2002; 8: 495-505.##Henry C R, Satran D, Lindgren B, Adkinson C, Nicholson C I, Henry T D. Myocardial injury and long-term mortality following moderate to severe carbon monoxide poisoning. Jama 2006; 295: 398-402.##Jelkmann W. Molecular biology of erythropoietin. Intern. Med 2004; 43: 649-659.##Joyeux-Faure M, Godin-Ribuot D, Ribuot C. Erythropoietin and myocardial protection: what's new. Fundam Clin Pharmacol 2005; 19: 439-46.##Kao H-W, Cho N-Y, Hsueh C-J, Chou M-C, Chung H-W, Liou M, et al. Delayed Parkinsonism after CO Intoxication: Evaluation of the Substantia Nigra with Inversion-Recovery MR Imaging. Radiology 2012; 265: 215-221.##Katavetin P, Tungsanga K, Eiam-Ong S, Nangaku M. Antioxidative effects of erythropoietin. Kidney Int 2007; 72: S10-S15.##Kaveh Abri Aghdam M S S, Khalil Ghasemi Falavarjani. Erythropoietin in ophthalmology: A literature review. J. Curr. Ophthalmol. 2016; 28: 5-11.##Kinoshita H, Türkan H, Vucinic S, Naqvi S, Bedair R, Rezaee R, et al. Carbon monoxide poisoning. Toxicol. Rep 2020; 7: 169-173.##Lai C-Y, Chou M-C, Lin C-L, Kao C-H. Increased risk of Parkinson disease in patients with carbon monoxide intoxication: a population-based cohort study. Medicine 2015; 94: e869-e869.##Lawrence T. The nuclear factor NF-kappaB pathway in inflammation. Cold Spring Harb Perspect Biol 2009; 1: 1-10.##Li Y, Hu X, Lu Z. Erythropoietin in the treatment of encephalopathy associated with carbon monoxide poisoning. Prog Neuropsychopharmacol Biol Psychiatry 2009; 33: 735-8.##Lippi G, Rastelli G, Meschi T, Borghi L, Cervellin G. Pathophysiology, clinics, diagnosis and treatment of heart involvement in carbon monoxide poisoning. Clin Biochem 2012; 45: 1278-85.##Mastromarino V, Musumeci M B, Conti E, Tocci G, Volpe M. Erythropoietin in cardiac disease: effective or harmful? J Cardiovasc Med (Hagerstown) 2013; 14: 870-8.##Moallem S A, Mohamadpour A H, Abnous K, Sankian M, Sadeghnia H R, Tsatsakis A, et al. Erythropoietin in the treatment of carbon monoxide neurotoxicity in rat. Food Chem Toxicol 2015; 86: 56-64.##Nguyen A Q, Cherry B H, Scott G F, Ryou M G, Mallet R T. Erythropoietin: powerful protection of ischemic and post-ischemic brain. Exp Biol Med (Maywood) 2014; 239: 1461-75.##Oh S, Choi S-C. Acute carbon monoxide poisoning and delayed neurological sequelae: a potential neuroprotection bundle therapy. Neural Regen Res 2015; 10: 36-38.##Pang L, Bian M, Zang X X, Wu Y, Xu D H, Dong N, et al. Neuroprotective effects of erythropoietin in patients with carbon monoxide poisoning. J Biochem Mol Toxicol 2013; 27: 266-71.##Pang L, Zhang N, Dong N, Wang D W, Xu D H, Zhang P, et al. Erythropoietin Protects Rat Brain Injury from Carbon Monoxide Poisoning by Inhibiting Toll-Like Receptor 4/NF-kappa B-Dependent Inflammatory Responses. Inflammation 2016; 39: 561-8.##Paschos N, Lykissas M G, Beris A E. The role of erythropoietin as an inhibitor of tissue ischemia. Int J Biol Sci 2008; 4: 161-8.##Peng B, Kong G, Yang C, Ming Y. Erythropoietin and its derivatives: from tissue protection to immune regulation. Cell Death Dis 2020; 11: 79.##Prockop L D, Chichkova R I. Carbon monoxide intoxication: an updated review. J Neurol Sci 2007; 262: 122-30.##Rezaee M A, Moallem S A, Mohammadpour A H, Mahmoudi M, Sankian M, Farzadnia M, et al. Histopathological study of erythropoietin protective effect on carbon monoxide-induced cardiotoxicity in rat. Iran J Basic Med Sci 2017; 20: 1189-1193.##Rezaee M A, Mohammadpour A H, Imenshahidi M, Mahmoudi M, Sankian M, Tsarouhas K, et al. Protective effect of erythropoietin on myocardial apoptosis in rats exposed to carbon monoxide. Life Sci 2016; 148: 118-24.##Rose J J, Wang L, Xu Q, McTiernan C F, Shiva S, Tejero J, et al. Carbon Monoxide Poisoning: Pathogenesis, Management, and Future Directions of Therapy. Am J Respir Crit Care Med 2017; 195: 596-606.##S. Shahsavand S M, A. Mohhamadpour. Evaluation of erythropoietin effect on cellular neurotoxicity after carbon monoxide poisoning in rat. Res Pharm Sci 2012; 7: 5.##Santhanam A V R, d'Uscio L V, Katusic Z S. Cardiovascular effects of erythropoietin an update. Adv. Pharmacol 2010; 60: 257-285.##Sasaki R. Pleiotropic functions of erythropoietin. Intern Med 2003; 42: 142-9.##Seyed Mohammad Hosseininejad H A, Iraj Goli Khatir, Seyed Khosro Ghasempouri, Ali Jabbari, Mahmoud Khandashpour. Carbon monoxide poisoning in Iran during 1999-2016: A systematic review and metaanalysis. J Forensic Leg Med 2018; 53: 87-96.##Shahsavand S, Mohammadpour A H, Rezaee R, Behravan E, Sakhtianchi R, Moallem S A. Effect of Erythropoietin on Serum Brain-derived Biomarkers after Carbon Monoxide Poisoning in Rats. Iran J Basic Med Sci 2012; 15: 752-8.##Shi Y, Rafiee P, Su J, Pritchard K A, Jr., Tweddell J S, Baker J E. Acute cardioprotective effects of erythropoietin in infant rabbits are mediated by activation of protein kinases and potassium channels. Basic Res Cardiol 2004; 99: 173-82.##Weaver L K. Clinical practice. Carbon monoxide poisoning. N Engl J Med 2009; 360: 1217-25.##Wu P E, Juurlink D N. Carbon monoxide poisoning. CMAJ 2014; 186: 611-611.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Umbilical cord as a source of mesenchymal stem cells improves melasma in parturients: a clinicalrandomized trial</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Melasma is a common skin problem in pregnant women that appears to be related to physiological changes. Mesenchymal stem cells (MSCs) have been used to treat skin disorders because of their direct cell-to-cell contact or release of several biomolecules. The umbilical cord, which is available at birth, is a rich source of MSCs. This study was undertaken to evaluate the effect of the umbilical cord as a natural face mask for treating women&#8217;s melasma after parturition.
Methods: This randomized clinical trial was carried out on parturients suffering from melasma. Fifty pregnant women were randomly categorized into two groups of control and treated with the umbilical cord. A section of the umbilical cord (10-20 cm) was cut immediately after parturition and used as a face mask on the face of each mother in the hyperpigmentation areas for one hour. Melasma Area Severity Index (MASI) was used to measure hyperpigmentation and calculated for each participant before and four weeks after intervention.
Results: A significant decrease in MASI was observed in the women treated with the umbilical cord (p&#60;0.05).
Conclusion: Our findings suggested that a fresh umbilical cord, as a natural face mask containing MSCs, can improve the melasma in the parturients.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>9</FPAGE>
			<TPAGE>15</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/17
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/3/27
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/8
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/3/18
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Adelipour</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Adelipour</FamilyE>
				<Organizations>
				<Organization>Department of Biochemistry, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hanan</Name>
				<MidName></MidName>
				<Family>Sorkheh</Family>
				<NameE>Hanan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sorkheh</FamilyE>
				<Organizations>
				<Organization>Abadan University of Medical Science, Abadan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Zohreh</Name>
				<MidName></MidName>
				<Family>Kiani</Family>
				<NameE>Zohreh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kiani</FamilyE>
				<Organizations>
				<Organization>Faculty of Nursing and Midwifery, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Houria</Name>
				<MidName></MidName>
				<Family>Bahrami</Family>
				<NameE>Houria</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bahrami</FamilyE>
				<Organizations>
				<Organization>Abadan University of Medical Science, Abadan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Neda</Name>
				<MidName></MidName>
				<Family>Berageah</Family>
				<NameE>Neda</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Berageah</FamilyE>
				<Organizations>
				<Organization>Faculty of Nursing and Midwifery, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Anayat</Name>
				<MidName></MidName>
				<Family>Salimi</Family>
				<NameE>Anayat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Salimi</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Department of Pharmaceutics, Faculty of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mahshid</Name>
				<MidName></MidName>
				<Family>Naghashpour</Family>
				<NameE>Mahshid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Naghashpour</FamilyE>
				<Organizations>
				<Organization>Department of Nutrition, School of Medicine, Abadan University of Medical Sciences, Abadan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Atefeh</Name>
				<MidName></MidName>
				<Family>Zahedi</Family>
				<NameE>Atefeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Zahedi</FamilyE>
				<Organizations>
				<Organization>Asadabad School of medical sciences, Asadabad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sahar</Name>
				<MidName></MidName>
				<Family>Golabi</Family>
				<NameE>Sahar</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Golabi</FamilyE>
				<Organizations>
				<Organization>Department of Medical Physiology, School of Medicine, Abadan University of Medical Sciences, Abadan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>s.golabi@abadanums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Umbilical cord</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Mesenchymal stem cells</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pregnancy</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Bajetto A, Pattarozzi A, Corsaro A, Barbieri F, Daga A, Bosio A, et al. Different effects of human umbilical cord mesenchymal stem cells on glioblastoma stem cells by direct cell interaction or via released soluble factors. Front Cell Neurosci 2017; 11: 312.##Barankin B, Silver SG, Carruthers A. The skin in pregnancy. J Cutan Med Surg 2002; 6: 236-40.##Chen H, Niu J-W, Ning H-M, Pan X, Li X-B, Li Y, et al. Treatment of psoriasis with mesenchymal stem cells. Am J Med 2016; 129: 13-14.##Ezquer FE, Ezquer ME, Vicencio JM, Calligaris SD. Two complementary strategies to improve cell engraftment in mesenchymal stem cell-based therapy: Increasing transplanted cell resistance and increasing tissue receptivity. Cell Adh Migr 2017; 11: 110-9.##Geraghty LN, Pomeranz MK. Physiologic changes and dermatoses of pregnancy. Int J Dermatol 2011; 50: 771-82.##Grimes P, Ijaz S, Nashawati R, Kwak D. New oral and topical approaches for the treatment of melasma. Int J Womens Dermatol 2019; 5: 30-6.##Gupta AK, Gover MD, Nouri K, Taylor S. The treatment of melasma: a review of clinical trials. J Am Acad Dermatol 2006; 55: 1048-65.##Hughes EC, Saleh D. Telogen effluvium. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing 2017.##Lakhdar H, Zouhair K, Khadir K, Essari A, Richard A, Seité S, et al. Evaluation of the effectiveness of a broad-spectrum sunscreen in the prevention of chloasma in pregnant women. J Eur Acad Dermatol Venereol 2007; 21: 738-42.##Lee JH, Park JG, Lim SH, Kim JY, Ahn KY, KIM MY, et al. Localized intradermal microinjection of tranexamic acid for treatment of melasma in Asian patients: a preliminary clinical trial. Dermatol Surg 2006; 32: 626-31.##McKesey J, Tovar-Garza A, Pandya AG. Melasma treatment: An Evidence-Based Review. Am J Clin Dermatol 2019: 1-53.##Ortonne J-P, Bissett DL. Latest insights into skin hyperpigmentation. J Investig Dermatol Symp Proc 2008;13(1):10-4.##Shin T-H, Kim H-S, Choi SW, Kang K-S. Mesenchymal stem cell therapy for inflammatory skin diseases: Clinical potential and mode of action. Int J Mol Sci 2017; 18: 244.##Shojaei F, Rahmati S, Banitalebi Dehkordi M. A review on different methods to increase the efficiency of mesenchymal stem cell-based wound therapy. Wound Repair Regen 2019; 27: 661-71.##Sivakumaran N, Rathnayaka IR, Shabbir R, Wimalsinghe SS, Jayakody J, Chandrasekaran M. Umbilical cord blood banking and its therapeutic uses. Int j sci res innov technol 2018; 5: 160.##Teresa Conconi M, Di Liddo R, Tommasini M, Calore C, Paolo Parnigotto P. Phenotype and differentiation potential of stromal populations obtained from various zones of human umbilical cord: an overview. J Tissue Eng Regen Med 2011; 4.##Urasaki MBM. Skin physiological alterations perceived by pregnant women attended at public health services. Acta Paulista de Enfermagem 2010; 23: 519-25.##Wagner W, Wein F, Seckinger A, Frankhauser M, Wirkner U, Krause U, et al. Comparative characteristics of mesenchymal stem cells from human bone marrow, adipose tissue, and umbilical cord blood. Exp Hematol 2005; 33: 1402-16.##Wang HS, Hung SC, Peng ST, Huang CC, Wei HM, Guo YJ, et al. Mesenchymal stem cells in the Wharton’s jelly of the human umbilical cord. Stem Cells 2004; 22: 1330-7.##Wu Y, Huang S, Enhe J, Ma K, Yang S, Sun T, et al. Bone marrow-derived mesenchymal stem cell attenuates skin fibrosis development in mice. Int Wound J 2014; 11: 701-10.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Respiratory Exchange Ratio in Obese and Non- obese Sedentary Indian Young Adults in Moderate-and Vigorous-intensity Exercise</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Respiratory exchange ratio (RER) is the ratio between produced CO2 and used O2 for body metabolism. It indicates the type of fuel that is metabolized in the body. This study aimed to measure and compare the RER in non-obese and obese sedentary young adults in rest, moderate-intensity, and vigorous-intensity exercise.
Methods: This cross-sectional study was conducted with 23 non-obese and 24 obese sedentary young adults. Resting RER was measured with 12-h fasting after 15-min rest with an automated gas analyzer. Then, RER was measured during steady moderate-intensity and vigorous-intensity exercise on a cycle ergometer. RER was compared between males and females, non-obese and obese in resting, moderate-intensity, and vigorous-intensity exercise by t-test.
