<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2022</YEAR>
<VOL>26</VOL>
<NO>4</NO>
<MOSALSAL>0</MOSALSAL>
<PAGE_NO>479</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>Pharmacological potential of ferulic acid for the treatment of metabolic syndrome and its mechanism of action: Review</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Recently, obesity causes vital mortality around the globe. Last decade, obesity-related diseases increased significantly worldwide. Even though, effective drugs are not available to treat metabolic diseases such as cardiovascular diseases, Parkinson&#8217;s, obesity, and hypertension. Emergence and identifying new drug moieties to treat such metabolic diseases became imperative. Nature is a vital source of remedies and isolates new effective and nontoxic drug candidates. Ferulic acid is a significant phenolic compound that is abundant in various fruits, rice oil, and vegetables. This study highlighted the beneficial effects of ferulic acid for the treatment of metabolic syndrome or obesity. Similarly, in this study, we have highlighted the therapeutic purpose of ferulic acid in treating metabolic syndrome, its mechanism of action as well as its potential pharmacological effect using animal models. Further investigations are needed to demonstrate the significant mechanism of action in clinical trials using the human species.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>345</FPAGE>
			<TPAGE>362</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/29
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/2/9
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/25
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/7/3
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Md. Reyad-ul</Name>
				<MidName></MidName>
				<Family>-Ferdous</Family>
				<NameE>Md. Reyad-ul</NameE>
				<MidNameE></MidNameE>
				<FamilyE>-Ferdous</FamilyE>
				<Organizations>
				<Organization>Department of Endocrinology and Metabolism, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China</Organization>
				</Organizations>
				<Countries>
				<Country>China</Country>
				</Countries>
				<EMAILS>
				<Email>rockyreyad@sdu.edu.cn</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Yongfeng</Name>
				<MidName></MidName>
				<Family>Song</Family>
				<NameE>Yongfeng</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Song</FamilyE>
				<Organizations>
				<Organization>Department of Endocrinology and Metabolism, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China</Organization>
				</Organizations>
				<Countries>
				<Country>China</Country>
				</Countries>
				<EMAILS>
				<Email>songyf@sdu.edu.cn</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Obesity and Metabolic diseases</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Lipid profiling and Glucose dysregulation</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cardioprotective</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antioxidant</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Inflammation and Hepatoprotective</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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Michelia alba extract attenuates UVB-induced expression of matrix metalloproteinases via MAP kinase pathway in human dermal fibroblasts. Food Chem Toxicol 2012; 50: 4260-9.##Cui L, Zhang Y, Cao H, Wang Y, Teng T, Ma G, et al. Ferulic acid inhibits the transition of amyloid-beta42 monomers to oligomers but accelerates the transition from oligomers to fibrils. J Alzheimers Dis 2013; 37: 19-28.##Das U, Manna K, Adhikary A, Mishra S, Saha K D, Sharma R D, et al. Ferulic acid enhances the radiation sensitivity of lung and liver carcinoma cells by collapsing redox homeostasis: mechanistic involvement of Akt/p38 MAPK signalling pathway. Free Radic Res 2019; 53: 944-967.##Das U, Manna K, Sinha M, Datta S, Das D K, Chakraborty A, et al. Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model. PLoS One 2014; 9: e97599.##de Melo T S, Lima P R, Carvalho K M, Fontenele T M, Solon F R, Tome A R, et al. 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Chem Pharm Bull (Tokyo) 1986; 34: 409-12.##Kelainy E G, Ibrahim Laila I M, Ibrahim S R. The effect of ferulic acid against lead-induced oxidative stress and DNA damage in kidney and testes of rats. Environ Sci Pollut Res Int 2019.##Kim E O, Min K J, Kwon T K, Um B H, Moreau R A, Choi S W. Anti-inflammatory activity of hydroxycinnamic acid derivatives isolated from corn bran in lipopolysaccharide-stimulated Raw 264.7 macrophages. Food Chem Toxicol 2012; 50: 1309-16.##Kim H S, Cho J Y, Kim D H, Yan J J, Lee H K, Suh H W, et al. Inhibitory effects of long-term administration of ferulic acid on microglial activation induced by intracerebroventricular injection of beta-amyloid peptide (1-42) in mice. Biol Pharm Bull 2004; 27: 120-1.##Kim J, Lee C W, Kim E K, Lee S J, Park N H, Kim H S, et al. Inhibition effect of Gynura procumbens extract on UV-B-induced matrix-metalloproteinase expression in human dermal fibroblasts. J Ethnopharmacol 2011; 137: 427-33.##Klop B, Elte J W, Cabezas M C. Dyslipidemia in obesity: mechanisms and potential targets. Nutrients 2013; 5: 1218-40.##Knauf C, Rieusset J, Foretz M, Cani P D, Uldry M, Hosokawa M, et al. Peroxisome proliferator-activated receptor-alpha-null mice have increased white adipose tissue glucose utilization, GLUT4, and fat mass: Role in liver and brain. Endocrinology 2006; 147: 4067-78.##Li T, Ferns K, Yan Z Q, Yin S Y, Kou J J, Li D, et al. Acanthopanax senticosus: Photochemistry and Anticancer Potential. American Journal of Chinese Medicine 2016; 44: 1543-1558.##Li X, Wang Y, Wang H, Huang C, Huang Y, Li J. Endoplasmic reticulum stress is the crossroads of autophagy, inflammation, and apoptosis signaling pathways and participates in liver fibrosis. Inflamm Res 2015; 64: 1-7.##Lim K H, Ko D, Kim J H. Cardioprotective potential of Korean Red Ginseng extract on isoproterenol-induced cardiac injury in rats. J Ginseng Res 2013; 37: 273-82.##Loos R J, Lindgren C M, Li S, Wheeler E, Zhao J H, Prokopenko I, et al. Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet 2008; 40: 768-75.##Mahmoud A M, Hussein O E, Abd El-Twab S M, Hozayen W G. Ferulic acid protects against methotrexate nephrotoxicity via activation of Nrf2/ARE/HO-1 signaling and PPARgamma, and suppression of NF-kappaB/NLRP3 inflammasome axis. Food Funct 2019; 10: 4593-4607.##Manach C, Scalbert A, Morand C, Remesy C, Jimenez L. Polyphenols: food sources and bioavailability. Am J Clin Nutr 2004; 79: 727-47.##Mancuso C, Santangelo R. Ferulic acid: pharmacological and toxicological aspects. Food Chem Toxicol 2014; 65: 185-95.##Mezzetti A, Cipollone F, Cuccurullo F. Oxidative stress and cardiovascular complications in diabetes: isoprostanes as new markers on an old paradigm. Cardiovasc Res 2000; 47: 475-88.##Mir S M, Ravuri H G, Pradhan R K, Narra S, Kumar J M, Kuncha M, et al. 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Biosci Trends 2016; 10: 386-391.##Okuda M, Fujita Y, Sugimoto H. The Additive Effects of Low Dose Intake of Ferulic Acid, Phosphatidylserine and Curcumin, Not Alone, Improve Cognitive Function in APPswe/PS1dE9 Transgenic Mice. Biol Pharm Bull 2019; 42: 1694-1706.##Ono K, Hirohata M, Yamada M. Ferulic acid destabilizes preformed beta-amyloid fibrils in vitro. Biochem Biophys Res Commun 2005; 336: 444-9.##Ou L, Kong L Y, Zhang X M, Niwa M. Oxidation of ferulic acid by Momordica charantia peroxidase and related anti-inflammation activity changes. Biol Pharm Bull 2003; 26: 1511-6.##Panchal S K, Brown L. Rodent models for metabolic syndrome research. J Biomed Biotechnol 2011; 2011: 351982.##Panchal S K, Poudyal H, Iyer A, Nazer R, Alam M A, Diwan V, et al. High-carbohydrate, high-fat diet-induced metabolic syndrome and cardiovascular remodeling in rats. J Cardiovasc Pharmacol 2011; 57: 611-24.##Park H J, Cho J H, Hong S H, Kim D H, Jung H Y, Kang I K, et al. 