Results: The Mean age of the non-obese and obese groups was 19.35&#177;1.11 and 19.79&#177;0.78 years, respectively. Males showed higher RER (in resting and moderate-intensity exercise) than females. In comparison to non-obese group, the obese group showed higher RER in resting (0.802&#177;0.018 versus 0.821&#177;0.022, P=0.001), moderate-intensity exercise (0.812&#177;0.013 versus 0.83&#177;0.02, P&#60;0.001), and vigorous-intensity exercise (0.853&#177;0.43 versus 0.914&#177;0.032, P&#60;0.001). Concerning resting value, RER significantly increased during moderate- and vigorous-intensity exercise in both the non-obese and obese groups.
Conclusion: Obese young adults use relatively more carbohydrates as fuel than non-obese in both resting conditions and during exercise. When the intensity of exercise increased, both obese and non-obese showed higher RER which indicates that sedentary young adults use relatively more carbohydrates as fuel in the higher grade of exercise.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>16</FPAGE>
			<TPAGE>27</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/27
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/6/5
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/4
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/9/13
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Debasish</Name>
				<MidName></MidName>
				<Family>Das</Family>
				<NameE>Debasish</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Das</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Fakir Mohan Medical College and Hospital, Balasore, Odisha, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Amit Kumar</Name>
				<MidName></MidName>
				<Family>Das</Family>
				<NameE>Amit Kumar</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Das</FamilyE>
				<Organizations>
				<Organization>Department of Medicine, Nil Ratan Sircar Medical College, Kolkata, West Bengal, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shaikat</Name>
				<MidName></MidName>
				<Family>Mondal</Family>
				<NameE>Shaikat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mondal</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Raiganj Government Medical College and Hospital, Raiganj, West Bengal, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Himel</Name>
				<MidName></MidName>
				<Family>Mondal</Family>
				<NameE>Himel</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mondal</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, All India Institute of Medical Sciences, Deoghar, Jharkhand, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>physiology@smcbangla.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Rabindranath</Name>
				<MidName></MidName>
				<Family>Majumder</Family>
				<NameE>Rabindranath</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Majumder</FamilyE>
				<Organizations>
				<Organization>Centre of Healthcare Science and Technology, Indian Institute of Engineering Science and Technology, Shibpur, West Bengal, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Adipose tissue</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Carbohydrates</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Diet</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Obesity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Respiratory quotient</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Young adult.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Adams R. Revised Physical Activity Readiness Questionnaire. Can Fam Physician 1999;45:992‐1005.##Arad AD, Basile AJ, Albu J, DiMenna FJ. No Influence of Overweight/Obesity on Exercise Lipid Oxidation: A Systematic Review. Int J Mol Sci 2020;21:1614.##Balcı SS. Comparison of substrate oxidation during walking and running in normal-weight and overweight/obese men. Obes Facts 2012;5:327‐38.##Beatty J, Melanson K. Examining changes in respiratory exchange ratio within an 8-week weight loss intervention. J Hum Nutr Diet 2019;32:737‐44.##Cavuoto LA, Maikala RV. Obesity and the Role of Short Duration Submaximal Work on Cardiovascular and Cerebral Hemodynamics. PLoS One 2016;11:e0153826.##Chatzinikolaou A, Fatouros I, Petridou A, Jamurtas A, Avloniti A, Douroudos I, et al. Adipose tissue lipolysis is upregulated in lean and obese men during acute resistance exercise. Diabetes Care 2008;31:1397‐9.##Coggan AR, Raguso CA, Gastaldelli A, Sidossis LS, Yeckel CW. Fat metabolism during high-intensity exercise in endurance-trained and untrained men. Metabolism 2000;49:122-8.##Geerling BJ, Alles MS, Murgatroyd PR, Goldberg GR, Harding M, Prentice AM. Fatness in relation to substrate oxidation during exercise. Int J Obes Relat Metab Disord 1994;18:453‐9.##Ghasemi A, Zahediasl S. Normality tests for statistical analysis: a guide for non-statisticians. Int J Endocrinol Metab 2012;10:486-9.##Goedecke JH, St Clair Gibson A, Grobler L, Collins M, Noakes TD, Lambert EV. Determinants of the variability in respiratory exchange ratio at rest and during exercise in trained athletes. Am J Physiol Endocrinol Metab 2000;279:E1325-34.##Goodpaster BH, Wolfe RR, Kelley DE. Effects of obesity on substrate utilization during exercise. Obes Res 2002;10:575‐84.##Gupta RD, Ramachandran R, Venkatesan P, Anoop S, Joseph M, Thomas N. Indirect calorimetry: From bench to bedside. Indian J Endocr Metab 2017;21:594-9.##Haugen HA, Chan LN, Li F. Indirect calorimetry: a practical guide for clinicians. Nutr Clin Pract 2007;22:377‐88.##Hirsch KR, Smith-Ryan AE, Blue MN, Mock MG, Trexler ET, Ondrak KS. Metabolic characterization of overweight and obese adults. Phys Sportsmed 2016;44:362‐72.##Houmard JA. Intramuscular lipid oxidation and obesity. Am J Physiol Regul Integr Comp Physiol 2008;294:R1111‐6.##Kyle UG, Gremion G, Genton L, Slosman DO, Golay A, Pichard C. Physical activity and fat-free and fat mass by bioelectrical impedance in 3853 adults. Med Sci Sports Exerc 2001;33:576‐84.##Leicht AS, Sinclair WH, Spinks WL. Effect of exercise mode on heart rate variability during steady state exercise. Eur J Appl Physiol 2008;102:195-204.##Magnon V, Dutheil F, Auxiette C. Sedentariness: A Need for a Definition. Front Public Health 2018;6:372.##Mahajan K, Batra A. Obesity in adult asian indians- the ideal BMI cut-off. Indian Heart J 2018;70:195.##Misra A, Chowbey P, Makkar BM, Vikram NK, Wasir JS, Chadha D, et al. Consensus statement for diagnosis of obesity, abdominal obesity and the metabolic syndrome for Asian Indians and recommendations for physical activity, medical and surgical management. J Assoc Physicians India 2009;57:163‐70.##Mittendorfer B, Fields DA, Klein S. Excess body fat in men decreases plasma fatty acid availability and oxidation during endurance exercise. Am J Physiol Endocrinol Metab 2004;286:E354‐62.##Mittendorfer B, Horowitz JF, Klein S. Effect of gender on lipid kinetics during endurance exercise of moderate intensity in untrained subjects. Am J Physiol Endocrinol Metab 2002;283:E58‐65.##Mondal H, Mishra SP. Effect of BMI, Body Fat Percentage and Fat Free Mass on Maximal Oxygen Consumption in Healthy Young Adults. J Clin Diagn Res 2017;11:CC17-20.##Mondal H, Mondal S, Baidya C. Competency in home body fat monitoring by portable devices based on bioelectrical impedance analysis: A pilot study. J Educ Health Promot 2019;8:223.##Mul JD, Stanford KI, Hirshman MF, Goodyear LJ. Exercise and Regulation of Carbohydrate Metabolism. Prog Mol Biol Transl Sci 2015;135:17‐37.##Pendergast DR, Leddy JJ, Venkatraman JT. A perspective on fat intake in athletes. J Am Coll Nutr 2000;19:345-50.##Pérez-Martin A, Dumortier M, Raynaud E, Brun JF, Fédou C, Bringer J, et al. Balance of substrate oxidation during submaximal exercise in lean and obese people. Diabetes Metab 2001;27:466‐74.##Ramos-Jiménez A, Hernández-Torres RP, Torres-Durán PV, Romero-Gonzalez J, Mascher D, Posadas-Romero C, et al. The Respiratory Exchange Ratio is Associated with Fitness Indicators Both in Trained and Untrained Men: A Possible Application for People with Reduced Exercise Tolerance. Clin Med Circ Respirat Pulm Med 2008;2:1‐9.##Rimbert V, Boirie Y, Bedu M, Hocquette JF, Ritz P, Morio B. Muscle fat oxidative capacity is not impaired by age but by physical inactivity: association with insulin sensitivity. FASEB J 2004;18:737‐9.##Roy S, McCrory J. Validation of Maximal Heart Rate Prediction Equations Based on Sex and Physical Activity Status. Int J Exerc Sci 2015;8:318-30.##Schrauwen P, van Aggel-Leijssen DP, Hul G, Wagenmakers AJM, Vidal H, Saris WHM, et al. The effect of a 3-month low-intensity endurance training program on fat oxidation and acetyl-CoA carboxylase-2 expression. Diabetes 2002;51:2220‐6.##Smorawiński J, Nazar K, Kaciuba-Uscilko H, Kamińska E, Cybulski G, Kodrzycka A, et al. Effects of 3-day bed rest on physiological responses to graded exercise in athletes and sedentary men. J Appl Physiol 2001;91:249-57.##Shen T, Wen X. Heart-rate-based prediction of velocity at lactate threshold in ordinary adults. J Exerc Sci Fit 2019;17:108-112.##Toth MJ, Gardner AW, Arciero PJ, Calles-Escandon J, Poehlman ET. Gender differences in fat oxidation and sympathetic nervous system activity at rest and during submaximal exercise in older individuals. Clin Sci (Lond) 1998;95:59‐66.##Verma M, Rajput M, Kishore K, Kathirvel S. Asian BMI criteria are better than WHO criteria in predicting Hypertension: A cross-sectional study from rural India. J Family Med Prim Care 2019;8:2095-2100.##Vilchis-Gil J, Galván-Portillo M, Klünder-Klünder M, Cruz M, Flores-Huerta S. Food habits, physical activities and sedentary lifestyles of eutrophic and obese school children: a case-control study. BMC Public Health 2015;15:124.##Villareal DT, Apovian CM, Kushner RF, Klein S; American Society for Nutrition; NAASO, The Obesity Society. Obesity in older adults: technical review and position statement of the American Society for Nutrition and NAASO, The Obesity Society. Am J Clin Nutr 2005;82:923‐34.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>A comparative study of the efficacy of “Think-Pair- Share” method over tutorials in Pharmacology forundergraduates</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: &#8220;Think&#8211;Pair&#8211;Share&#8221; (TPS) is an active cooperative teaching-learning method that encourages as well as allows for individual thinking, collaboration, and presentation. It offers the benefits of small group learning and the development of higher-order thinking skills. It provides immediate feedback to students on their understanding and teachers on the extent of pupil understanding. Thus it helps in modifying both teaching and learning. Hence the current study aimed at comparing the efficacy of TPS with tutorials and assessing the perception of students towards TPS.
Methods: 42 students who met the eligibility criteria and consented to participate in the study were included after obtaining Institutional ethics committee clearance and written informed consent. There were 2 test groups. TPS was employed to teach Group 1 while Group 2 was taught by Tutorials simultaneously for 6 sessions. A pre-test and post-test were conducted for each session. A final Multiple choice question test was conducted at the end of the study. The perception of the participants towards TPS was also obtained.
Results: Our study did not show a significant difference between the post-test, change in mean post-test over pre-test scores, and final test scores. The participants had a good perception regarding TPS and agreed that it was engaging and improved communication with the teacher. They felt that it also should be used in the future.
Conclusion: Although TPS failed to exhibit an improved efficacy, it can be used in the future because it promotes active learner participation, individual thinking, and communication skills as well as provides immediate feedback.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>28</FPAGE>
			<TPAGE>33</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/13
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/10/23
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/21
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/2/31
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Megaravalli R</Name>
				<MidName></MidName>
				<Family>Manasa</Family>
				<NameE>Megaravalli R</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Manasa</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology, Karwar Institute of medical sciences, Rajiv Gandhi University of Health Sciences, Karwar, Karnataka, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email>manasamr.acme@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Chaitanya</Name>
				<MidName></MidName>
				<Family>Karant</Family>
				<NameE>Chaitanya</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Karant</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology, Karwar Institute of medical sciences, Rajiv Gandhi University of Health Sciences, Karwar, Karnataka, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shilpa</Name>
				<MidName></MidName>
				<Family>Bhimalli</Family>
				<NameE>Shilpa</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bhimalli</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, KAHER Jawaharlal Nehru Medical College, Belagavi, Karnataka, India</Organization>
				</Organizations>
				<Countries>
				<Country>India</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Think-Pair-Share</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pharmacology</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Undergraduates.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Ariana S. Finding the effects of think-pair-share on student confidence and participation. Honors Projects 2013; 28.##Black P, William D. Assessment and classroom learning. Assess Educ.: Princ Policy Pract 1998; 51: 7-74. https://doi.org/10.1080/0969595980050102.##Bonwell CC, Eison JA. Active learning: Creating excitement in the classroom. Washington, DC: School of Education and Human Development. George Washington University, 1991.##Freeman S, Eddy SL, McDonough M, Smith MK, Okoroafor N, Jordt H et al. Active learning increases student performance in science, engineering, and mathematics. Proc Natl Acad Sci 2014; 111(23): 8410-15. https://doi.org/10.1073/pnas.1319030111##Gok T. A comparison of students’ performance, skill and confidence with peer instruction and formal education. J Balt Sci Educ 2013; 12(6), 747-58. https://doi.org/10.33225/jbse/13.12.747##Giancarlo CA, Facione PA. A look across four years at the disposition toward critical thinking among undergraduate students. J Gen Educ 2007; 5(91):29-55. https://doi.org/10.1353/jge.2001.0004 ##Hamdan RKA. The Effect of (Think - Pair - Share) strategy on the achievement of third grade student in sciences in the educational district of irbid. J educ pract 2017; 8(9): 88-95.##Kaddoura M. Think Pair Share: A teaching learning strategy to enhance students’ critical thinking. Educ Res Quart 2013; 36(4):3-24.##Karge BD, Phillips KM, Jessee T, McCabe M. Effective strategies for engaging adult learners. J Coll Sci Teach 2011; 8:53-6. https://doi.org/10.19030/tlc.v8i12.6621##Kumar R, Upadhyay AK. Effectiveness of think-pair-share technique over conventional technique in promoting science education at upper primary standard. Int J Educ Res 2016, 2(11): 89-90.##Ledlow S. Using think-pair-share in the college classroom. center for learning and teaching excellence, Arizona State University, 2001.##Lujan H, DiCarlo SE. Too much teaching, not enough learning: what is the solution? Adv Physiol Educ 2005; 30(1):17-22. https://doi.org/10.1152/advan.00061.2005.##MacDougall C. A novel teaching tool combined with active-learning to teach antimicrobial spectrum activity. Am J Pharm Educ 2017; 81: 25. https://doi.org/10.5688/ajpe81225##McDermott LC. Millikan Lecture 1990: What we teach and what is learned-Closing the gap. Am J Phys, 1991; 59(4), 301-15. https://doi.org/10.1119/1.16539. ##Medical council of India, 2017, http://www.mciindia.org/tools/announcement/ MCI_booklet.pdf (accessed 21.5.17).##Nagel P. Moving beyond lecture: Cooperative learning and the secondary social studies classroom. Education Chula Vista, 2008; 128(3):363-8.##Nwaubani OO, Ogbueghu SN, Adeniyi KD, Eze DM. Effects of think-pair-share (TPS) and student-teams-achievement divisions (STAD) instructional strategies on senior secondary school students’ achievement in economics. Austr J Basic Appl Sci 2016; 10(13):1-9.##Sapsuha S, Bugis R. Think pair share technique to improve students’ reading comprehension. ICE-Ed conference. ICE-Ed conference. ELT Practices in Asia: Challenges and Opportunities, 2013.##Sumekto DR. Investigating the influence of think-pair-share approach toward students’ reading achievement. Lingua Cultura 2018; 12(2):195-202. https://doi.org/10.21512/lc.v12i2.4011 ##Zaini RG. Student’s feedback regarding the think pair share strategy in haematology class. Educ Res Rev 2020; 8(1): 16-20.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Sex influences on sensory responses followingspinothalamic tract injury in rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: There is some evidence of significant differences in the recovery after spinal cord injury (SCI) between males and females. In this study, we investigated the sensory function and involvement of astrocytes in the sex differences of central pain syndrome in the unilateral spinothalamic tract (STT) injury model in rats.