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Antidepressant‐Like Effect of Ferulic Acid via Promotion of Energy Metabolism Activity. Molecular Nutrition &#38; Food Research 2019; 63: 1900327.##Senaphan K, Kukongviriyapan U, Sangartit W, Pakdeechote P, Pannangpetch P, Prachaney P, et al. Ferulic Acid Alleviates Changes in a Rat Model of Metabolic Syndrome Induced by High-Carbohydrate, High-Fat Diet. Nutrients 2015; 7: 6446-64.##Seo J H, Chae Y C, Kossenkov A V, Lee Y G, Tang H Y, Agarwal E, et al. MFF Regulation of Mitochondrial Cell Death Is a Therapeutic Target in Cancer. Cancer Res 2019; 79: 6215-6226.##Sgarbossa A, Giacomazza D, di Carlo M. Ferulic Acid: A Hope for Alzheimer's Disease Therapy from Plants. Nutrients 2015; 7: 5764-82.##Sohn J W, Elmquist J K, Williams K W. Neuronal circuits that regulate feeding behavior and metabolism. Trends Neurosci 2013; 36: 504-12.##Sri Balasubashini M, Rukkumani R, Menon V P. Protective effects of ferulic acid on hyperlipidemic diabetic rats. Acta Diabetol 2003; 40: 118-22.##Srinivasan M, Sudheer A R, Menon V P. Ferulic Acid: therapeutic potential through its antioxidant property. J Clin Biochem Nutr 2007; 40: 92-100.##Sultana R, Ravagna A, Mohmmad-Abdul H, Calabrese V, Butterfield D A. Ferulic acid ethyl ester protects neurons against amyloid beta- peptide(1-42)-induced oxidative stress and neurotoxicity: relationship to antioxidant activity. J Neurochem 2005; 92: 749-58.##Suzuki A, Yamamoto M, Jokura H, Fujii A, Tokimitsu I, Hase T, et al. Ferulic acid restores endothelium-dependent vasodilation in aortas of spontaneously hypertensive rats. Am J Hypertens 2007; 20: 508-13.##Tailleux A, Wouters K, Staels B. Roles of PPARs in NAFLD: potential therapeutic targets. Biochim Biophys Acta 2012; 1821: 809-18.##Tsao R. Chemistry and biochemistry of dietary polyphenols. Nutrients 2010; 2: 1231-46.##Velloso L A, Araujo E P, de Souza C T. Diet-induced inflammation of the hypothalamus in obesity. 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Toxicol Lett 2013; 222: 72-82.##Yin C L, Lu R G, Zhu J F, Huang H M, Liu X, Li Q F, et al. The study of neuroprotective effect of ferulic acid based on cell metabolomics. Eur J Pharmacol 2019; 864: 172694.##Yuan J, Ge K, Mu J, Rong J, Zhang L, Wang B, et al. Ferulic acid attenuated acetaminophen-induced hepatotoxicity though down-regulating the cytochrome P 2E1 and inhibiting toll-like receptor 4 signaling-mediated inflammation in mice. Am J Transl Res 2016; 8: 4205-4214.##Zhao Z, Egashira Y, Sanada H. Ferulic acid sugar esters are recovered in rat plasma and urine mainly as the sulfoglucuronide of ferulic acid. J Nutr 2003; 133: 1355-61.##Zhao Z, Moghadasian M H. Chemistry, natural sources, dietary intake and pharmacokinetic properties of ferulic acid: A review. Food Chem 2008; 109: 691-702.##Zhou B, Kreuzer J, Kumsta C, Wu L, Kamer K J, Cedillo L, et al. Mitochondrial Permeability Uncouples Elevated Autophagy and Lifespan Extension. Cell 2019; 177: 299-314 e16.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Bioactive natural products against experimental autoimmune encephalomyelitis: A pharmacokinetics review</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Multiple sclerosis (MS) is a central nervous system (CNS) chronic disease in which axons are demyelinated and signal conduction is slowed or blocked. Unfortunately, current drugs that are used to treat MS have limited efficiency and considerable side effects. The use of bioactive natural products for treating neurodegenerative diseases has become of great interest due to their multimodal mechanism of action and potential safety. However, pharmacokinetic parameters such as bioavailability, absorption, metabolic pathways, and elimination routes are essential for evaluating the efficacy and toxicity of herbal medicines and herbal preparations in the clinic. In this review, we have summarized different pharmacokinetic parameters of neuroprotective natural products with anti-experimental autoimmune encephalomyelitis (EAE) effects and recent developments in strategies to improve their bioavailability and effectiveness.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>363</FPAGE>
			<TPAGE>394</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/30
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/11/11
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/31
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/6/9
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Leila</Name>
				<MidName></MidName>
				<Family>Mohtashami</Family>
				<NameE>Leila</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mohtashami</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacognosy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Abolfazl</Name>
				<MidName></MidName>
				<Family>Shakeri</Family>
				<NameE>Abolfazl</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shakeri</FamilyE>
				<Organizations>
				<Organization>Department of Pharmacognosy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Behjat</Name>
				<MidName></MidName>
				<Family>Javadi</Family>
				<NameE>Behjat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Javadi</FamilyE>
				<Organizations>
				<Organization>Department of Traditional Pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>javadib@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Multiple sclerosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Demyelination</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Natural products</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pharmacokinetics</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Experimental autoimmune encephalomyelitis</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Intraperitoneal Carbamylated erythropoietin improves memory and hippocampal apoptosis in beta-amyloid rat model of Alzheimer’s disease through stimulating autophagy and inhibiting necroptosis</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Alzheimer&#8217;s disease (AD) is marked by the deposition of amyloid-&#946; (A&#946;) plaques and tau tangles. Although Erythropoietin (EPO) provides neuroprotective and memory-improving properties, its application has been limited due to the hematopoietic effects. Carbamylated Erythropoietin-Fc (CEPO-Fc) was developed as a non-erythropoietic EPO derivative that possesses neuroprotective potential. However, the molecular mechanisms behind the protective effects of CEPO-Fc&#8217;s in AD are still under consideration. Therefore, herein investigated the therapeutic properties of intraperitoneal (i.p.) dose of CEPO-Fc on A&#946;-induced neurotoxicity in adult male Wistar rats. Methods: The rats received microinjections of A&#946;25-35 (5 &#956;g/2.5 &#956;l, per side) in the dorsal hippocampus for four consecutive days. CEPO-Fc was injected intraperitoneally in two doses of 500 and 5000 IU during the next six days. Learning and memory performance were studied (days 10-13) using the Morris Water Maze task. Immunoblotting was also undertaken to assess the molecular levels of leading indicators of apoptosis (Bax, Bcl-2, and caspase-3), necroptosis (Phosphorylated-Receptor-interacting serine/threonine-protein kinase 3 (p-RIP3)), as well as autophagy (phosphorylated-Beclin-1 (p-Beclin-1) and phosphorylated-1A/1B-light chain 3 (p-LC3-II)) in the hippocampus. Results: Behavioral analysis indicated that CEPO-Fc 500 and 5000 IU reversed memory impairment. Moreover, the hippocampus&#8217;s molecular study showed upregulation of P-LC3-II/LC3-II and suppression of Bax/Bcl-2, Caspase-3, and P-RIP3/RIP3 processes. Conclusion: Our findings imply that the neuroprotective characteristics of CEPO-Fc in the AD rats are mediated through autophagy activation and regulation of apoptosis and necroptosis processes. These results suggest that an i.p. dose of CEPO-Fc could be used to protect against AD-induced neurotoxicity.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>395</FPAGE>
			<TPAGE>411</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/2
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/4/11
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/7
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/5/16
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Amirhossein</Name>
				<MidName></MidName>
				<Family>Maghsoudi</Family>
				<NameE>Amirhossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Maghsoudi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Jalal</Name>
				<MidName></MidName>
				<Family>Zaringhalam</Family>
				<NameE>Jalal</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Zaringhalam</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Science, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>jzaringhalam@sbmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Moosavi</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Moosavi</FamilyE>
				<Organizations>
				<Organization>Nanomedicine and Nanobiology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Akram</Name>
				<MidName></MidName>
				<Family>Eidi</Family>
				<NameE>Akram</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Eidi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Apoptosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Autophagy</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Alzheimer’s disease</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Necroptosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Carbamylated Erythropoietin-Fc</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>The Impact of Crocin and Chronic Isolation Stress on Passive Avoidance Memory and Brain Electrical Activity in Male Rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Crocin and stress affect different aspects of brain functions. Chronic isolation stress is prevalent in today&#8217;s world. Therefore, this study investigated the impact of crocin and chronic isolation stress on learning, memory, and different brain waves in male rats. Methods: Forty male Wistar rats were allocated to five groups: control, sham, chronic isolation stress (CIS), two stress groups receiving different doses of crocin (CIS-Cr30 and CIS-Cr60). Both chronic isolation stress (6h/day) and crocin administration were induced for 21 days. The passive avoidance test evaluated initial and step-through latencies (IL and STL, respectively), as well as total dark compartment, and stay time. Also, different brain waves were measured by EEG recording. Results: The STL declined in the CIS and CIS-Cr30 groups while it significantly increased in only the CIS-Cr60 group. Also, the total dark compartment stay time increased in the CIS group, whereas it decreased by crocin (30 and 60 mg/kg) in the CIS group. The percentages of beta and alpha waves decreased whereas theta waves significantly increased in the CIS group. While the percentage of the beta and alpha waves increased as well as the percentage of the theta and delta waves decreased by crocin at a dose of 60 mg/kg in the CIS group. Conclusion: Cronic isolation stress was so destructive and it impaired learning, memory as well as alpha, beta, and theta waves in the brain. Only a dose of 60 mg/Kg of crocin reversed memory deficit and affected all brain waves in subjects under chronic isolation stress. Therefore, the doses of 60 and 30 mg/kg of crocin had different effects on electrophysiological and behavioral brain functions under chronic isolation conditions.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>412</FPAGE>
			<TPAGE>423</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/22
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/3/1
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/7
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/5/16
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>khani</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>khani</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Radahmadi</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Radahmadi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m_radahmadi@med.mui.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hojjatallah</Name>
				<MidName></MidName>
				<Family>Alaei</Family>
				<NameE>Hojjatallah</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alaei</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Isolation stress</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Crocin</KeyText>
			</KEYWORD>

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

			<KEYWORD>
				<KeyText>EEG</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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Effects of saffron (Crocus sativus L.) and its active constituent, crocin, on recognition and spatial memory after chronic cerebral hypoperfusion in rats. Phytotherapy Research 2012; 26: 381-386.##Hosseinzadeh H, Shamsaie F, Mehri S. Antioxidant activity of aqueous and ethanolic extracts of Crocus sativus L. stigma and its bioactive constituents, crocin and safranal. Pharmacognosy Magazine 2009; 5: 419.##Hosseinzadeh H, Shariaty V M, Sameni A K, Vahabzadeh M. Acute and sub-acute toxicity of crocin, a Constituent of crocus sativus L. (saffron), in Mice and Rats. Pharmacologyonline 2010 2 943-951##Hosseinzadeh H, Ziaei T. Effects of Crocus sativus stigma extract and its constituents, crocin and safranal, on intact memory and scopolamine-induced learning deficits in rats performing the Morris water maze task. Journal of Medicinal Plants 2006; 3: 40-50.##Jena S K. Examination stress and its effect on EEG. Int J Med Sci Pub Health 2015; 11: 1493-7.##Joëls M, Baram T Z. The neuro-symphony of stress. Nature reviews neuroscience 2009; 10: 459-466.##Kafa I M, Bakirci S, Uysal M, Kurt M A. Alterations in the brain electrical activity in a rat model of sepsis-associated encephalopathy. Brain Res 2010; 1354: 217-226.##Khalili M, Hamzeh F. Effects of active constituents of Crocus sativus L., crocin on streptozocin-induced model of sporadic Alzheimer's disease in male rats. Iranian biomedical journal 2010; 14: 59.##Khani F, Radahmadi M, Alaei H, Jafari E. Effects of crocin on cognitive and spatial memories in rats under chronic isolation stress. Physiology and Pharmacology 2018; 22: 254-268.##Khosravan V. Anticonvulsant effects of aqueous and ethanolic extracts of Crocus sativus L. stigmas in mice. Archives of Iranian Medicine 2002; 5: 44.##Kim J J, Diamond D M. The stressed hippocampus, synaptic plasticity and lost memories. Nature Reviews Neuroscience 2002; 3: 453.##Kirk I J, Spriggs M J, Sumner R L. Human EEG and the mechanisms of memory: investigating long-term potentiation (LTP) in sensory-evoked potentials. Journal of the Royal Society of New Zealand 2020: 1-17.##Knyazev G G, Savostyanov A N, Levin E A. Alpha synchronization and anxiety: implications for inhibition vs. alertness hypotheses. International Journal of Psychophysiology 2006; 59: 151-158.##Kumar J S, Bhuvaneswari P. Analysis of Electroencephalography (EEG) signals and its categorization-a study. Procedia engineering 2012; 38: 2525-2536.##Lagopoulos J, Xu J, Rasmussen I, Vik A, Malhi G S, Eliassen C F, et al. Increased theta and alpha EEG activity during nondirective meditation. The Journal of Alternative and Complementary Medicine 2009; 15: 1187-1192.##Loganathan S, Rathinasamy S. Alteration in memory and electroencephalogram waves with sub-acute noise stress in albino rats and safeguarded by scoparia dulcis. Pharmacognosy magazine 2016; 12: S7.##Lv B, Huo F, Zhu Z, Xu Z, Dang X, Chen T, et al. Crocin upregulates CX3CR1 expression by suppressing NF-κB/YY1 signaling and inhibiting lipopolysaccharide-induced microglial activation. Neurochemical research 2016; 41: 1949-1957.##Maoka T. Carotenoids as natural functional pigments. Journal of natural medicines 2020; 74: 1-16.##Masaki M, Aritake K, Tanaka H, Shoyama Y, Huang Z L, Urade Y. Crocin promotes non‐rapid eye movement sleep in mice. Molecular nutrition &#38; food research 2012; 56: 304-308.