Methods: Rats were divided into two groups: SCI and Sham groups received a unilateral electrolytic lesion on STT at T8-T9 and a control sham surgery respectively. After recovery from surgery, the sensory function was monitored for 28 days using tail flick and von Frey filament tests. The glial fibrillary acidic protein (GFAP) level was also measured by Western blot at the same time points.
Results: Mechanical hypersensitivity was increased from days 3 to 28 post-injury in male rats (P&#60;0.001), but no significant change was observed in females. In the tail flick model, male rats had significantly elevated thermal withdrawal latency on day3 after STT lesion, while females showed a reduction in latency (P&#60;0.001). Sex differences in GFAP level were observed during 4 weeks of study after injury. Results in the first week showed that GFAP level decreased in females, but the marked elevation was observed from days 7 to 28 in males (P&#60;0.05).
Conclusion: This study revealed the sex differences in sensory dysfunction and the related astrocyte reactivity after SCI. It suggests a need for more studies using both sexes to fully explore the influence of sex on the recovery of sensory impairments post-SCI.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>34</FPAGE>
			<TPAGE>41</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/17
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/5/26
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/30
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/3/9
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Abbaszadeh</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Abbaszadeh</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mina</Name>
				<MidName></MidName>
				<Family>Afhami</Family>
				<NameE>Mina</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Afhami</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Elham</Name>
				<MidName></MidName>
				<Family>Saghaei</Family>
				<NameE>Elham</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Saghaei</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Kobra</Name>
				<MidName></MidName>
				<Family>Naseri</Family>
				<NameE>Kobra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Naseri</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Majid</Name>
				<MidName></MidName>
				<Family>Hassanpour-ezatti</Family>
				<NameE>Majid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hassanpour-ezatti</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Faculty of Basic Science, Shahed University, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Masoumeh</Name>
				<MidName></MidName>
				<Family>Jorjani</Family>
				<NameE>Masoumeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Jorjani</FamilyE>
				<Organizations>
				<Organization>Neurobiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>msjorjani@sbmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Sex differences</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Spinal cord injury</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Sensory hypersensitivity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Astrocyte reactivity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Rat.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Acaz-Fonseca E, Sanchez-Gonzalez R, Azcoitia I, Arevalo MA, Garcia-Segura LM. Role of astrocytes in the neuroprotective actions of 17β-estradiol and selective estrogen receptor modulators. Mol Cell Endocrinol 2014; 389: 48-57. https://doi.org/10.1016/j.mce.2014.01.009##Arevalo M-A, Santos-Galindo M, Bellini M-J, Azcoitia I, Garcia-Segura L M. Actions of estrogens on glial cells: implications for neuroprotection. Biochim Biophys Acta Gen Subj 2010; 1800: 1106-12. https://doi.org/10.1016/j.bbagen.2009.10.002##Bartley E, Fillingim R. Sex differences in pain: A brief review of clinical and experimental findings. Surv Anesthesiol 2016; 60: 175-6. https://doi.org/10.1097/01.sa.0000484819.20819.8b##Bartley EJ, Fillingim RB. Sex differences in pain: a brief review of clinical and experimental findings. Br J Anaesth 2013; 111: 52-8. https://doi.org/10.1093/bja/aet127##Chambel SS, Tavares I, Cruz CD. Chronic Pain After Spinal Cord Injury: Is There a Role for Neuron-Immune Dysregulation? Front Physiol 2020; 11: 748.##Detloff MR, Fisher LC, McGaughy V, Longbrake EE, Popovich PG, Basso DM. Remote activation of microglia and pro-inflammatory cytokines predict the onset and severity of below-level neuropathic pain after spinal cord injury in rats. Exp Neurol 2008; 212: 337-47. https://doi.org/10.1016/j.expneurol.2008.04.009##Fillingim RB, King CD, Ribeiro-Dasilva MC, Rahim-Williams B, Riley III JL. Sex, gender, and pain: a review of recent clinical and experimental findings. J Pain 2009; 10: 447-85. https://doi.org/10.1016/j.jpain.2008.12.001 ##Gao Y-J, Ji R-R. Targeting astrocyte signaling for chronic pain. Neurotherapeutics 2010; 7: 482-93. https://doi.org/10.1016/j.nurt.2010.05.016##Gaudet AD, Ayala MT, Schleicher WE, Smith EJ, Bateman EM, Maier SF, et al. Exploring acute-to-chronic neuropathic pain in rats after contusion spinal cord injury. Exp Neurol 2017; 295: 46-54. https://doi.org/10.1016/j.expneurol.2017.05.011##Gaudet AD, Fonken LK. Glial cells shape pathology and repair after spinal cord injury. Neurotherapeutics 2018; 15: 554-77. https://doi.org/10.1007/s13311-018-0630-7##Gupta DS, Hubscher CH. Estradiol treatment prevents injury induced enhancement in spinal cord dynorphin expression. Front Physiol 2012; 3: 28.##Hadjimarkou MM, Vasudevan N. GPER1/GPR30 in the brain: Crosstalk with classical estrogen receptors and implications for behavior. J Steroid Biochem Mol 2018; 176: 57-64. https://doi.org/10.1016/j.jsbmb.2017.04.012##Hains BC, Waxman SG. Activated microglia contribute to the maintenance of chronic pain after spinal cord injury. J Neurosci 2006; 26: 4308-17. https://doi.org/10.1523/JNEUROSCI.0003-06.2006##Hains BC, Yucra JA, Hulsebosch CE. Reduction of pathological and behavioral deficits following spinal cord contusion injury with the selective cyclooxygenase-2 inhibitor NS-398. J Neurotrauma 2001; 18: 409-23. https://doi.org/10.1089/089771501750170994##Hulsebosch CE, Hains BC, Crown ED, Carlton SM. Mechanisms of chronic central neuropathic pain after spinal cord injury. Brain Res Rev 2009; 60: 202-13. https://doi.org/10.1016/j.brainresrev.2008.12.010##Ji R-R, Donnelly CR, Nedergaard M. Astrocytes in chronic pain and itch. Nat Rev Neurosci 2019; 20: 667-85. https://doi.org/10.1038/s41583-019-0218-1 ##Kawasaki Y, Zhang L, Cheng J-K, Ji R-R. Cytokine mechanisms of central sensitization: distinct and overlapping role of interleukin-1β, interleukin-6, and tumor necrosis factor-α in regulating synaptic and neuronal activity in the superficial spinal cord. J Neurosci 2008; 28: 5189-94. https://doi.org/10.1523/JNEUROSCI.3338-07.2008##Kim HW, Won CH, Oh SB. Lack of correlation between spinal microgliosis and long-term development of tactile hypersensitivity in two different sciatic nerve crush injury. Mol Pain 2021; 17: 17448069211011326. https://doi.org/10.1177/17448069211011326##Kuo J, Hamid N, Bondar G, Dewing P, Clarkson J, Micevych P. Sex differences in hypothalamic astrocyte response to estradiol stimulation. Biol Sex Differ 2010; 1: 7. https://doi.org/10.1186/2042-6410-1-7  ##Mousavi Z, Shafaghi B, Kobarfard F, Jorjani M. Sex differences and role of gonadal hormones on glutamate level in the nucleus accumbens in morphine tolerant rats: a microdialysis study. Eur J Pharmacol 2007; 554: 145-9. https://doi.org/10.1016/j.ejphar.2006.10.010##Nag S, Mokha S S. Testosterone is essential for α2-adrenoceptor-induced antinociception in the trigeminal region of the male rat. Neurosci Lett 2009; 467: 48-52. https://doi.org/10.1016/j.neulet.2009.10.016##Naseri K, Saghaei E, Abbaszadeh F, Afhami M, Haeri A, Rahimi F, et al. Role of microglia and astrocyte in central pain syndrome following electrolytic lesion at the spinothalamic tract in rats. J Mol Neurosci 2013; 49: 470-9. https://doi.org/10.1007/s12031-012-9840-3 ##Naseri K, Saghaei E, Abbaszadeh F, Afhami M, Haeri A, Jorjani M. The effect of estradiol on astrogliosis related to central pain syndrome after spinal cord injury in male rat. 14th World Congress on Pain, Milan, Italy 2012. ##Okada-Ogawa A, Suzuki I, Sessle BJ, Chiang C-Y, Salter MW, Dostrovsky JO, et al. Astroglia in medullary dorsal horn (trigeminal spinal subnucleus caudalis) are involved in trigeminal neuropathic pain mechanisms. J Neurosci 2009; 29: 11161-71. https://doi.org/10.1523/JNEUROSCI.3365-09.2009 ##Oyinbo CA. Secondary injury mechanisms in traumatic spinal cord injury: a nugget of this multiply cascade. Acta Neurobiol Exp (Wars) 2011; 71: 281-99. ##Parducz A, Hajszan T, Maclusky N, Hoyk Z, Csakvari E, Kurunczi A, et al. Synaptic remodeling induced by gonadal hormones: neuronal plasticity as a mediator of neuroendocrine and behavioral responses to steroids. Neuroscience 2006; 138: 977-85. https://doi.org/10.1016/j.neuroscience.2005.07.008 ##Ren K. An improved method for assessing mechanical allodynia in the rat. Physiol Behav 1999; 67: 711-6. https://doi.org/10.1016/S0031-9384(99)00136-5##Saghaei E, Abbaszadeh F, Naseri K, Ghorbanpoor S, Afhami M, Haeri A, et al. Estradiol attenuates spinal cord injury-induced pain by suppressing microglial activation in thalamic VPL nuclei of rats. Neurosci Res 2013; 75: 316-23. https://doi.org/10.1016/j.neures.2013.01.010##Schreiber KL, Beitz AJ, Wilcox GL. Activation of spinal microglia in a murine model of peripheral inflammation-induced, long-lasting contralateral allodynia. Neurosci Lett 2008; 440: 63-7. https://doi.org/10.1016/j.neulet.2008.05.044##Sengelaub DR, Han Q, Liu N-K, Maczuga MA, Szalavari V, Valencia SA, et al. Protective effects of estradiol and dihydrotestosterone following spinal cord injury. Journal of neurotrauma 2018; 35: 825-41. https://doi.org/10.1089/neu.2017.5329 ##Shiao R, Lee-Kubli CA. Neuropathic pain after spinal cord injury: challenges and research perspectives. Neurotherapeutics 2018; 15: 635-53. https://doi.org/10.1007/s13311-018-0633-4  ##Sipski M L, Jackson AB, Gómez-Marín O, Estores I, Stein A. Effects of gender on neurologic and functional recovery after spinal cord injury. Arch Phys Med Rehabil 2004; 85: 1826-36. https://doi.org/10.1016/j.apmr.2004.04.031  ##Sorge RE, Mapplebeck JC, Rosen S, Beggs S, Taves S, Alexander JK, et al. Different immune cells mediate mechanical pain hypersensitivity in male and female mice. Nat Neurosci 2015; 18: 1081-3. https://doi.org/10.1038/nn.4053##Sribnick EA, Wingrave JM, Matzelle DD, Wilford GG, Ray SK, Banik NL. Estrogen attenuated markers of inflammation and decreased lesion volume in acute spinal cord injury in rats. J Neurosci Res 2005; 82: 283-93. https://doi.org/10.1002/jnr.20622 ##Tran AP, Warren PM, Silver J. The biology of regeneration failure and success after spinal cord injury. Physiol Rev 2018; 98: 881-917. https://doi.org/10.1152/physrev.00017.2017##Traub RJ, Ji Y. Sex differences and hormonal modulation of deep tissue pain. Front Neuroendocrinol 2013; 34: 350-66. https://doi.org/10.1016/j.yfrne.2013.07.002##Wang G, Thompson SM. Maladaptive homeostatic plasticity in a rodent model of central pain syndrome: thalamic hyperexcitability after spinothalamic tract lesions. J Neurosci 2008; 28: 11959-69. https://doi.org/10.1523/JNEUROSCI.3296-08.2008 ##Watson JL, Hala TJ, Putatunda R, Sannie D, Lepore AC. Persistent at-level thermal hyperalgesia and tactile allodynia accompany chronic neuronal and astrocyte activation in superficial dorsal horn following mouse cervical contusion spinal cord injury. PLoS One 2014; 9: e109099. ##Yezierski RP. Pain following spinal cord injury: pathophysiology and central mechanisms. Prog Brain Res Vol 129: Elsevier, 2000: 429-49.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of cinnamon on antioxidant content and ZO-1 gene expression in the brain following middle cerebral artery occlusion in rats receiving high-fatdiet</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Despite all the research, no definitive treatment for stroke has been found yet. Cinnamon is a plant that has been shown to have health benefits effects. In this study, the effect of pretreatment of cinnamon on ischemia tolerance and the expression of Zonula occludens 1(ZO-1) gene in the brains of rats receiving a high-fat diet was investigated.