##McEwen B S. The ever‐changing brain: Cellular and molecular mechanisms for the effects of stressful experiences. Developmental neurobiology 2012; 72: 878-890.##McEwen B S, Gianaros P J. Stress-and allostasis-induced brain plasticity. Annual review of medicine 2011; 62: 431-445.##McEwen B S, Nasca C, Gray J D. Stress effects on neuronal structure: hippocampus, amygdala, and prefrontal cortex. Neuropsychopharmacology 2016; 41: 3-23.##McLaughlin K J, Gomez J L, Baran S E, Conrad C D. The effects of chronic stress on hippocampal morphology and function: an evaluation of chronic restraint paradigms. Brain research 2007; 1161: 56-64.##Miki Stein A, Munive V, Fernandez A M, Nuñez A, Torres Aleman I. Acute exercise does not modify brain activity and memory performance in APP/PS1 mice. PLoS One 2017; 12: e0178247.##Mrdalj J, Pallesen S, Milde A M, Jellestad F K, Murison R, Ursin R, et al. Early and later life stress alter brain activity and sleep in rats. PloS one 2013; 8: e69923.##Murao S, Yoto A, Yokogoshi H. Effect of smelling green tea on mental status and EEG activity. International Journal of Affective Engineering 2013; 12: 37-43.##Naghizadeh B, Mansouri M T, Ghorbanzadeh B, Farbood Y, Sarkaki A. Protective effects of oral crocin against intracerebroventricular streptozotocin-induced spatial memory deficit and oxidative stress in rats. Phytomedicine 2013; 20: 537-542.##Ndaro N Z, Wang S-Y. Effects of Fatigue Based on Electroencephalography Signal during Laparoscopic Surgical Simulation. Minimally invasive surgery 2018; 2018.##Papandreou M A, Tsachaki M, Efthimiopoulos S, Cordopatis P, Lamari F N, Margarity M. Memory enhancing effects of saffron in aged mice are correlated with antioxidant protection. Behavioural Brain Research 2011; 219: 197-204.##Paul C-M, Magda G, Abel S. Spatial memory: Theoretical basis and comparative review on experimental methods in rodents. Behavioural brain research 2009; 203: 151-164.##Pitsikas N, Sakellaridis N. Crocus sativus L. extracts antagonize memory impairments in different behavioural tasks in the rat. Behavioural brain research 2006; 173: 112-115.##Pitsikas N, Zisopoulou S, Tarantilis P A, Kanakis C D, Polissiou M G, Sakellaridis N. Effects of the active constituents of Crocus sativus L., crocins on recognition and spatial rats' memory. Behavioural Brain Research 2007; 183: 141-146.##Radahmadi M, Alaei H, Sharifi M R, Hosseini N. Preventive and therapeutic effect of treadmill running on chronic stress-induced memory deficit in rats. J Bodyw Mov Ther 2015; 19: 238-45.##Radahmadi M, Hosseini Dastgerdi A, Fallah N, Alaei H. The effects of acute, sub-chronic and chronic psychical stress on the brain electrical activity in male rats. Physiology and Pharmacology 2017; 21: 185-192.##Radahmadi M, Hosseini Dastgerdi A, Pourshanazari A A. Effects of crocin on locomotor activity as well as novel object recognition and object location memories in chronic restraint stressed rats. Physiology and Pharmacology 2020; 24: 123-132.##Rahimi S, Alaei H, Reisi P, Zarrin B, Siahmard Z, Pourshanazari A A. Hydroalcoholic tarooneh extract (Spathe of Phoenix Dactylifera) increased sedative-hypnotic effects and modulated electroencephalography brain waves in anesthetized rats. Advanced biomedical research 2019; 8.##Rajkishor P, Fumitoshi M, Bakardjia H, Vialatte F, Cichocki A. EEG changes after Bhramari Pranayama. Journal 2006: 390-395.##Ramesh V, Gozal D. Sleep fragmentation differentially modifies EEG delta power during slow wave sleep in socially isolated and paired mice. Sleep Science 2009; 2: 64-75.##Ranjbar H, Radahmadi M, Alaei H, Reisi P, Karimi S. The effect of basolateral amygdala nucleus lesion on memory under acute, mid and chronic stress in male rats. Turkish Journal of Medical Sciences 2016; 46: 1915-1925.##Roustazade R, Radahmadi M, Yazdani Y. Therapeutic effects of saffron extract on different memory types, anxiety, and hippocampal BDNF and TNF-α gene expressions in sub-chronically stressed rats. Nutritional Neuroscience 2021: 1-15.##Schacter D L. EEG theta waves and psychological phenomena: A review and analysis. Biological psychology 1977; 5: 47-82.##Schwabe L, Joëls M, Roozendaal B, Wolf O T, Oitzl M S. Stress effects on memory: an update and integration. Neuroscience &#38; Biobehavioral Reviews 2012; 36: 1740-1749.##Seo S-H, Lee J-T, Crisan M. Stress and EEG. Convergence and hybrid information technologies 2010; 1: 413-424.##Soeda S, Ochiai T, Shimeno H, Saito H, Abe K, Tanaka H, et al. Pharmacological activities of crocin in saffron. Journal of Natural Medicines 2007; 61: 102-111.##Sugiura M, Shoyama Y, Saito H, Abe K. Crocin (crocetin di-gentiobiose ester) prevents the inhibitory effect of ethanol on long-term potentiation in the dentate gyrus in vivo. Journal of Pharmacology and Experimental Therapeutics 1994; 271: 703-707.##Tamaddonfard E, Gooshchi N H, Seiednejad-Yamchi S. Central effect of crocin on penicillin-induced epileptiform activity in rats. Pharmacological Reports 2012; 64: 94-101.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>The effect of nanomicellar curcuminoids on renal ischemia/reperfusion injury and the expressions of COX-2 and Na+/K+-ATPase in rat’s kidney</TitleF>
		<TitleE> 
</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Renal Ischemia/Reperfusion (I/R) causes acute kidney injury known by impaired renal function, which has partially been connected to kidney apoptosis as well as the impairment of Cyclooxygenase-2 (COX-2) and Na+/K+-ATPase signaling. Curcuminoids have been proposed to have potential renoprotective effects. Thus, the present research work aimed to assess the effect of Nanomicellar Curcuminoids (NC) in a rat model of renal I/R. Methods: Adult male Sprague-Dawley rats were allocated to three treatment groups (n=5/ group). NC at the dose of 25 mg/kg/i.p or its vehicle was administered 60 min before renal ischemia induction. Then, the animals were subjected to bilateral renal ischemia for 60 min and reperfusion for 24 h. Subsequently, blood samples were collected to assess Blood Urea Nitrogen (BUN) and Creatinine (Cr) levels. In addition, kidneys were isolated to evaluate renal histopathology, caspase-3 cleavage, and COX-2 and Na+/K+ -ATPase pump levels. Results: The results showed that NC improved kidney function (P&#60;0.0001) and attenuated I/R-induced histopathological injuries (P&#60;0.0001) and caspase-3 cleavage (P&#60;0.01). However, the downregulation of renal COX-2 and Na+/K+ -ATPase expression induced by I/R was not restored by the renoprotective dose of NC. Conclusion: The findings of the present study indicated that the renoprotective effect of NC in the renal I/R rat model coincided with the inhibition of histopathological injuries and apoptosis, but not with compensation for renal COX-2 and Na+/K+ -ATPase downregulation.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>424</FPAGE>
			<TPAGE>432</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/26
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/11/7
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/28
		</ACCEPT_DATE>

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

		<AUTHORS>
			<AUTHOR>
				<Name>Zeinab</Name>
				<MidName></MidName>
				<Family>Karimi</Family>
				<NameE>Zeinab</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Karimi</FamilyE>
				<Organizations>
				<Organization>Shiraz Nephro-urology Research Center, Shiraz University of Medical sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Roksana</Name>
				<MidName></MidName>
				<Family>Soukhaklari</Family>
				<NameE>Roksana</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Soukhaklari</FamilyE>
				<Organizations>
				<Organization>Shiraz Neuroscience Research Center, Shiraz University of Medical sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Leila</Name>
				<MidName></MidName>
				<Family>Malekmakan</Family>
				<NameE>Leila</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Malekmakan</FamilyE>
				<Organizations>
				<Organization>Shiraz Nephro-urology Research Center, Shiraz University of Medical sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Zahra</Name>
				<MidName></MidName>
				<Family>Esmaili</Family>
				<NameE>Zahra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Esmaili</FamilyE>
				<Organizations>
				<Organization>Nanomedicine and Nanobiology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Moosavi</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Moosavi</FamilyE>
				<Organizations>
				<Organization>Nanomedicine and Nanobiology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>marmoosavi@sums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Curcuminoids</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Nanoparticle</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Renal ischemia/reperfusion</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Na+/K+ -ATPase</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>COX-2</KeyText>
			</KEYWORD>

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

		<REFRENCES>
			<REFRENCE>
				<REF>Amalraj A, Pius A, Gopi S, Gopi S. Biological activities of curcuminoids, other biomolecules from turmeric and their derivatives - A review. Journal of traditional and complementary medicine 2016; 7: 205-233.##Amiri E, Ghasemi R, Moosavi M. Agmatine Protects Against 6-OHDA-Induced Apoptosis, and ERK and Akt/GSK Disruption in SH-SY5Y Cells. Cellular and Molecular Neurobiology 2016; 36: 829-838.##Aydin M S, Caliskan A, Kocarslan A, Kocarslan S, Yildiz A, Günay S, et al. Intraperitoneal curcumin decreased lung, renal and heart injury in abdominal aorta ischemia/reperfusion model in rat. Int J Surg 2014; 12: 601-5.##Clausen M V, Hilbers F, Poulsen H. The Structure and Function of the Na,K-ATPase Isoforms in Health and Disease. Frontiers in physiology 2017; 8: 371-371.##Dawidczyk C M, Kim C, Park J H, Russell L M, Lee K H, Pomper M G, et al. State-of-the-art in design rules for drug delivery platforms: lessons learned from FDA-approved nanomedicines. Journal of Controlled Release 2014; 187: 133-144.##Feitoza C Q, Câmara N O, Pinheiro H S, Gonçalves G M, Cenedeze M A, Pacheco-Silva A, et al. Cyclooxygenase 1 and/or 2 blockade ameliorates the renal tissue damage triggered by ischemia and reperfusion injury. International immunopharmacology 2005; 5: 79-84.##Féraille E, Doucet A. Sodium-potassium-adenosinetriphosphatase-dependent sodium transport in the kidney: hormonal control. Physiological reviews 2001; 81: 345-418.##Gholampour F, Roozbeh J, Janfeshan S, Karimi Z. Remote ischemic per-conditioning protects against renal ischemia-reperfusion injury via suppressing gene expression of TLR4 and TNF-alpha in rat model. Can J Physiol Pharmacol 2019; 97: 112-119.##Goetz Moro M, Vargas Sánchez P K, Lupepsa A C, Baller E M, Nobre Franco G C. Cyclooxygenase biology in renal function - literature review. Revista Colombiana de Nefrología 2017; 4: 27-37.##Hatamipour M, Sahebkar A, Alavizadeh S H, Dorri M, Jaafari M R. Novel nanomicelle formulation to enhance bioavailability and stability of curcuminoids. Iran J Basic Med Sci 2019; 22: 282-289.##Hwang H S, Yang K J, Park K C, Choi H S, Kim S H, Hong S Y, et al. Pretreatment with paricalcitol attenuates inflammation in ischemia-reperfusion injury via the up-regulation of cyclooxygenase-2 and prostaglandin E2. Nephrology Dialysis Transplantation 2013; 28: 1156-1166.##Kar F, Hacioglu C, Senturk H, Donmez D B, Kanbak G, Uslu S. Curcumin and LOXblock-1 ameliorate ischemia-reperfusion induced inflammation and acute kidney injury by suppressing the semaphorin-plexin pathway. Life Sci 2020; 256: 118016.##Karahan M A, Yalcin S, Aydogan H, Büyükfirat E, Kücük A, Kocarslan S, et al. Curcumin and dexmedetomidine prevents oxidative stress and renal injury in hind limb ischemia/reperfusion injury in a rat model. Renal Failure 2016; 38: 693-698.##Karimi Z, SoukhakLari R, Rahimi-Jaberi K, Esmaili Z, Moosavi M. Nanomicellar curcuminoids attenuates renal ischemia/reperfusion injury in rat through prevention of apoptosis and downregulation of MAPKs pathways. Mol Biol Rep 2021; 48: 1735-1743.##Kaur A, Kaur T, Singh B, Pathak D, Singh Buttar H, Pal Singh A. Curcumin alleviates ischemia reperfusion-induced acute kidney injury through NMDA receptor antagonism in rats. Ren Fail 2016; 38: 1462-1467.##Liu F, Ni W, Zhang J, Wang G, Li F, Ren W. Administration of Curcumin Protects Kidney Tubules Against Renal Ischemia-Reperfusion Injury (RIRI) by Modulating Nitric Oxide (NO) Signaling Pathway. Cell Physiol Biochem 2017; 44: 401-411.##Liu F H, Ni W J, Wang G K, Zhang J J. Protective role of curcumin on renal ischemia reperfusion injury via attenuating the inflammatory mediators and Caspase-3. Cell Mol Biol (Noisy-le-grand) 2016a; 62: 95-99.##Liu W, Zhai Y, Heng X, Che F Y, Chen W, Sun D, et al. Oral bioavailability of curcumin: problems and advancements. Journal of drug targeting 2016b; 24: 694-702.##Lugo-Baruqui J A, Ayyathurai R, Sriram A, Pragatheeshwar K D. Use of Mannitol for Ischemia Reperfusion Injury in Kidney Transplant and Partial Nephrectomies-Review of Literature. Current Urology Reports 2019; 20: 6.##Malek M, Nematbakhsh M. Renal ischemia/reperfusion injury; from pathophysiology to treatment. Journal of renal injury prevention 2015; 4: 20-27.##Matsuzaki T, Watanabe H, Yoshitome K, Morisaki T, Hamada A, Nonoguchi H, et al. Downregulation of organic anion transporters in rat kidney under ischemia/reperfusion-induced acute [corrected] renal failure. Kidney Int 2007; 71: 539-47.##McComb S, Chan P K, Guinot A, Hartmannsdottir H, Jenni S, Dobay M P, et al. Efficient apoptosis requires feedback amplification of upstream apoptotic signals by effector caspase-3 or -7. Sci Adv 2019; 5: eaau9433.##Moosavi M, Abbasi L, Zarifkar A, Rastegar K. The role of nitric oxide in spatial memory stages, hippocampal ERK and CaMKII phosphorylation. Pharmacol Biochem Behav 2014; 122: 164-72.##Najafi H, Changizi Ashtiyani S, Sayedzadeh S A, Mohamadi Yarijani Z, Fakhri S. Therapeutic effects of curcumin on the functional disturbances and oxidative stress induced by renal ischemia/reperfusion in rats. Avicenna J Phytomed 2015; 5: 576-86.##Nørregaard R, Kwon T-H, Frøkiær J. Physiology and pathophysiology of cyclooxygenase-2 and prostaglandin E2 in the kidney. Kidney Research and Clinical Practice 2015; 34: 194-200.##Patel N S, Cuzzocrea S, Collino M, Chaterjee P K, Mazzon E, Britti D, et al. The role of cycloxygenase-2 in the rodent kidney following ischaemia/reperfusion injury in vivo. European journal of pharmacology 2007; 562: 148-154.##Prasad S, Tyagi A K, Aggarwal B B. Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: the golden pigment from golden spice. Cancer research and treatment : official journal of Korean Cancer Association 2014; 46: 2-18.##Sampaio L S, Iannotti F A, Veneziani L, Borelli-Tôrres R T, De Maio F, Piscitelli F, et al. Experimental ischemia/reperfusion model impairs endocannabinoid signaling and Na+/K+ ATPase expression and activity in kidney proximal tubule cells. Biochemical Pharmacology 2018; 154: 482-491.##Shiva N, Sharma N, Kulkarni Y A, Mulay S R, Gaikwad A B. Renal ischemia/reperfusion injury: An insight on in vitro and in vivo models. Life Sciences 2020: 117860.##Soares R O S, Losada D M, Jordani M C, Évora P, Castro-E-Silva O. Ischemia/Reperfusion Injury Revisited: An Overview of the Latest Pharmacological Strategies. International journal of molecular sciences 2019; 20: 5034.##Suleyman B, Albayrak A, Kurt N, Demirci E, Gundogdu C, Aksoy M. The effect of etoricoxib on kidney ischemia-reperfusion injury in rats: A biochemical and immunohistochemical assessment. International immunopharmacology 2014; 23: 179-185.##Suleyman Z, Sener E, Kurt N, Comez M, Yapanoglu T. The effect of nimesulide on oxidative damage inflicted by ischemia-reperfusion on the rat renal tissue. Renal failure 2015; 37: 323-331.