Methods: In this study, 72 rats were divided into six groups: control, sham, model (stroke), vehicle, lovastatin, and cinnamon. All groups except the control group received a high-fat diet for 8 weeks. Then the last three groups received Carboxymethyl cellulose, lovastatin, and cinnamon 130 mg accordingly for 6 weeks. Stroke was induced by middle cerebral artery occlusion (MCAO). Twelve hours later, the animals were examined for the extent of serum lipids, brain edema, anti-oxidant capacity and gene expression of ZO-1.
Results: Cinnamon was effective in reducing serum cholesterol and triglyceride. Cinnamon treatment significantly diminished brain edema. It also restored anti-oxidant capacity. ZO-1 gene expression was increased in the ischemic brains after cinnamon treatment (P&#60; 0.05).
Conclusion: Pretreatment with Cin130 had beneficial effects on the serum lipid profile, edema volume in ischemic brain and anti-oxidant capacity. It increased ZO-1 gene expression and so maintained cellular integrity and prevented the subsequent edema.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>42</FPAGE>
			<TPAGE>52</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/29
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/4/8
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/28
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/9/7
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Hossein</Name>
				<MidName></MidName>
				<Family>Mostafavi</Family>
				<NameE>Hossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mostafavi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Massoud</Name>
				<MidName></MidName>
				<Family>Hatami</Family>
				<NameE>Massoud</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hatami</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohsen</Name>
				<MidName></MidName>
				<Family>Alipour</Family>
				<NameE>Mohsen</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alipour</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Seyyed Saeid</Name>
				<MidName></MidName>
				<Family>Mousavi</Family>
				<NameE>Seyyed Saeid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mousavi</FamilyE>
				<Organizations>
				<Organization>Animal Science Research Department, Zanjan Agricultural and Natural Recourses Research and Education Centrer, AREEO, Zanjan, Iran *</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hadi</Name>
				<MidName></MidName>
				<Family>Feizi</Family>
				<NameE>Hadi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Feizi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hfeizik@zums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Stroke</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cinnamon</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>MCAO</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Brain edema</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>ZO-1.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abdelnour, L. and F. El-Nagi (2017). Functional Neurological Disorder Presenting as Stroke: A Narrative Review. J Psychol Abnorm 6(159): 2.##Adibhatla R. M and H. J. F. (2008). Phospholipase A2, Reactive Oxygen Species, and Lipid Peroxidation In CNS pathologies. BMB Rep. 41(8): 560-567.##Aebi, H. (1984). [13] Catalase in vitro. Methods in enzymology 105: 121-126.##Anderson, R. A., Z. Zhan, R. Luo, X. Guo, Q. Guo, J. Zhou, J. Kong, P. A. Davis and B. J. Stoecker (2016). Cinnamon extract lowers glucose, insulin and cholesterol in people with elevated serum glucose. J Tradit Complement Med 6(4): 332-336.##Andreadou, I., E. K. Iliodromitis, D. Farmakis and D. T. Kremastinos (2009). To prevent, protect and save the ischemic heart: antioxidants revisited. Expert Opin Ther Targets 13(8): 945-956.##Babu, P. S., S. Prabuseenivasan and S. Ignacimuthu (2007). Cinnamaldehyde-a potential antidiabetic agent. Phytomedicine 14(1): 15-22.##Beji, R. S., S. Khemir, W. A. Wannes, K. Ayari and R. Ksouri (2018). Antidiabetic, antihyperlipidemic and antioxidant influences of the spice cinnamon (Cinnamomum zeylanicumon) in experimental rats. Brazilian Journal of Pharmaceutical Sciences 54(2).##Campbell, B. C. V., D. A. De Silva, M. R. Macleod, S. B. Coutts, L. H. Schwamm, S. M. Davis and G. A. Donnan (2019). Ischaemic stroke. Nat Rev Dis Primers 5(1): 70. 10.1038/s41572-019-0118-8##Chen, Y.-F., Y.-W. Wang, W.-S. Huang, M.-M. Lee, W. G. Wood, Y.-M. Leung and H.-Y. Tsai (2016). Trans-cinnamaldehyde, an essential oil in cinnamon powder, ameliorates cerebral ischemia-induced brain injury via inhibition of neuroinflammation through attenuation of iNOS, COX-2 expression and NFκ-B signaling pathway. Neuromolecular medicine 18(3): 322-333.##Farhoudi M, Mehrvar K, Sadeghi-Bazargani H, Hashemilar M, Seyedi-Vafaee M, Sadeghi-Hokmabad E, Rikhtegar R, Saber-Maroof B, Abutalebi M, Rezaei M, Vaferi S, Aghili A and E. O (2017). Stroke subtypes, risk factors and mortality rate in northwest of Iran. Iran J Neurol. 16(3): 112-117.##Frydman-Marom, A., A. Levin, D. Farfara, T. Benromano, R. Scherzer-Attali, S. Peled, R. Vassar, D. Segal, E. Gazit, D. Frenkel and M. Ovadia (2011). Orally Administrated Cinnamon Extract Reduces β-Amyloid Oligomerization and Corrects Cognitive Impairment in Alzheimer's Disease Animal Models. PLoS One 6(1).##G Y Yang and A L Betz (1994). Reperfusion-Induced Injury to the Blood-Brain Barrier After Middle Cerebral Artery Occlusion in Rats. Stroke 25(8): 1658-1664.##Ghosh T, Basu A, Adhikari D, Roy D and Pal A.K (2015). Antioxidant activity and structural features of Cinnamomum zeylanicum. 3 Biotech. Dec; 5(6): 939-947.##Giustarini, D., I. Dalle-Donne, D. Tsikas and R. Rossi (2009). Oxidative stress and human diseases: Origin, link, measurement, mechanisms, and biomarkers. Crit Rev Clin Lab Sci 46(5-6): 241-281.##Hosseini A A, Sobhani-Rad D, Ghandehari K and Benamer H (2010). Frequency and clinical patterns of stroke in Iran - Systematic and critical review. BMC Neurol 10(72).##Ighodaro, O. M. and O. A. Akinloye (2018). First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alexandria Journal of Medicine 54(4): 287-293.##Jana, A., K. K. Modi, A. Roy, J. A. Anderson, R. B. van Breemen and K. Pahan (2013). Up-regulation of neurotrophic factors by cinnamon and its metabolite sodium benzoate: Therapeutic implications for neurodegenerative disorders. J Neuroimmune Pharmacol 8(3): 739-755.##Jiao, H., Z. Wang, Y. Liu, P. Wang and Y. Xue (2011). Specific role of tight junction proteins claudin-5, occludin, and ZO-1 of the blood-brain barrier in a focal cerebral ischemic insult. J Mol Neurosci 44(2): 130-139.##Kalogeris T, Baines CP, Krenz M and Korthuis RJ (2016). Ischemia/Reperfusion. Compr Physiol. 6(7(1)): 113-170.##Kalogeris, T., Y. Bao and R. J. Korthuis (2014).Mitochondrial reactive oxygen species: a double edged sword in ischemia/reperfusion vs preconditioning. Redox Biol 2: 702-714.##Lewis A and S. A. (2010). Hyperlipidemia and primary prevention of stroke: does risk factor identification and reduction really work? Curr Atheroscler Rep. Jul;12(4): 225-229.##Longa EZ, Weinstein PR, Carlson S and Cummins R (1989). Reversible middle cerebral artery occlusion without craniectomy in rats. Stroke 20: 84-91.##Luissint, A.-C., C. Artus, F. Glacial, K. Ganeshamoorthy, P.-O. J. F. Couraud and B. o. t. CNS (2012). Tight junctions at the blood brain barrier: physiological architecture and disease-associated dysregulation. Fluids Barriers CNS. 9(1): 23.##Marques C, Meireles M, Norberto S, Leite J, Freitas J, Pestana D, Faria A and C. C. (2015). High-fat diet-induced obesity Rat model: a comparison between Wistar and Sprague-Dawley Rat. Adipocyte. Jul 15(5(1)): 11-21.##McCord, J. M. and I. Fridovich (1969). Superoxide dismutase: an enzymic function for erythrocuprein (hemocuprein). Journal of Biological chemistry 244(22): 6049-6055.##Mirhadi, K. (2011). Effect of Intraperitoneally Injection of Different Doses of Lovastatin on Pain and Inflammatory Response Induced by Formalin in Mice  American Journal of Animal and Veterinary Sciences 6(4): 160-165.##Moradi, P., M. Ganjkhani, I. J. Anarkooli and A. Abdanipour (2019). Neuroprotective effects of lovastatin in the pilocarpine rat model of epilepsy according to the expression of neurotrophic factors. Metabolic brain disease 34(4): 1061-1069.##Nelson., R. H. ( 2013). Hyperlipidemia as a Risk Factor for Cardiovascular Disease. Prim Care. Mar; 40(1): 195-211.##Panahpour, H., A. A. Nekooeian and G. A. Dehghani (2014). Candesartan attenuates ischemic brain edema and protects the blood-brain barrier integrity from ischemia/reperfusion injury in rats. Iranian biomedical journal 18(4): 232.##Panickar, K. S. and R. A. Anderson (2011). Effect of polyphenols on oxidative stress and mitochondrial dysfunction in neuronal death and brain edema in cerebral ischemia. Int J Mol Sci 12(11): 8181-8207.##R Buettner, K G Parhofer, M Woenckhaus, C E Wrede, L A Kunz-Schughart, J Schölmerich and L. C. Bollheimer (2006). Defining high-fat-diet rat models: metabolic and molecular effects of different fat types. J Mol Endocrinol 2006 Jun;36(3):485-501.##Ranasinghe, P., S. Perera, M. Gunatilake, E. Abeywardene, N. Gunapala, S. Premakumara, K. Perera, D. Lokuhetty and P. Katulanda (2012). Effects of Cinnamomum zeylanicum (Ceylon cinnamon) on blood glucose and lipids in a diabetic and healthy rat model. Pharmacognosy Res 4(2): 73-79.##Rao PV and G. SH. (2014). Cinnamon: a multifaceted medicinal plant. Evidence-Based Complementary and Alternative Medicine 2014: 642942.##Rempe R. G, Hartz A. MS and B. B (2016). Matrix metalloproteinases in the brain and blood-brain barrier: Versatile breakers and makers. J Cereb Blood Flow Metab. 36(9): 1481-1507.##Sedighi M, Bahmani M, Asgary S, Beyranvand F and R.-K. M. (2017). A review of plant based compounds and medicinal plants effective on atherosclerosis. J Res Med Sci 22(30).##Stavinoha R. C and D. A. Vattem (2015). Potential neuroprotective effects of cinnamon  International Journal of Applied Research in Natural Products 8(3): 24-46.##Sun M-Sh, Jin H, Sun X, Huang Sh, Zhang Fu-L, Guo Zh-Ni and Yang Y (2018). Free Radical Damage in Ischemia-Reperfusion Injury: An Obstacle in Acute Ischemic Stroke after Revascularization Therapy. Oxidative Medicine and Cellular Longevity: 17 pages.##Tan, B. L. and M. E. Norhaizan (2019). Effect of High-Fat Diets on Oxidative Stress, Cellular Inflammatory Response and Cognitive Function. Nutrients 11(11): 2579.##Tuzcu Z, Orhan C, Sahin N, Juturu V and Sahin K (2017). Cinnamon Polyphenol Extract Inhibits Hyperlipidemia and Inflammation by Modulation of Transcription Factors in High-Fat Diet-Fed Rats. Oxidative Medicine and Cellular Longevity 2017: 10 pages.##Vafa, M., F. Mohammadi, F. Shidfar, M. S. Sormaghi, I. Heidari, B. Golestan and F. Amiri (2012). Effects of cinnamon consumption on glycemic status, lipid profile and body composition in type 2 diabetic patients. Int J Prev Med 3(8): 531-536.##Verspohl EJ, Bauer K and N. E. (2005). Antidiabetic effect of Cinnamomum cassia and Cinnamomum zeylanicum in vivo and in vitro. Phytother Res. Mar;19(3): 203-206.##Xue, R., J. Lv, J. Gao, R. Fu, W. Li, X. Lei, G. Wu, L. Xue and Z. Zhang (2013). Protective effect of tea polyphenols on the blood-brain barrier. Translational Neuroscience 4(3): 295-301.##Yulug, B., E. Kilic, S. Altunay, C. Ersavas, C. Orhan, A. Dalay, M. Tuzcu, N. Sahin, V. Juturu and K. Sahin (2018). Cinnamon Polyphenol Extract Exerts Neuroprotective Activity in Traumatic Brain Injury in Male Mice. CNS Neurol Disord Drug Targets 17(6): 439-447.##Zeljkovic, A., J. Vekic, V. Spasojevic-Kalimanovska, Z. Jelic-Ivanovic, N. Bogavac-Stanojevic, B. Gulan and S. Spasic (2010). LDL and HDL subclasses in acute ischemic stroke: prediction of risk and short-term mortality. Atherosclerosis 210(2): 548-554.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Azadirachta indica A. Juss flower extract attenuates memory deficit induced by restraint stress in malerats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Chronic stress is related to cognitive impairment. Azadirachta indica A. Juss. (A. indica) leaf extract possesses antioxidant and cognitive enhancement effects. Therefore, this study was set up to evaluate the cognitive-enhancing effects of A. indica flower extract in stressed rats.
Methods: Male Wistar rats were randomly divided into control and stress groups. Restraint stress was induced to stress groups 3 h daily. The stressed rats were given vehicles, donepezil (a positive control meditation used to improve cognition), and A. indica at 250, 500, and 1000 mg/kg BW for 30 days. The novel object recognition test (NORT) was used to assess cognitive function, and the open field test (OFT) was utilized to assess spontaneous locomotor activity. Their brains and blood were taken to measure levels of brain-derived neurotrophic factor (BDNF), blood cortisol levels, and the density of survival neurons.
Results: The discrimination index ratio of the stressed rats treated with either donepezil or A. indica flower extract at all doses was significantly improved as measured by NORT. Moreover, there was no significant difference between the control and stress groups in the locomotor behaviors of rearing and number of crossing. The stressed rats treated with donepezil and A. indica flower extract had significantly higher BDNF levels and also survival neuron density in the brain. However, their blood cortisol levels were lower than the stressed rats given the vehicle.
Conclusion: A. indica flower extract helps improve cognitive function in stressed rats by boosting BDNF and protecting against neuronal loss in the brain.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>53</FPAGE>
			<TPAGE>63</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/292021/11/11
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/8/20
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/282022/04/11
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/1/22
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Thaneeya</Name>
				<MidName></MidName>
				<Family>Hawiset</Family>
				<NameE>Thaneeya</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hawiset</FamilyE>
				<Organizations>
				<Organization>School of Medicine, Mae Fah Luang University, Muang, Chiang Rai, 57100, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email>thaneeya.haw@mfu.ac.th</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Napatr</Name>
				<MidName></MidName>
				<Family>Sriraksa</Family>
				<NameE>Napatr</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sriraksa</FamilyE>
				<Organizations>
				<Organization>School of Medical Sciences, University of Phayao, Muang, Phayao, 56000, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ratchaniporn</Name>
				<MidName></MidName>
				<Family>Kongsui</Family>
				<NameE>Ratchaniporn</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kongsui</FamilyE>
				<Organizations>
				<Organization>School of Medical Sciences, University of Phayao, Muang, Phayao, 56000, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Utcharaporn</Name>
				<MidName></MidName>
				<Family>Kamsrijai</Family>
				<NameE>Utcharaporn</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kamsrijai</FamilyE>
				<Organizations>
				<Organization>School of Medicine, Mae Fah Luang University, Muang, Chiang Rai, 57100, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Keerati</Name>
				<MidName></MidName>
				<Family>Wanchai</Family>
				<NameE>Keerati</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Wanchai</FamilyE>
				<Organizations>
				<Organization>School of Medicine, Mae Fah Luang University, Muang, Chiang Rai, 57100, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Prachak</Name>
				<MidName></MidName>
				<Family>Inkaew</Family>
				<NameE>Prachak</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Inkaew</FamilyE>
				<Organizations>
				<Organization>School of Science, Mae Fah Luang University, Muang, Chiang Rai, 57100, Thailand</Organization>
				</Organizations>
				<Countries>
				<Country>Thailand</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Azadirachta indica A. Juss.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Memory</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Restraint stress</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>BDNF</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Survival neuron density</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Alzohairy MA. Therapeutics role of Azadirachta indica (Neem) and their active constituents in diseases prevention and treatment. Evid Based Complement Alternat Med 2016; 2016: 7382506.##Ávila-Villanueva M, Gómez-Ramírez J, Maestú F, Venero C, Ávila J, Fernández-Blázquez MA. The role of chronic stress as a trigger for the Alzheimer disease continuum. Front Aging Neurosci 2020; 12: 561504.##Behl C, Lezoualc’h F, Trapp T, Widmann M, Skutella T, Holsboer F. Glucocorticoids enhance oxidative stress-induced cell death in hippocampal neurons in vitro. Endocrinology 1997; 138: 101-6.##Borwicka C, Lala R, Limb LW, Stagg CJ, Aquilia L. Dopamine depletion effects on cognitive flexibility as modulated by tDCS of the dlPFC. Brain Stimulation 2020; 13(1): 105-8.##Chaisawangwong W, Gritsanapan W. Extraction method for high free radical scavenging activity of Siamese neem tree flowers. Songklanakarin J Sci Technol 2009; 31: 419-23.##Chen H, Lombès M, Le Menuet D. Glucocorticoid receptor represses brain-derived neurotrophic factor expression in neuron-like cells. Mol Brain 2017; 12; 1-16.##Dayi A, Cetin F, Sisman AR, Aksu I, Tas A, Gönenc S, Uysal N. The effects of oxytocin on cognitive defect caused by chronic restraint stress applied to adolescent rats and on hippocampal VEGF and BDNF levels. Med Sci Monit 2015; 21: 69-75.##de Boer VCJ, Dihal AA, van der Woude H, Arts ICW, Wolffram S, Alink GM, et al. Tissue distribution of quercetin in rats and pigs. J Nutr 2005; 135: 1718-25.##de Kloet ER, Oitzl MS, Joëls M. Stress and cognition: are corticosteroids good or bad guys? Trends Neurosci 1999; 22, 422-6.##Djavadian RL. Serotonin and neurogenesis in the hippocampal dentate gyrus of adult mammals. Acta Neurobiol Exp 2004; 64: 189-200.##Duangjai A, Nuengchanong N, Lee LH, Goh BH, Sakaew S, Suphrom N. Characterisation of an extract and fractions of Azadirachta indica flower on cholesterol lowering property and intestinal motility. Nat Prod Res 2019; 33: 1491-4##Eid A, Jaradat N, Elmarzugi N. A review of chemical constituents and traditional usage of Neem plant (Azadirachta indica). Pal Med Pharm J 2017; 2: 75-81.##Hall CS. Emotional behavior in the rat. I. Defecation and urination as measures of individual differences in emotionality. J Comp Psychol 1934; 18: 385-403.##Hawiset T, Sriraksa N, Kamsrijai U, Wanchai K, Inkaew P. Anxiolytic and antidepressant-like activities of aqueous extract of Azadirachta indica A. Juss. flower in the stressed rats. Heliyon 2022; 8: e08881.##Huang EJ, Reichardt LF. Neurotrophins: roles in neuronal development and function. Ann Rev Neurosci 2001; 24: 677-736.##Husain M, Mehta MA. Cognitive enhancement by drugs in health and disease. Trends Cogn Sci 2011; 15: 28-36.##Jaiswal AK, Bhattacharya SK, Acharya SB. Anxiolytic activity of Azadirachta indica leaf extract in rats. Indian J Exp Biol 1994; 32: 489-91.##Jenkins TA, Nguyen JCD, Polglaze KE, Bertrand PP. Influence of tryptophan and serotonin on mood and cognition with a possible role of the gut-brain axis. Nutrients 2016; 8: 56.##Khan S, Khan RA. Chronic stress leads to anxiety and depression. Ann Psychiatry Mental Health 2017; 5: 1091.##Kim JJ, Diamond DM. The stressed hippocampus, synaptic plasticity and lost memories. Nat Rev Neurosci 2002; 3: 453-62.##Kumar A, Rinwa P, Kaur G, Machawal L. Stress: Neurobiology, consequences and management. J Pharm Bioallied Sci 2013; 5: 91-7.##Li Y, Zhou S, Li J, Sun Y, Hasimu H, Liu R, Zhang T. Quercetin protects human brain microvascular endothelial cells from fibrillar β-amyloid1-40-induced toxicity. Acta Pharm Sin B 2015; 5: 47-54.##Lin J, Huang L, Yu J, Xiang S, Wang J, Zhang J, et al. Fucoxanthin, a marine carotenoid, reverses scopolamine-induced cognitive impairments in mice and inhibits acetylcholinesterase in vitro. Mar drugs 2016; 14: 67.##Lupien SJ, McEwen BS. The acute effects of corticosteroids on cognition: Integration of animal and human model studies. Brain Res Rev 1997; 24: 1-27.##Martinowich K, Lu B. Interaction between BDNF and serotonin: role in mood disorders. Neuropsychopharmacology 2008; 33: 73-83.##McEwen BS, Nasca C, Gray JD. Stress effects on neuronal structure: hippocampus, amygdala, and prefrontal cortex. Neuropsychopharmacology 2016; 41: 3-23.##McLaughlin KJ, Gomez JL, Baran E, Conrad CD. The effects of chronic stress on hippocampal morphology and function: an evaluation of chronic restraint paradigms. Brain Res 2007; 1161: 56-64.##Miranda M, Morici JF, Zanoni MB, Bekinschtein P. Brain-derived neurotrophic factor: a key molecule for memory in the healthy and the pathological brain. Front Cell Neurosci 2019; 13: 363.##Mohammadi HS, Goudarzi I, Lashkarbolouki T, Abrari K, Salmani ME. Chronic administration of quercetin prevent spatial learning and memory deficits provoked by chronic stress in rats. Behav Brain Res 2014; 270: 196-205.##Nakagawa T, Ohta K. Quercetin regulates the integrated stress response to improve memory. Int J Mol Sci 2019; 20: 2761.##Numakawa T, Odaka H, Adachi N. Actions of brain-derived neurotrophin factor in the neurogenesis and neuronal function, and its involvement in the pathophysiology of brain diseases. Int J Mol Sci 2018; 19: 3650.##Ohira K. Dopamine as a growth differentiation factor in the mammalian brain. Int J Mol Sci 2017; 18: 2312.##Ortiz JB, Mathewson CM, Hoffman AN, Hanavan PD, Terwilliger EF, Conrad CD. Hippocampal brain-derived neurotrophic factor mediates recovery from chronic stress-induced spatial reference memory deficits. Eur J Neurosci 2014; 40: 3351-3362.##Paxinos G, Watson C, editors. The rat brain in stereotaxic coordinates. United States of America: Academic Press, Inc., 1997, p. 55.##Raghavendra M, Maiti R, Kumar S, Acharya SB. Role of aqueous extract of Azadirachta indica leaves in an experimental model of Alzheimer’s disease in rats. Int J Appl Basic Med Res 2013; 3: 37-47.##Ren S, Suo Q, Du W, Pan H, Yang M, Wang R, et al. Quercetin permeability across blood-brain barrier and its effect on the viability of U251 cells. J Sichuan Univ 2010; 41: 751-9.##Sahin E, Gümüslü S. Immobilization stress in rat tissues: alterations in protein oxidation, lipid peroxidation and antioxidant defense system. Comp Biochem Physiol C Toxicol Pharmacol 2007; 144: 342-7.##Salleh MR. Life Event, Stress and Illness. Malays J Med Sci 2008; 15: 9-18.##Samad N, Saleem A, Yasmin F, Shehzad MA. Quercetin protects against stress-induced anxiety- and depression-like behavior and improves memory in male mice. Physiol Res 2018; 67: 795-808.##Sandi C, Pinelo-Nava MT. Stress and Memory: Behavioral effects and neurobiological mechanisms. Neural Plast 2007; 2007: 78970.##Sen P, Mediratta PK, Ray A. Effects of Azadirachta indica A Juss on some biochemical, immunological and visceral parameters in normal and stressed rats. Indian J Exp Biol 1992; 30: 1170-5.##Shirai M, Kawai Y, Yamanishi R, Kinoshita T, Chuman H, Terao J. Effect of a conjugated quercetin metabolite, quercetin 3-glucuronide, on lipid hydroperoxide-dependent formation of reactive oxygen species in differentiated PC-12 cells. Free Radic Res 2006; 40: 1047-53.##Smith MA, Makino S, Kvetnansky R, Post RM. Stress and glucocorticoids affect the expression of brain-derived neurotrophic factor and neurotrophin-3 mRNAs in the hippocampus. J Neurosci 1995; 15: 1768-77.##Sriraksa N, Kongsui R, Thongrong S, Duangjai A, Hawiset T. Effect of Azadirachta indica flower extract on functional recovery of sciatic nerve crush injury in rat models of DM. Exp Ther Med 2019; 17: 541-50.##Stier A, Schull Q, Bize P, Lefol E, Haussmann M, Roussel D, et al. Oxidative stress and mitochondrial responses to stress exposure suggest that king penguins are naturally equipped to resist stress. Sci Reports 2019; 8545: 1-12.##Sun D, Zhong G, Cao HX, Hu Y, Hong XY, Li T, et al. Repeated restraint stress led to cognitive dysfunction by NMDA receptor-mediated hippocampal CA3 dendritic spine impairments in juvenile sprague-dawley rats. Front Mol Neurosci 2020; 13: 552787.##Thippeswamy BS, Mishra B, Veerapur VP, Gupta G. Anxiolytic activity of Nymphaea alba Linn. in mice as experimental models of anxiety. Indian J Pharmacol 2011; 43: 50-5.##Vellucci SV, Parrott RF, Mimmack ML. Down-regulation of BDNF mRNA, with no effect on trkB or glucocorticoid receptor m RNAs, in the porcine hippocampus after acute dexamethasone treatment. Res Vet Sci 2001; 70: 157-62.##Wang DM, Li SQ, Wu WL, Zhu XY, Wang Y, Yuan HY. Effects of long-term treatment with quercetin on cognition and mitochondrial function in a mouse model of Alzheimer’s disease. Neurochem Res 2014; 39:1533-43.##Wang Y, Kan H, Yin Y, Wu W, Hu W, Wang M, et al. Protective effects of ginsenoside Rg1 on chronic restraint stress induced learning and memory impairments in male mice. Pharmacol Biochem Behav 2014; 120: 73-81.##Wanchai K, Hawiset T, Khumsrijai U, Sriraksa N. Azadirachta indica flower extract attenuates kidney oxidative stress in rat exposed to restraint stress. Thai Pharm. Health Sci J 2021; 16: 380-5.##Woo H, Hong CJ, Jung S, Choe S, Yu SW. Chronic restraint stress induces hippocampal memory deficits by impairing insulin signaling. Mol Brain 2018; 37: 1-13.##Yeh SL, Yeh CL, Chan ST, Chuang CH. Plasma rich in quercetin metabolites induces G2/M arrest by upregulating PPAR-γ expression in human A549 lung cancer cells. Planta Med 2011; 77: 992-8.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Evidence for tissue-specific toxicity of malathion by biochemical biomarkers and histopathological indexin two weeks-treated Wistar rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Malathion (MAL), a kind of organophosphate pesticide (OPs), is one of the oldest phosphoric pesticides used for both domestic and commercial agricultural purposes. However, it possesses adverse effects and organ-specific toxicity for the heart, kidney, and other vertebrate organs. The exact effects of the short-term toxicity of MAL on lipid peroxidation, antioxidant activity, and pro-inflammatory cytokines have not been sufficiently elucidated yet.
Methods: We evaluated lipid peroxidation (MDA level), antioxidant activity [superoxide dismutase (SOD) and catalase (CAT)], tumor necrosis factor alpha (TNF-&#945;), and Interleukin-1 beta (IL-1&#946;) in different tissues of MAL-treated Wistar rats, at doses of 50, 100, and 200 mg/kg.