##Villanueva S, Céspedes C, González A A, Vio C P, Velarde V. Effect of ischemic acute renal damage on the expression of COX-2 and oxidative stress-related elements in rat kidney. American Journal of Physiology-Renal Physiology 2007; 292: F1364-F1371.##Williams H D, Trevaskis N L, Charman S A, Shanker R M, Charman W N, Pouton C W, et al. Strategies to address low drug solubility in discovery and development. Pharmacol Rev 2013; 65: 315-499.##Wright J, Healy T, Balfour T, Hardcastle J. Effects of inhalation anaesthetic agents on the electrical and mechanical activity of the rat duodenum. British journal of anaesthesia 1982; 54: 1223-1230.##Xu Y, Hu N, Jiang W, Yuan H F, Zheng D H. Curcumin-carrying nanoparticles prevent ischemia-reperfusion injury in human renal cells. Oncotarget 2016; 7: 87390-87401.##Yang B, Lan S, Dieudé M, Sabo-Vatasescu J-P, Karakeussian-Rimbaud A, Turgeon J, et al. Caspase-3 Is a Pivotal Regulator of Microvascular Rarefaction and Renal Fibrosis after Ischemia-Reperfusion Injury. Journal of the American Society of Nephrology : JASN 2018; 29: 1900-1916.##Zhang J, Tang L, Li G S. The anti-inflammatory effects of curcumin on renal ischemia-reperfusion injury in rats. 2018; 40: 680-686.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>The methanolic extract of Zingiber officinale causes hypoglycemia and proinflammatory response in the rat pancreas</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Zingiber officinale (Ginger) is a commonly used plant for food and herbal treatment of different ailments. There is proof of ginger&#8217;s antioxidative and hypoglycemic activity, but the mechanism of action is yet to be understood, especially in a non-disease model. The present study assessed the effects of the methanolic extract of Zingiber officinale (MEZO) on blood glucose, pancreatic antioxidant levels, and histopathological changes. Methods: Fifteen (15) female Wistar rats with an average weight of 147 g were randomly divided into three (3) groups (A-C). Group A was given no treatment and served as the control group. Groups B and C received only oral administration of 400 mg/kg and 800mg/kg of MEZO, respectively. MEZO was administered once a day for 21 days. The animals were euthanized by cervical dislocation for blood collection and retrieval of pancreatic tissue for oxidative stress and histopathological assessment. Results: The serum glucose level was significantly decreased in group C compared to the control (P=0.012). There were no significant changes in the levels of Superoxide dismutase (SOD), Glutathione (GSH), and Catalase (CAT) in all the MEZO groups compared to
the control (P&#62;0.05). Pancreatic histology showed signs of acute pancreatitis, with dense aggregates of polymorphonuclear inflammatory cells infiltrating the surrounding stroma. Conclusion: A high-dose ginger extract induces hypoglycemia, but a proinflammatory response is elicited in the pancreas at a lower dose. Thus, ginger extracts should be consumed with caution.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>433</FPAGE>
			<TPAGE>439</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/262021/04/19
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/1/30
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/282021/09/25
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/7/3
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Izuchukwu Azuka</Name>
				<MidName></MidName>
				<Family>Okafor</Family>
				<NameE>Izuchukwu Azuka</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Okafor</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Faculty of Basic Medical Sciences, College of Health Sciences, Nnamdi Azikiwe University, Nnewi Campus, PMB 5001, Nnewi, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>iza.okafor@unizik.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Uchenna Somtochukwu</Name>
				<MidName></MidName>
				<Family>Okafor</Family>
				<NameE>Uchenna Somtochukwu</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Okafor</FamilyE>
				<Organizations>
				<Organization>Pan African University of Life and Earth Science Institute (Including Health and Agriculture), PAULESI, University of Ibadan, Ibadan, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>okaforu@babcock.edu.ng</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ginger</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pancreas</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Hypoglycemia</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antioxidants</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Inflammation</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abd El-Haleem, M. R., &#38; Mohamed, D. A. (2011). The effects of experimental aflatoxicosis on the pancreas of adult male albino rats and the role of ginger supplementation. The Egyptian Journal of Histology.##Abdulrazaq, N. B., Cho, M. M., Win, N. N., Zaman, R., &#38; Rahman, M. T. (2012). Beneficial effects of ginger (Zingiber officinale) on carbohydrate metabolism in streptozotocin-induced diabetic rats. British Journal of Nutrition.##Al-Qudah, M. M. A., Haddad, M. A., &#38; El-Qudah, J. M. F. (2016). The effects of aqueous ginger extract on pancreas histology and on blood glucose in normal and alloxan monohydrate-induced diabetic rats. Biomedical Research (India).##Arablou, T., Aryaeian, N., Valizadeh, M., Sharifi, F., Hosseini, A., &#38; Djalali, M. (2014). The effect of ginger consumption on glycemic status, lipid profile and some inflammatory markers in patients with type 2 diabetes mellitus. International Journal of Food Sciences and Nutrition.##Ataman, J. E., &#38; Ojukwu, F. (2014). Protective Effects of Aqueous Extract of Ginger on Castor-oil - Induced Testicular Damage in Wistar Rats. 14(4), 199–205.##Committee for the Update of the Guide for the Care and Use of Laboratory Animals, Institute for Laboratory Animal Research, Division on Earth and Life Studies, &#38; National Research Council. (2011). Guide for the care and use of laboratory animals (8th ed.). National Academies Press.##Guillen J. (2012). FELASA guidelines and recommendations. Journal of the American Association for Laboratory Animal Science : JAALAS, 51(3), 311–321.##Habib, S. H. M., Makpol, S., Hamid, N. A. A., Das, S., Ngah, W. Z. W., &#38; Yusof, Y. A. M. (2008). Ginger extract (Zingiber officinale) has anti-cancer and anti-inflammatory effects on ethionine-induced hepatoma rats. Clinics.##Hosseinzadeh, A., Bahrampour Juybari, K., Fatemi, M. J., Kamarul, T., Bagheri, A., Tekiyehmaroof, N., &#38; Sharifi, A. M. (2017). Protective Effect of Ginger (Zingiber officinale Roscoe) Extract against Oxidative Stress and Mitochondrial Apoptosis Induced by Interleukin-1β in Cultured Chondrocytes. Cells Tissues Organs.##Imani, A. M., &#38; Ainehchi, N. (2014). Comparison of the Effects of Methotrexate and Ginger Extract on Reproductive Parameters in Rats. 1(3), 103–109.##Jafarnejad, S., Keshavarz, S. A., Mahbubi, S., Saremi, S., Arab, A., Abbasi, S., &#38; Djafarian, K. (2017). Effect of ginger (Zingiber officinale) on blood glucose and lipid concentrations in diabetic and hyperlipidemic subjects: A meta-analysis of randomized controlled trials. In Journal of Functional Foods.##Jean-Marie, E. (2018). Diagnosis and classification of diabetes mellitus. In Encyclopedia of Endocrine Diseases.##Jolad, S. D., Lantz, R. C., Solyom, A. M., Chen, G. J., Bates, R. B., &#38; Timmermann, B. N. (2004). Fresh organically grown ginger (Zingiber officinale): Composition and effects on LPS-induced PGE2 production. Phytochemistry, 65(13), 1937–1954.##Khansari, N., Shakiba, Y., &#38; Mahmoudi, M. (2009). Chronic inflammation and oxidative stress as a major cause of age-related diseases and cancer . Chronic Inflammation and Oxidative Stress as a Major Cause of Age-Related Diseases and Cancer. June 2015.