Results: After 14 days of exposure, CAT and SOD activities and MDA level increased in most tissues. Based on the histopathological results, the liver, kidney, and heart were the most affected, while the testes and lungs showed no damage. Also, increased TNF-&#945; was measured as an inflammatory cytokine compared to untreated rats. IL-1&#946; levels showed a dual response to the toxic effects of MAL, such as an increase in testis, kidney, and lung tissues and reduced in liver, heart, and blood tissues.
Conclusion: The present findings reinforce the concept that MAL can cause tissue-specific damage while enhancing the activity of antioxidant enzymes and reducing cytokine levels.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>64</FPAGE>
			<TPAGE>71</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/292021/11/112021/11/20
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/8/29
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/282022/04/112022/06/18
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/3/28
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Mohammad</Name>
				<MidName></MidName>
				<Family>Kiani</Family>
				<NameE>Mohammad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kiani</FamilyE>
				<Organizations>
				<Organization>Student Research Center Committee, Fasa University of Medical Sciences, Fasa, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hiva</Name>
				<MidName></MidName>
				<Family>Alipanah</Family>
				<NameE>Hiva</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alipanah</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>H.alipanah@fums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Seyed Mohammad</Name>
				<MidName></MidName>
				<Family>Mazloomi</Family>
				<NameE>Seyed Mohammad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mazloomi</FamilyE>
				<Organizations>
				<Organization>Department of Food Hygiene and Quality Control, Faculty of Nutrition and Food Sciences, Shiraz University of Medical Sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Roghayeh</Name>
				<MidName></MidName>
				<Family>Nejati</Family>
				<NameE>Roghayeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nejati</FamilyE>
				<Organizations>
				<Organization>Department of Food Safety and Hygiene, School of Health, Fasa University of Medical Sciences, Fasa, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Amene</Name>
				<MidName></MidName>
				<Family>Nematollahi</Family>
				<NameE>Amene</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nematollahi</FamilyE>
				<Organizations>
				<Organization>Department of Food Safety and Hygiene, School of Health, Fasa University of Medical Sciences, Fasa, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehran</Name>
				<MidName></MidName>
				<Family>Sayadi</Family>
				<NameE>Mehran</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sayadi</FamilyE>
				<Organizations>
				<Organization>Department of Food Safety and Hygiene, School of Health, Fasa University of Medical Sciences, Fasa, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m.sayadi@fums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Organophosphates</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cholinesterase Inhibitors</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Agricultural chemicals</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oxidative stress</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Environmental exposure.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Aebi H. Catalase in vitro. Methods in enzymology. Vol 105: Elsevier, 1984: 121-6.##Ahmed RS, Seth V, Pasha S, Banerjee B. Influence of dietary ginger (Zingiber officinales Rosc) on oxidative stress induced by malathion in rats. Food Chem Toxicol 2000; 38: 443-50.##Akhgari M, Abdollahi M, Kebryaeezadeh A, Hosseini R, Sabzevari O. Biochemical evidence for free radicalinduced lipid peroxidation as a mechanism for subchronic toxicity of malathion in blood and liver of rats. Hum Exp Toxicol 2003; 22: 205-11.##Alluwaimi AM, Hussein Y. Diazinon immunotoxicity in mice: modulation of cytokines level and their gene expression. Toxicology 2007; 236: 123-31.##Anbarkeh FR, Nikravesh MR, Jalali M, Sadeghnia HR, Sargazi Z, Mohammdzadeh L. Single dose effect of diazinon on biochemical parameters in testis tissue of adult rats and the protective effect of vitamin E. Iran J Reprod Med 2014; 12: 731.##Ayub S, Verma J, Das N. Effect of endosulfan and malathion on lipid peroxidation, nitrite and TNF-α release by rat peritoneal macrophages. Int Immunopharmacol 2003; 3: 1819-28.##Badr AM. Organophosphate toxicity: Updates of malathion potential toxic effects in mammals and potential treatments. Environ Sci Pollut Res 2020; 27: 26036-57.##Bradford N. A rapid and sensitive method for the quantitation microgram quantities of a protein isolated from red cell membranes. Anal Biochem 1976; 72: e254.##Brocardo PS, Assini F, Franco JL, Pandolfo P, Müller YM, Takahashi RN, et al. Zinc attenuates malathion-induced depressant-like behavior and confers neuroprotection in the rat brain. Toxicol Sci 2007; 97: 140-8.##Coban FK, Ince S, Kucukkurt I, Demirel HH, Hazman O. Boron attenuates malathion-induced oxidative stress and acetylcholinesterase inhibition in rats. Drug Chem Toxicol 2015; 38: 391-9.##Durak D, Uzun FG, Kalender S, Ogutcu A, Uzunhisarcikli M, Kalender Y. Malathion-induced oxidative stress in human erythrocytes and the protective effect of vitamins C and E in vitro. Environmental Toxicology: Int J 2009; 24: 235-42.##Eddleston M, Buckley NA, Eyer P, Dawson AH. Management of acute organophosphorus pesticide poisoning. Lancet 2008; 371: 597-607.##Edwards FL, Yedjou CG, Tchounwou PB. Involvement of oxidative stress in methyl parathion and parathion-induced toxicity and genotoxicity to human liver carcinoma (HepG2) cells. Environ Toxicol 2013; 28: 342-8.##Flehi-Slim I, Chargui I, Boughattas S, El Mabrouk A, Belaïd-Nouira Y, Neffati F, et al. Malathion-induced hepatotoxicity in male Wistar rats: biochemical and histopathological studies. Environ Sci Pollut Res 2015; 22: 17828-38.##Fortunato JJ, Feier G, Vitali AM, Petronilho FC, Dal-Pizzol F, Quevedo J. Malathion-induced oxidative stress in rat brain regions. Neurochem Res 2006; 31: 671-8.##Gupta VK, Siddiqi NJ, Ojha AK, Sharma B. Hepatoprotective effect of Aloe vera against cartap-and malathion-induced toxicity in Wistar rats. J Cell.Physiol 2019; 234: 18329-43.##Hariri AT, Moallem SA, Mahmoudi M, Memar B, Hosseinzadeh H. Sub-acute effects of diazinon on biochemical indices and specific biomarkers in rats: protective effects of crocin and safranal. Food Chem Toxicol 2010; 48: 2803-8.##Heshmati A, Nili-Ahmadabadi A, Rahimi A, Vahidinia A, Taheri M. Dissipation behavior and risk assessment of fungicide and insecticide residues in grape under open-field, storage and washing conditions. J Clean Prod 2020; 270: 122287.##Ince S, Arslan-Acaroz D, Demirel HH, Varol N, Ozyurek HA, Zemheri F, et al. Taurine alleviates malathion induced lipid peroxidation, oxidative stress, and proinflammatory cytokine gene expressions in rats. Biomed Pharmacother 2017; 96: 263-8.##Jalili C, Farzaei MH, Roshankhah S, Salahshoor MR. Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress. J Lab Physicians 2019; 11: 212-9.##Kruger NJ. The Bradford method for protein quantitation. The protein protocols handbook 2009: 17-24.##Lasram MM, Annabi AB, El Elj N, Selmi S, Kamoun A, El-Fazaa S, et al. Metabolic disorders of acute exposure to malathion in adult Wistar rats. J Hazard Mater 2009; 163: 1052-5.##Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974; 47: 469-74.##Mohammadzadeh L, Hosseinzadeh H, Abnous K, Razavi BM. Neuroprotective potential of crocin against malathion-induced motor deficit and neurochemical alterations in rats. Environ Sci Pollut Res 2018; 25: 4904-14.##Moser VC, Stewart N, Freeborn DL, Crooks J, MacMillan DK, Hedge JM, et al. Assessment of serum biomarkers in rats after exposure to pesticides of different chemical classes. Toxicol Appl Pharmacol 2015; 282: 161-74.##Mostafalou S, Eghbal MA, Nili-Ahmadabadi A, Baeeri M, Abdollahi M. Biochemical evidence on the potential role of organophosphates in hepatic glucose metabolism toward insulin resistance through inflammatory signaling and free radical pathways. Toxicol Ind Health 2012; 28: 840-51.##Ohkawa H, Ohishi W, Yagi K. Colorimetric method for determination of MDA activity. Biochemistry 1979; 95: 351.##Pober J, Min W. Endothelial cell dysfunction, injury and death. Handb Exp Pharmacol 2006: 135-56.##Possamai F, Fortunato J, Feier G, Agostinho F, Quevedo J, Wilhelm Filho D, et al. Oxidative stress after acute and sub-chronic malathion intoxication in Wistar rats. Environ Toxicol Pharmacol 2007; 23: 198-204.##Rahimi A, Heshmati A, Nili-Ahmadabadi A. Changes in pesticide residues in field-treated fresh grapes during raisin production by different methods of drying. Dry Technol 2022; 40: 1715-28.##Tan M-S, Yu J-T, Jiang T, Zhu X-C, Tan L. The NLRP3 inflammasome in Alzheimer’s disease. Mol Neurobiol 2013; 48: 875-82.##Yarsan E, Tanyuksel M, Celik S, Aydin A. Effects of aldicarb and malathion on lipid peroxidation. Bull Environ Contam Toxicol 1999; 63: 575-81.##Zabrodskii P, Maslyakov V, Gromov M. Changes in the function of lymphocytes and cytokine concentration in blood caused by the action of atropine under conditions of acute malathion intoxication. Eksp Klin Farmakol 2015; 78: 20-3.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>N-acetyl cysteine in combination with forelimbs remote ischemic preconditioning improves the contrast-induced nephropathy: an in-vivoexperimental study</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Given some limitations in the efficacy of N-acetyl cysteine (NAC) or remote ischemic preconditioning (RIPC) to prevent contrast-induced nephropathy (CIN), the present study investigated the beneficial effects of NAC alone or in combination with RIPC on CIN prevention.
Methods: Rats were randomly assigned into five groups of eight animals each. Group 1 was sham-operated controls. In group 2, an experimental model of diatrizoate-induced CIN was induced. In groups 3 and 4, NAC (150 mg/kg orally, 24 h before the CIN induction) or RIPC (3 cycles of 4 min/4 min of ischemia and reperfusion in the forelimbs 24 h before the CIN induction) was applied, and both strategies were applied in group 5. 48 hours after the intervention, serum was collected to assess creatinine (Cr) and blood urea nitrogen (BUN) levels. Kidney tissue samples were also kept to evaluate the histology and measure malondialdehyde (MDA) levels and superoxide dismutase (SOD) activity.
Results: Considerable increases in serum Cr (0.82&#177;0.04 vs 0.53&#177;0.03 mg/dl) and BUN (49.87&#177;2.85 vs 22.93&#177;1.11 mg/dl) levels in the CIN group showed renal functional damages compared to the sham group. The morphological changes (2 vs 0 score), increased renal MDA levels (8.11&#177;1.27 vs 3.12&#177;0.52 &#956;mol/100 mg tissue), and decreased renal SOD activity (2.29&#177;0.65 vs 27.32&#177;0.98 U/g tissue) in the CIN group represent a remarkable renal injury and oxidative stress compared to the sham group. The individual use of NAC (serum Cr levels: 0.59&#177;0.01 mg/dl; serum BUN levels: 27.24&#177;1.01 mg/dl; morphological changes: 1 score; renal MDA levels: 4.35&#177;0.58 &#956;mol/100 mg tissue; renal SOD activity: 17.24&#177;1.48 U/g tissue) and RIPC (serum Cr levels: 0.60&#177;0.03 mg/dl; serum BUN levels: 28.78&#177;1.66 mg/dl; morphological changes: 1 score; renal MDA levels: 5.34&#177;0.53 &#956;mol/100 mg tissue; renal SOD activity: 13.11&#177;1.96 U/g tissue) improved all indices above. However, the combination of NAC and RIPC (serum Cr levels: 0.57&#177;0.01 mg/dl; serum BUN levels: 25.32&#177;1.14 mg/dl; morphological changes: 1 score; renal MDA levels: 3.56&#177;0.52 &#956;mol/100 mg tissue; renal SOD activity: 30.54&#177;2.92 U/g tissue) was more effective than other strategies used alone.