##Kilkenny, C., Browne, W., Cuthill, I. C., Emerson, M., Altman, D. G., &#38; NC3Rs Reporting Guidelines Working Group (2010). Animal research: reporting in vivo experiments: the ARRIVE guidelines. British journal of pharmacology, 160(7), 1577–1579.##Lantz, R. C., Chen, G. J., Sarihan, M., Sólyom, A. M., Jolad, S. D., &#38; Timmermann, B. N. (2007). The effect of extracts from ginger rhizome on inflammatory mediator production. Phytomedicine.##Mahluji, S., Attari, V. E., Mobasseri, M., Payahoo, L., Ostadrahimi, A., &#38; Golzari, S. E. (2013). Effects of ginger (Zingiber officinale) on plasma glucose level, HbA1c and insulin sensitivity in type 2 diabetic patients. International Journal of Food Sciences and Nutrition.##Mashhadi, N. S., Ghiasvand, R., Askari, G., Hariri, M., Darvishi, L., &#38; Mofid, M. R. (2013). Anti-oxidative and anti-inflammatory effects of ginger in health and physical activity: Review of current evidence. In International Journal of Preventive Medicine.##Mbaveng, A. T., &#38; Kuete, V. (2017). Zingiber officinale. In Medicinal Spices and Vegetables from Africa: Therapeutic Potential Against Metabolic, Inflammatory, Infectious and Systemic Diseases.##McGuckin, E., Cade, J. E., &#38; Hanison, J. (2020). The pancreas. In Anaesthesia and Intensive Care Medicine.##Minaiyan, A, G., &#38; A, K. (2006). Anti-ulcerogenic effect of ginger (rhizome of Zingiber officinale Roscoe) on cysteamine induced duodenal ulcer in rats. Daru.##Okafor, I. A., Ayalokunrin, M. B., &#38; Orachu, L. A. (2014). A review on Portulaca oleracea (Purslane) plant Its nature and biomedical benefits. International Journal of Biomedical Research, 5(2), 75–80.##Okafor, I. A., &#38; Gbotolorun, S. C. (2018). Resveratrol prevents cisplatin-induced lipid peroxidation in the non-gravid uterus of Sprague-Dawley rats. Middle East Fertility Society Journal.##Okafor, I. A., Nnamah, U. S., Nweke, J. O., Nnaka, J. A., Ahiatrogah S., &#38;  Okeke, U. V. (2020a). Zingiber officinale (Ginger) extract has no effect on Kiss1 gene expression in the testis and blood but may cause inflammation-induced morphological sperm disruptions in Wistar rats. Acta Scientific Medical Sciences Volume 4 Issue 12: 17-25. DOI:##Okafor, I. A., Nnamah, U. S., Nweke, J. O., Nnaka, J. A., Ahiatrogah S., Okeke, U. V., &#38; Okoro, C. C. (2020b). The Role of Zingiber officinale (Ginger) Extract in the Kiss1 Gene Expression in the Ovary and Blood of Wistar Rats. Acta Scientific Medical Sciences Volume 4 Issue 11: 89-96. DOI:##Shahrajaban, M. H., Sun, W., &#38; Cheng, Q. (2019). Pharmacological Uses and Health Benefits of Ginger (Zingiber officinale) in Traditional Asian and Ancient Chinese Medicine, and Modern Practice. Notulae Scientia Biologicae.##Sharma, A., Flores-Vallejo, R. del C., Cardoso-Taketa, A., &#38; Villarreal, M. L. (2017). Antibacterial activities of medicinal plants used in Mexican traditional medicine. In Journal of Ethnopharmacology.##Shukla, Y., &#38; Singh, M. (2007). Cancer preventive properties of ginger: A brief review. In Food and Chemical Toxicology.##Tripathi, P., Gupta, G., &#38; Chauhan, P. S. (2018). Role of Phytomedicine in Diabetes and Cardiovascular Diseases. In New Look to Phytomedicine: Advancements in Herbal Products as Novel Drug Leads.##Yeh, H. yu, Chuang, C. hung, Chen, H. Chun, Wan, C. Jen, Chen, T. Liang, &#38; Lin, L. Yun. (2014). Bioactive components analysis of two various gingers (Zingiber officinale Roscoe) and antioxidant effect of ginger extracts. LWT - Food Science and Technology.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Ascorbic acid inhibits the acquisition and expression of morphine-induced conditioned place preference and sensitization in male Swiss-Webster mice</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Ascorbic acid is shown to reduce the signs of opioid dependence and addiction. The present experiments investigated the possible influence of ascorbic acid in acquiring and expressing morphine conditioned place preference (CPP) and sensitization in mice. Methods: Male Swiss-Webster mice (20-25 g) were used. The unbiased method and an open field procedure were conducted for place preference and sensitization studies, respectively. Animals received different doses of morphine (1, 5, 10, and 20 mg/kg), ascorbic acid (1, 10, 100, and 1000 mg/kg), or saline (10 ml/kg) for place preference studies. Ascorbic acid was injected into the animals 20 min before each morphine (5 mg/kg) injection (acquisition) or 20 min before the test of morphine CPP (expression). Mice received morphine (5 mg/ kg) for three consecutive days, followed by five resting days for sensitization. Animals&#8217; hyperactivity after morphine (1 mg/kg) challenge dose confirmed the sensitization. Ascorbic acid was administered 20 min before each morphine (5 mg/kg) injection (acquisition) or 20 min before each morphine challenge dose (1 mg/kg) administration on the test day (expression). Results: Morphine induced significant place preference dose-dependently. Furthermore, intraperitoneal (i.p.) administration of ascorbic acid failed to induce any aversion or preference effects. Ascorbic acid reduced the expression and acquisition of morphine place conditioning. Intraperitoneal injections of ascorbic acid also reduced the expression and acquisition of morphine sensitization. Conclusion: Ascorbic acid could affect the motivational effects of morphine in mice. The exact mechanism by which the vitamin reduces the morphine effect must be evaluated in future studies.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>440</FPAGE>
			<TPAGE>450</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/262021/04/192021/02/2
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/11/14
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/282021/09/252021/09/6
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/6/15
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Mohammad</Name>
				<MidName></MidName>
				<Family>Sahraei</Family>
				<NameE>Mohammad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sahraei</FamilyE>
				<Organizations>
				<Organization>Student Research Committee, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ali</Name>
				<MidName></MidName>
				<Family>Nasiri</Family>
				<NameE>Ali</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nasiri</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Leila</Name>
				<MidName></MidName>
				<Family>Hossein-Mardi</Family>
				<NameE>Leila</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hossein-Mardi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Islamic Azad University, Damghan Branch, Damghan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Nasrin</Name>
				<MidName></MidName>
				<Family>Faraji</Family>
				<NameE>Nasrin</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Faraji</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Islamic Azad University, Damghan Branch, Damghan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hedayat</Name>
				<MidName></MidName>
				<Family>Sahraei</Family>