Conclusion: The combined use of NAC and RIPC may be more useful in preventing CIN than the individual use of possible additive effects through reducing oxidative stress.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>72</FPAGE>
			<TPAGE>79</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/292021/11/112021/11/202021/08/15
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/5/24
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/282022/04/112022/06/182022/04/30
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/2/10
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Behjat</Name>
				<MidName></MidName>
				<Family>Seifi</Family>
				<NameE>Behjat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Seifi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>b-seifi@tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Vaezi</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Vaezi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehri</Name>
				<MidName></MidName>
				<Family>Kadkhodaee</Family>
				<NameE>Mehri</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kadkhodaee</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farzaneh</Name>
				<MidName></MidName>
				<Family>Kianian</Family>
				<NameE>Farzaneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kianian</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Abdollah</Name>
				<MidName></MidName>
				<Family>Sajedizadeh</Family>
				<NameE>Abdollah</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sajedizadeh</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mina</Name>
				<MidName></MidName>
				<Family>Ranjbaran</Family>
				<NameE>Mina</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ranjbaran</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m-ranjbaran@sina.tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Blood urea nitrogen</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Creatinine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Diatrizoate</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oxidative stress</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Renal injury.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Aboubakr HM, Elzohairy EA, Ali AA, Rashed LA, Elkady NK, Soliman AS. Therapeutic effects of N-acetylcysteine against malathion-induced hepatotoxicity. Egypt J Forensic Sci 2019; 9: 34.##Agmon Y, Peleg H, Greenfeld Z, Rosen S, Brezis M. Nitric oxide and prostanoids protect the renal outer medulla from radiocontrast toxicity in the rat. J Clin Invest 1994; 94: 1069-75. https://doi.org/10.1172/JCI117421##Bafna AA, Shah HC. Remote ischemic preconditioning for prevention of contrast-induced nephropathy–A randomized control trial. Indian Heart J 2020; 72 : 244-7. https://doi.org/10.1016/j.ihj.2020.04.010##Beckett KR, Moriarity AK, Langer JM. Safe use of contrast media: what the radiologist needs to know. Radiographics 2015; 35: 1738-50. https://doi.org/10.1148/rg.2015150033##Damasceno AVBS, Barros CAVd, Percario S, Ribeiro Junior RFG, Monteiro AM, Gouveia EHH, et al. Remote ischemic conditioning protects against testicular ischemia∕reperfusion injury in rats. Acta Cir Bras 2020; 35: e202000203. https://doi.org/10.1590/s0102-865020200020000003##Deng J, Lu Y, Ou J, Shao X, Wang X, Xie H. Remote Ischemic preconditioning reduces the risk of contrast-induced nephropathy in patients with moderate renal impairment undergoing percutaneous coronary angiography: A Meta-Analysis. Kidney Blood Press Res 2020; 45: 549-64. https://doi.org/10.1159/000507330##Dugbartey GJ, Redington AN. Prevention of contrast-induced nephropathy by limb ischemic preconditioning: underlying mechanisms and clinical effects. Am J Physiol Renal Physiol 2018; 314: F319-28. https://doi.org/10.1152/ajprenal.00130.2017##Er F, Nia AM, Dopp H, Hellmich M, Dahlem KM, Caglayan E, et al. Ischemic preconditioning for prevention of contrast medium–induced nephropathy: randomized pilot RenPro Trial (Renal Protection Trial). Circulation 2012; 126: 296-303. https://doi.org/10.1161/CIRCULATIONAHA.112.096370##Esterbauer H, Schaur RJ, Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes. Free Radic Biol Med 1991; 11: 81-128. https://doi.org/10.1016/0891-5849(91)90192-6##Faghfouri AH, Zarezadeh M, Tavakoli-Rouzbehani OM, Radkhah N, Faghfuri E, Kord-Varkaneh H, et al. The effects of N-acetylcysteine on inflammatory and oxidative stress biomarkers: A systematic review and meta-analysis of controlled clinical trials. Eur J Pharmacol 2020; 884: 173368. https://doi.org/10.1016/j.ejphar.2020.173368##Geenen RW, Kingma HJ, van der Molen AJ. Contrast-induced nephropathy: pharmacology, pathophysiology and prevention. Insights Imaging 2013; 4: 811-20. https://doi.org/10.1007/s13244-013-0291-3##Gomes V, de Figueredo CP, Caramori P, Lasevitch R, Bodanese L, Araujo A, et al. N-acetylcysteine does not prevent contrast induced nephropathy after cardiac catheterisation with an ionic low osmolality contrast medium: a multicentre clinical trial. Heart 2005; 91: 774-8. https://doi.org/10.1136/hrt.2004.039636##Haq MFU, Yip CS, Arora P. The conundrum of contrast-induced acute kidney injury. J Thorac Dis 2020; 12: 1721-7. https://doi.org/0.21037/jtd.2019.12.88##Honda T, Hirakawa Y, Nangaku M. The role of oxidative stress and hypoxia in renal disease. Kidney Res Clin Pract 2019; 38: 414-26. https://doi.org/10.23876/j.krcp.19.063##Ighodaro O, Akinloye O. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alexandria J Med 2018; 54: 287-93. https://doi.org/10.1016/j.ajme.2017.09.001##Johnsen J, Pryds K, Salman R, Lofgren B, Kristiansen SB, Botker HE. The remote ischemic preconditioning algorithm: effect of number of cycles, cycle duration and effector organ mass on efficacy of protection. Basic Res Cardiol 2016; 111: 10. https://doi.org/10.1007/s00395-016-0529-6.##Kedrah AE, Ari E, Alahdab Y, Gul CB, Macunluoglu B, Atakan A, et al. Effect of the direct renin inhibitor aliskiren in the prevention of experimental contrast-induced nephropathy in the rat. Kidney Blood Press Res 2012; 35: 425-30. https://doi.org/10.1159/000336104##Kelemen JA, Kaserer A, Jensen KO, Stein P, Seifert B, Simmen HP, et al. Prevalence and outcome of contrast-induced nephropathy in major trauma patients. Eur J Trauma Emerg Surg 2020; 1-7. https://doi.org/10.1007/s00068-020-01496-w##Kianian F, Seifi B, Kadkhodaee M, Sadeghipour HR, Ranjbaran M. Nephroprotection through modifying the apoptotic tnf-α/erk1/2/bax signaling pathway and oxidative stress by long-term sodium hydrosulfide administration in ovalbumin-induced chronic asthma. Immunol Invest 2020; 1-17. https://doi.org/10.1080/08820139.2020.1858860##Kianian F, Seifi B, Kadkhodaee M, Sajedizadeh A, Ahghari P. Protective effects of celecoxib on ischemia reperfusion-induced acute kidney injury: comparing between male and female rats. Iran J Basic Med Sci 2019; 22: 43-8. https://doi.org/10.22038/ijbms.2018.29644.7156##Kiss N, Hamar P. Histopathological evaluation of contrast-induced acute kidney injury rodent models. Biomed Res Int 2016; 2016: 3763250. https://doi.org/10.1155/2016/3763250##Kurtoglu T, Durmaz S, Akgullu C, Gungor H, Eryilmaz U, Meteoglu I, et al. Ozone preconditioning attenuates contrast-induced nephropathy in rats. J Surg Res 2015; 195: 604-11. https://doi.org/10.1016/j.jss.2015.01.0411##Li WH, Wang L, He HY, Chen J, Yu YR. Expression of neutrophil gelatinase‑associated lipocalin in low osmolar contrast‑induced nephropathy in rats and the effect of N‑acetylcysteine. Exp Ther Med 2016; 12: 3175-80. https://doi.org/10.3892/etm.2016.3779##Liu N, Lei R, Tang MM, Cheng W, Luo M, Xu Q, et al. Autophagy is activated to protect renal tubular epithelial cells against iodinated contrast media‑induced cytotoxicity. Mol Med Rep 2017; 16: 8277-82. https://doi.org/10.3892/mmr.2017.7599##Mokhtari V, Afsharian P, Shahhoseini M, Kalantar SM, Moini A. A review on various uses of N-acetyl cysteine. Cell J 2017; 19: 11-7. https://doi.org/10.22074/cellj.2016.4872##Ommati MM, Amjadinia A, Mousavi K, Azarpira N, Jamshidzadeh A, Heidari R. N-acetyl cysteine treatment mitigates biomarkers of oxidative stress in different tissues of bile duct ligated rats. Stress 2020; 1-16. https://doi.org/10.1080/10253890.2020.1777970##Ow CP, Ngo JP, Ullah MM, Hilliard LM, Evans RG. Renal hypoxia in kidney disease: cause or consequence? Acta Physiol 2018; 222: e12999. https://doi.org/10.1111/apha.12999##Paoletti F, Mocali A. Changes in CuZn-superoxide dismutase during induced differentiation of murine erythroleukemia cells. Cancer Res 1988; 48: 6674-7.##Shetty R, Udupa N, Mutalik S, Kulkarni V, Rao V. Mechanisms and therapeutics of n-acetylcysteine: A recent update. RJPT 2019; 12: 2584-8. https://doi.org/10.5958/0974-360X.2019.00434.7##Wang F, Yin J, Lu Z, Zhang G, Li J, Xing T, et al. Limb ischemic preconditioning protects against contrast-induced nephropathy via renalase. EBioMedicine 2016; 9: 356-65. https://doi.org/10.1016/j.ebiom.2016.05.017##Wang JH, Subeq YM, Tsai WC, Lee RP, Hsu BG. Intravenous N-acetylcysteine with saline hydration improves renal function and ameliorates plasma total homocysteine in patients undergoing cardiac angiography. Ren Fail 2008; 30: 527-33. https://doi.org/10.1080/08860220802064754##Zagidullin NS, Dunayeva AR, Plechev VV, Gilmanov AZ, Zagidullin SZ, Er F, et al. Nephroprotective effects of remote ischemic preconditioning in coronary angiography. Clin Hemorheol Microcirc 2017; 65: 299-307. https://doi.org/10.3233/CH-16184##Zhang F, Lu Z, Wang F. Advances in the pathogenesis and prevention of contrast-induced nephropathy. Life Sci 2020; 259: 118379. https://doi.org/10.1016/j.lfs.2020.118379## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Efficient Modified-mRNA Transfection in Neural Stem Cells</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Neural stem cells (NSCs) are multipotent stem cells residing in the central nervous system that is capable of self-renewal to support ongoing requirements for neurogenesis in the adult brain. Since NSCs are considered potential candidate cells for neuro-regenerative medicine, applying safe induction methods for them is very important. Synthetic modified-mRNA (mmRNA) as an alternative to traditional DNA- or protein-based methods, is regarded as a powerful tool for inducing short-term gene expression in cells with no genetic manipulation.
Methods: Here, we aimed to develop an optimized condition for mmRNA transfection in primary NSCs. In vitro-transcribed EGFP mmRNA (mmRNAEGFP) was delivered to human embryonic kidney cells (HEK293T) and mouse NSCs by using two commercial agents, Lipofectamine-2000 (LF2000) and TransIT. Also, a plasmid DNA was used to transfect cells considered EGFP-expressing positive control. In addition, the poly(A) tail (poly adenosine tail) elongation and chloroquine (CQ) treatment were performed to improve transfection efficiency. Finally, flow cytometry, fluorescence microscopy, and MTT assays were performed to assess the cells.
Results: In comparison with HEK293T, NSCs were very sensitive to transfection, the efficacy of transfection using DNA/LF2000 was higher in HEK293T cells, but mmRNAEGFP/ TransIT showed better transfection efficacy in NSCs. Poly(A) tail elongation; also, treating the cells with CQ before transfection significantly improved its efficacy.
Conclusion: The mmRNA poly(A) tail elongation and the use of specific transfection agents in combination with TLR inhibitors can lead to a more effective transfection in NSCs.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>80</FPAGE>
			<TPAGE>91</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/292021/11/112021/11/202021/08/152021/08/24
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/6/2
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/282022/04/112022/06/182022/04/302021/12/4
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/9/13
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Reyhaneh</Name>
				<MidName></MidName>
				<Family>Khayamabed</Family>
				<NameE>Reyhaneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Khayamabed</FamilyE>
				<Organizations>
				<Organization>Department of Biology, ACECR Institute of Higher Education, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Naeimeh</Name>
				<MidName></MidName>
				<Family>Rezaie</Family>
				<NameE>Naeimeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rezaie</FamilyE>
				<Organizations>
				<Organization>Department of Animal Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Elnaz</Name>
				<MidName></MidName>
				<Family>Poorgolizadeh</Family>
				<NameE>Elnaz</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Poorgolizadeh</FamilyE>
				<Organizations>
				<Organization>Department of Biology, ACECR Institute of Higher Education, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farshad</Name>
				<MidName></MidName>
				<Family>Homayouni Moghadam</Family>
				<NameE>Farshad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Homayouni Moghadam</FamilyE>
				<Organizations>
				<Organization>Department of Biology, ACECR Institute of Higher Education, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>homayouni@royan-rc.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Kianoush</Name>
				<MidName></MidName>
				<Family>Dorminani</Family>
				<NameE>Kianoush</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Dorminani</FamilyE>
				<Organizations>
				<Organization>Department of Animal Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Hossein</Name>
				<MidName></MidName>
				<Family>Nasr-Esfahani</Family>
				<NameE>Mohammad Hossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nasr-Esfahani</FamilyE>
				<Organizations>
				<Organization>Department of Animal Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Modified-mRNA</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>In vitro transcription</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Neural stem cell</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Chloroquine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Transfection</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cell culture.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Avci-Adali M, Behring A, Keller T, Krajewski S, Schlensak C, Wendel H P. Optimized conditions for successful transfection of human endothelial cells with in vitro synthesized and modified mRNA for induction of protein expression. Journal of Biological Engineering 2014; 8: 8.##Badieyan Z S, Evans T. Concise review: application of chemically modified mRNA in cell fate conversion and tissue engineering. Stem cells translational medicine 2019; 8: 833-843.##Bell G D, Yang Y, Leung E, Krissansen G W. mRNA transfection by a Xentry-protamine cell-penetrating peptide is enhanced by TLR antagonist E6446. PloS one 2018; 13: e0201464.##Bettinger T, Carlisle R C, Read M L, Ogris M, Seymour L W. Peptide-mediated RNA delivery: a novel approach for enhanced transfection of primary and post-mitotic cells. Nucleic acids research 2001; 29: 3882-3891.##Chang M-F, Hsieh J-H, Chiang H, Kan H-W, Huang C-M, Chellis L, et al. Effective gene expression in the rat dorsal root ganglia with a non-viral vector delivered via spinal nerve injection. Scientific Reports 2016; 6: 35612.##Connor B, Firmin E, McCaughey-Chapman A, Monk R, Lee K, Liot S, et al. Conversion of adult human fibroblasts into neural precursor cells using chemically modified mRNA. Heliyon 2018; 4: e00918.##Durymanov M, Reineke J. Non-viral Delivery of Nucleic Acids: Insight Into Mechanisms of Overcoming Intracellular Barriers. Frontiers in pharmacology 2018; 9: 971.##Erbacher P, Roche A C, Monsigny M, Midoux P. Putative role of chloroquine in gene transfer into a human hepatoma cell line by DNA/lactosylated polylysine complexes. Experimental cell research 1996; 225: 186-194.##Gómez-Aguado I, Rodríguez-Castejón J, Vicente-Pascual M, Rodríguez-Gascón A, Solinís M Á, Del Pozo-Rodríguez A. Nanomedicines to Deliver mRNA: State of the Art and Future Perspectives. Nanomaterials (Basel, Switzerland) 2020; 10: 364.##Hasan M T, Subbaroyan R, Chang T Y. High-efficiency stable gene transfection using chloroquine-treated Chinese hamster ovary cells. Somatic cell and molecular genetics 1991; 17: 513-517.##Holtkamp S, Kreiter S, Selmi A, Simon P, Koslowski M, Huber C, et al. Modification of antigen-encoding RNA increases stability, translational efficacy, and T-cell stimulatory capacity of dendritic cells. Blood 2006; 108: 4009-4017.##Homayouni F M, Sadeghi-Zadeh M, Alizadeh-Shoorjestan B, Dehghani-Varnamkhasti R, Narimani S, Darabi L, et al. Isolation and Culture of Embryonic Mouse Neural Stem Cells. Journal of visualized experiments: 2018 Nov 11;(141).##Joo K M, Jin J, Kang B G, Lee S J, Kim K H, Yang H, et al. Trans-differentiation of neural stem cells: a therapeutic mechanism against the radiation induced brain damage. PloS one 2012; 7: e25936.##Joshi C R, Labhasetwar V, Ghorpade A. Destination Brain: the Past, Present, and Future of Therapeutic Gene Delivery. J Neuroimmune Pharmacol 2017; 12: 51-83.##Kauffman K J, Mir F F, Jhunjhunwala S, Kaczmarek J C, Hurtado J E, Yang J H, et al. Efficacy and immunogenicity of unmodified and pseudouridine-modified mRNA delivered systemically with lipid nanoparticles in vivo. Biomaterials 2016; 109: 78-87.##Keravala A, Ormerod B K, Palmer T D, Calos M P. Long-term transgene expression in mouse neural progenitor cells modified with phiC31 integrase. Journal of neuroscience methods 2008; 173: 299-305.##Kužnik A, Benčina M, Švajger U, Jeras M, Rozman B, Jerala R. Mechanism of endosomal TLR inhibition by antimalarial drugs and imidazoquinolines. The Journal of Immunology 2011; 186: 4794-4804.##Lakshmipathy U, Pelacho B, Sudo K, Linehan J L, Coucouvanis E, Kaufman D S, et al. Efficient transfection of embryonic and adult stem cells. Stem Cells 2004; 22: 531-43.##Liang W, Lam J K. Endosomal escape pathways for non-viral nucleic acid delivery systems. Molecular regulation of endocytosis 2012: 429-456.##López-Lastra M, Rivas A, Barría M I. Protein synthesis in eukaryotes: the growing biological relevance of cap-independent translation initiation. Biological research 2005; 38: 121-146.##Mandal P K, Rossi D J. Reprogramming human fibroblasts to pluripotency using modified mRNA. Nature protocols 2013; 8: 568-582.##McLenachan S, Zhang D, Palomo A B A, Edel M J, Chen F K. mRNA transfection of mouse and human neural stem cell cultures. PLoS One 2013; 8: e83596.##Michel Y M, Poncet D, Piron M, Kean K M, Borman A M. Cap-poly (A) synergy in mammalian cell-free extracts investigation of the requirements for poly (a)-mediated stimulation of translation initiation. Journal of Biological Chemistry 2000; 275: 32268-32276.##Mockey M, Gonçalves C, Dupuy F P, Lemoine F M, Pichon C, Midoux P. mRNA transfection of dendritic cells: synergistic effect of ARCA mRNA capping with Poly (A) chains in cis and in trans for a high protein expression level. Biochemical and biophysical research communications 2006; 340: 1062-1068.##Ottoboni L, von Wunster B, Martino G. Therapeutic Plasticity of Neural Stem Cells. Frontiers in neurology 2020; 11: 148.##Patel S, Athirasala A, Menezes P P, Ashwanikumar N, Zou T, Sahay G, et al. Messenger RNA Delivery for Tissue Engineering and Regenerative Medicine Applications. Tissue engineering. Part A 2019; 25: 91-112.##PENG J, SCHOENBERG D R. mRNA with a&#60; 20-nt poly (A) tail imparted by the poly (A)-limiting element is translated as efficiently in vivo as long poly (A) mRNA. RNA 2005; 11: 1131-1140.##Pickard M R, Adams C F, Chari D M. Magnetic Nanoparticle-Mediated Gene Delivery to Two- and Three-Dimensional Neural Stem Cell Cultures: Magnet-Assisted Transfection and Multifection Approaches to Enhance Outcomes. Curr Protoc Stem Cell Biol 2017; 40: 2d.19.1-2d.19.16.##Preiss T. The end in sight: poly (A), translation and mRNA stability in eukaryotes. Translation Mechanisms 2002: 197-212.##Rietze R L, Reynolds B A. Neural stem cell isolation and characterization. Methods in enzymology. Vol 419: Elsevier, 2006: 3-23.##Rohani L, Fabian C, Holland H, Naaldijk Y, Dressel R, Löffler-Wirth H, et al. Generation of human induced pluripotent stem cells using non-synthetic mRNA. Stem cell research 2016; 16: 662-672.##Shih C-c, DiGiusto D, Mamelak A, LeBon T, Forman S J. Hematopoietic potential of neural stem cells: plasticity versus heterogeneity. Leukemia &#38; lymphoma 2002; 43: 2263-2268.##Wang Y, Su H-h, Yang Y, Hu Y, Zhang L, Blancafort P, et al. Systemic delivery of modified mRNA encoding herpes simplex virus 1 thymidine kinase for targeted cancer gene therapy. Molecular Therapy 2013; 21: 358-367.##Warren L, Lin C. mRNA-based genetic reprogramming. Molecular Therapy 2019; 27: 729-734.##Yakubov E, Rechavi G, Rozenblatt S, Givol D. Reprogramming of human fibroblasts to pluripotent stem cells using mRNA of four transcription factors. Biochemical and biophysical research communications 2010; 394: 189-193.##Zhang B, Mallapragada S. The mechanism of selective transfection mediated by pentablock copolymers; Part II: Nuclear entry and endosomal escape. Acta Biomaterialia 2011; 7: 1580-1587.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Which pharmaceutical agent is most commonly used for suicide? An epidemiological investigation inLoghman Hakim Hospital, 2018 - 2019</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Acute accidental and deliberate poisoning by medications and pharmaceuticals is the third cause of death in suicides after hanging and self-immolation. To determine the common pattern of intentional drug poisoning in Tehran, this descriptive and retrospective study has reviewed and analyzed the data related to the records of patients admitted due to intentional drug poisoning, 2018-2019 at Loghman-Hakim-Hospital-Poison-Center (LHHPC).
Methods: This is an epidemiological, cross-sectional investigation based on the medical profile of 9245 patients who were admitted to LHHPC for intentional drug poisoning from May 2018 to May 2019. The verified variables included: age, gender, type of drug used, previous history of mental health problems, presence or absence of a previous history of suicide, the outcome of hospitalization and time of emergency visit. All inquiry data were coded and statistically analyzed using SPSS Version 26 software.
Results: The average age of the admitted cases was 29.3&#177;12.4, with a minimum age of 12 years. The greatest proportion of poisoning occurred between the ages of 21-30 years. About 17.10% of patients had a previous history of self-harm and 57.77% had mental disorders. The most common pharmaceuticals for deliberate poisoning were anti-epileptics-sedative-hypnotics, antipyretics-non-opioid-analgesics, narcotics- hallucinogens and antidepressant-antipsychotic. Mortality was significantly higher in men and also following methadone and benzodiazepines.
Conclusion: The high prevalence of intentional poisoning and its resulting mortality among young adults requires considerable attention and further studies to understand the underlying causes. Besides, strict rules need to be enforced regarding the sale of central nervous system drugs and opioids.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>92</FPAGE>
			<TPAGE>99</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2020/10/262021/06/172021/08/272022/01/132021/08/172021/06/292021/11/112021/11/202021/08/152021/08/242021/10/9
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/7/17
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2022/01/52022/06/82021/12/42022/05/212022/05/302021/11/282022/04/112022/06/182022/04/302021/12/42022/06/20
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/3/30
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Masoumeh</Name>
				<MidName></MidName>
				<Family>Haji</Family>
				<NameE>Masoumeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Haji</FamilyE>
				<Organizations>
				<Organization>School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mitra</Name>
				<MidName></MidName>
				<Family>Rahimi</Family>
				<NameE>Mitra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rahimi</FamilyE>
				<Organizations>
				<Organization>Toxicological Research Center, Excellence Center of Clinical Toxicology, Department of Clinical Toxicology, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Khojasteh</Name>
				<MidName></MidName>
				<Family>Joharchi</Family>
				<NameE>Khojasteh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Joharchi</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>joharchi-kh@sbmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Intentional drug poisoning</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Medicines</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pharmaceuticals</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Suicide.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Ahmadi A, Pakravan N, Ghazizadeh Z. Pattern of acute food, drug, and chemical poisoning in Sari City, Northern Iran. Hum Exp Toxicol 2010; 29: 731-38. https://doi. org/10.1177/0960327110361501 ##Ajdacic-Gross V, Weiss MG, Ring M, Hepp U, Bopp M, Gutzwiller F, et al. Methods of suicide: international suicide patterns derived from the WHO mortality database. Bull World Health Organ 2008; 86: 726-32. https://doi. org/10.2471/BLT.07.043489 ##Ashrafioun L, Pigeon WR, Conner KR, Leong SH, Oslin DW. Prevalence and correlates of suicidal ideation and suicide attempts among veterans in primary care referred for a mental health evaluation. J Affect Disord 2016; 189: 344- 50. https://doi.org/10.1016/j.jad.2015.09.014 ##Bagge CL, Lee H-J, Schumacher JA, Gratz KL, Krull JL, Holloman JrG. Alcohol as an acute risk factor for recent suicide attempts: a case-crossover analysis. J Stud Alcohol Drugs 2013; 74: 552-8. https://doi.org/10.15288/jsad.2013.74.552 ##Borges G, Loera CR. Alcohol and drug use in suicidal behaviour. Curr Opin Psychiatry 2010; 23: 195-204. https:// doi.org/10.1097/YCO.0b013e3283386322 ##Callanan VJ, Davis MS. Gender differences in suicide methods. Soc Psychiatry Psychiatr Epidemiol 2012; 47: 857-69. https://doi.org/10.1007/s00127-011-0393-5 ##Chang B, Gitlin D, Patel R. The depressed patient and suicidal patient in the emergency department: evidence-based management and treatment strategies. Emerg Med Pract 2011; 13: 1-23. ##Eddleston M. Patterns and problems of deliberate self-poisoning in the developing world. Qjm 2000; 93: 715-31. https:// doi.org/10.1093/qjmed/93.11.715 ##Hassanian-Moghaddam H, Zamani N, Rahimi M, Shadnia S, Pajoumand A, Sarjami S. Acute adult and adolescent poisoning in Tehran, Iran; the epidemiologic trend between 2006 and 2011. Arch Iran Med 2014; 17: 534-8. ICD-10. ##International Classification of Diseases Version 10: Poisoning by, adverse effect of and underdosing of drugs, medicaments and biological substances T36-T50. Online ICD-10-CM Codes › S00-T88 2014. ##Karbakhsh M, Zandi NS. Pattern of poisoning in the elderly: an experience from Tehran. Clin Toxicol 2008; 46: 211- 217. https://doi.org/10.1080/15563650701638982 ##Kavak G, Aydin M, Altinbas K. Evaluation of suicide attempt by using medicines and chemicals. 2019. https://doi. org/10.26226/morressier.5b681762b56e9b005965c0db ##Kazemifar AM, Mirakbari SM, Yazdi Z, Bitazar B, Soleimani P. Clinicoepidemiologic profile of patients with poisoning presenting to a tertiary care hospital; a one year preliminary descriptive study. J prev epidemiol 2020; 5: 15. https://doi. org/10.34172/jpe.2020.15 ##Larney S, Topp L, Indig D, O’driscoll C, Greenberg D. A cross-sectional survey of prevalence and correlates of suicidal ideation and suicide attempts among prisoners in New South Wales, Australia. BMC public health 2012; 12: 1-7. https://doi.org/10.1186/1471-2458-12-14 ##Masoumi G, Eizadi-Mood N, Akabri M, Sohrabi A, Khalili Y. Pattern of poisoning in Isfahan. J Isfahan Med Sch 2012; 29. ##Moradi M, Ghaemi K, Mehrpour O. A hospital base epidemiology and pattern of acute adult poisoning across Iran: a systematic review. Electron Physician 2016; 8: 2860-70. https://doi.org/10.19082/2860 ##Moradinazar M, Najafi F, Baneshi MR, Haghdoost AA. Estimation of the rate and number of underreported deliberate self-poisoning attempts in western Iran in 2015. Epidemiol Health 2017; 39: e2017023. https://doi.org/10.4178/epih. e2017023 ##Murray CJ, Lopez AD. Evidence-based health policy--lessons from the Global Burden of Disease Study. Science 1996; 274: 740-3. https://doi.org/10.1126/science.274.5288.740 ##Pajoumand A. A one-year epidemiological study of acute poisoning among adults and adolescents admitted to Loghman hospital, Tehran between 2005 and 2006. Pajoohandeh J 2007; 12: 169-76. ##Pajoumand A, Talaie H, Mahdavinejad A, Birang S, Zarei M, Mehregan FF, et al. Suicide epidemiology and characteristics among young Iranians at poison ward, Loghman-Hakim Hospital (1997-2007). Arch Iran Med 2012; 15. ##Rezaeian M. Comparing the statistics of Iranian Ministry of Health with data of Iranian Statistical Center regarding recorded suicidal cases in Iran. HSR 2012.##Sarvestani RS. Sociology of Deviance: Social Pathology: SAMT 2019. ##Shadnia S, Esmaily H, Sasanian G, Pajoumand A, Hassanian-Moghaddam H, Abdollahi M. Pattern of acute poisoning in Tehran-Iran in 2003. Hum Exp Toxicol 2007; 26: 753- 756. https://doi.org/10.1177/0960327107083017 ##Shneidmann S. The suicidal mind. New York; Oxford University Publisher 1996. ##Sorodoc V, Jaba I M, Lionte C, Mungiu O C, Sorodoc L. Epidemiology of acute drug poisoning in a tertiary center from Iasi County, Romania. Hum Exp Toxicol 2011; 30: 1896- 903. https://doi.org/10.1177/0960327111403172 ##Spiller HA, Appana S, Brock GN. Epidemiological trends of suicide and attempted suicide by poisoning in the US: 2000- 2008. Leg Med 2010; 12: 177-83. https://doi.org/10.1016/j. legalmed.2010.04.005 ##Taghadosi Nejad F, Arefi M, Okazi A, Moradkhani A, Fayyaz A F. Neurological Sequels and Their Causes in Patients Hospitalized in the Toxicology Intensive Care Unit of Bahraloo Hospital, Tehran, Iran. J Arch Mil Med. 2015;3(2):e27950. https://doi.org/10.5812/jamm.3(2)2015.27950 ##WHO. Suicide in the world. Journal 2019: 32. https://doi. org/10.1016/S0262-1762(18)30421-8 ##Zakharov S, Navratil T, Pelclova D. Suicide attempts by deliberate self-poisoning in children and adolescents. Psychiatry Res 2013; 210: 302-7. https://doi.org/10.1016/j.psychres.2013.03.037## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>

</ARTICLES>

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