				<NameE>Hedayat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sahraei</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>h.sahraei@bmsu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ascorbic Acid</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Conditioned place preference</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Morphine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Sensitization</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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The effect of microinjection of CART 55-102 into the nucleus accumbens shell on morphine-induced conditioned place preference in rats: Involvement of the NMDA receptor. Peptides 2020; 129: 170319.##Becker J A, Pellissier L P, Corde Y, Laboute T, Léauté A, Gandía J, et al. Facilitating mGluR4 activity reverses the long-term deleterious consequences of chronic morphine exposure in male mice. Neuropsychopharmacology 2020: 1-13.##Cammack J, Ghasemzadeh B, Adams R. The pharmacological profile of glutamate-evoked ascorbic acid efflux measured by in vivo electrochemistry. Brain research 1991; 565: 17-22.##Carlezon W A, Boundy V A, Haile C N, Lane S B, Kalb R G, Neve R L, et al. sensitization to morphine induced by viral-mediated gene transfer. Science 1997; 277: 812-815.##Carr A C, McCall C. The role of vitamin C in the treatment of pain: new insights. Journal of translational medicine 2017; 15: 77.##Charmchi E, Faramarzi G, Rashvand M, Zendehdel M, Haghparast A. Restraint Stress Potentiated Morphine Sensitization: Involvement of Dopamine Receptors within the Nucleus Accumbens. Neurochemical Research 2021 Mar;46(3):648-659. doi: 10.1007/s11064-020-03199-5. ##De Angelis L. Ascorbic acid and atypical antipsychotic drugs: modulation of amineptine-induced behavior in mice. Brain research 1995; 670: 303-307.##Deshpande C, Dhir A, Kulkarni S. Antagonistic activity of ascorbic acid (Vitamin C) on dopaminergic modulation: Apomorphine-induced stereotypic behavior in mice. Pharmacology 2006; 77: 38-45.##Di Chiara G, Imperato A. Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. Proceedings of the National Academy of Sciences 1988; 85: 5274-5278.##Diliberto Jr E J, Daniels A J, Viveros O H. Multicompartmental secretion of ascorbate and its dual role in dopamine β-hydroxylation. The American journal of clinical nutrition 1991; 54: 1163S-1172S.##Domjan M. 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European journal of pharmacology 1989; 172: 413-416.##Grünewald R. Ascorbic acid in the brain. Brain Research Reviews 1993; 18: 123-133.##Hnasko T S, Sotak B N, Palmiter R D. Morphine reward in dopamine-deficient mice. Nature 2005; 438: 854-857.##Johnson S, North R. Opioids excite dopamine neurons by hyperpolarization of local interneurons. Journal of neuroscience 1992; 12: 483-488.##Johnston P, Chahl L A. Chronic treatment with ascorbic acid inhibits the morphine withdrawal response in guinea-pigs. Neuroscience letters 1992; 135: 23-27.##Kalivas P, Duffy P. Sensitization to repeated morphine injection in the rat: possible involvement of A10 dopamine neurons. Journal of Pharmacology Experimental Therapeutics 1987; 241: 204-212.##Katsidoni V, Tzatzarakis M N, Karzi V, Thermos K, Kastellakis A, Panagis G. Differential effects of chronic voluntary wheel-running on morphine induced brain stimulation reward, motor activity and striatal dopaminergic activity. Behavioural Brain Research 2020; 394: 112831.##Khaksari M, Nakhaei P, Khastar H, Bakhtazad A, Rahimi K, Garmabi B. Circadian fluctuation in curiosity is a risk factor for morphine preference. Biological Rhythm Research 2020: 1-13.##Kimura K, Sidhu A. Ascorbic Acid Inhibits 125I‐SCH 23982 Binding but Increases the Affinity of Dopamine for D1 Dopamine Receptors. Journal of neurochemistry 1994; 63: 2093-2098.##Liang J, Ma S-S, Li Y-J, Ping X-J, Hu L, Cui C-L. Dynamic changes of tyrosine hydroxylase and dopamine concentrations in the ventral tegmental area-nucleus accumbens projection during the expression of morphine-induced conditioned place preference in rats. Neurochemical research 2012; 37: 1482-1489.##Liu J-l, Li S-q, Zhu F, Zhang Y-x, Wu Y-n, Yang J-s, et al. Tyrosine Hydroxylase Gene Polymorphisms Contribute to Opioid Dependence and Addiction by Affecting Promoter Region Function. NeuroMolecular Medicine 2020: 1-10.##Ma Y-Y, Meng L, Guo C-Y, Han J-S, Lee D Y-W, Cui C-L. Dose-and time-dependent, context-induced elevation of dopamine and its metabolites in the nucleus accumbens of morphine-induced CPP rats. Behavioural brain research 2009; 204: 192-199.##May J M, Qu Z-c, Meredith M E. Mechanisms of ascorbic acid stimulation of norepinephrine synthesis in neuronal cells. Biochemical biophysical research communications 2012; 426: 148-152.##Meredith M E, May J M. Regulation of embryonic neurotransmitter and tyrosine hydroxylase protein levels by ascorbic acid. Brain research 2013; 1539: 7-14.##Motahari A A, Sahraei H, Meftahi G H. Role of nitric oxide on dopamine release and morphine-dependency. Basic clinical neuroscience 2016; 7: 283.##Nejati S, Khakpai F, Zarrindast M-R. Synergistic effect between citalopram and citicoline on anxiolytic effect in non-sensitized and morphine-sensitized mice: an isobologram analysis. Brain research 2020; 1734: 146701.##Oke A F, May L, Adams R N. Ascorbic Acid Distribution Patterns in Human Brain: A Comparison with Nonhuman Mammalian Species a. Annals of the New York Academy of Sciences 1987; 498: 1-12.##Olmstead M C, Franklin K B. The development of a conditioned place preference to morphine: effects of microinjections into various CNS sites. Behavioral neuroscience 1997; 111: 1324.##Pinkerton E, Good P, Gibbons K, Hardy J. An open-label pilot study of oral vitamin C as an opioid-sparing agent in patients with chronic pain secondary to cancer. Supportive Care in Cancer 2017; 25: 341-343.##Pontieri F, Tanda G, Di Chiara G. Intravenous cocaine, morphine, and amphetamine preferentially increase extracellular dopamine in the&#34; shell&#34; as compared with the&#34; core&#34; of the rat nucleus accumbens. Proceedings of the National Academy of Sciences 1995; 92: 12304-12308.##Rebec G V, Pierce R C. A vitamin as neuromodulator: ascorbate release into the extracellular fluid of the brain regulates dopaminergic and glutamatergic transmission. Progress in neurobiology 1994; 43: 537-565.##Rebec G V, Wang Z. Behavioral activation in rats requires endogenous ascorbate release in striatum. Journal of Neuroscience 2001; 21: 668-675.##Rescorla R A. Behavioral studies of Pavlovian conditioning. Annual review of neuroscience 1988; 11: 329-352.##Sahraei H, Aliabadi A A, Zarrindast M-R, Ghoshooni H, Nasiri A, Barzegari-Sorkheh A A, et al. Ascorbic acid antagonizes nicotine-induced place preference and behavioral sensitization in mice. European journal of pharmacology 2007a; 560: 42-48.##Sahraei H, Barzegari A-A, Shams J, Zarrindast M-R, Haeri-Rohani A, Ghoshooni H, et al. Theophylline inhibits tolerance and sensitization induced by morphine: a conditioned place preference paradigm study in female mice. 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Neuropharmacology 2020; 176: 108217.##Zachry J E, Nolan S O, Brady L J, Kelly S J, Siciliano C A, Calipari E. Sex differences in dopamine release regulation in the striatum. Neuropsychopharmacology 2020: 1-9.##Zarrindast M-R, Gholami A, Sahraei H, Haeri-Rohani A. Role of nitric oxide in the acquisition and expression of apomorphine-or morphine-induced locomotor sensitization. European journal of pharmacology 2003; 482: 205-213.##Zelfand E. Vitamin C, Pain and Opioid Use Disorder. Integrative Medicine: A Clinician's Journal 2020; 19.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Fullerene C60 nanoparticle attenuates pain and tumor necrosis factor-α protein expression in the hippocampus following diabetic neuropathy in rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Diabetic neuropathy is a common complication of diabetes mellitus. It is associated with nerve damage due to oxidative stress and high levels of pro-inflammatory mediators. In the present study, we examined the anti-nociceptive effects of Fullerene nanoparticle, as a potent anti-oxidant, during diabetic neuropathy. Methods: Diabetes mellitus induced through injection of streptozotocin (STZ) (40 mg/kg). Four groups were used in the study as follows: the control, control+fullerene, diabetes, and diabetes +fullerene groups. All four groups received sesame oil. Treatment rats received fullerene C60 (1mg/kg/day) for 9 weeks by intra-gastric gavage. Then, cold allodynia, histology, and tumor necrosis factor-&#945; (TNF- &#945;) protein expression of the hippocampus were measured 9 weeks after injection of STZ. Results: Our data revealed that STZ induces cold allodynia in both hind paws and increases the TNF- &#945; protein expression in the hippocampus. Furthermore, STZ induces neural degeneration in the hippocampus. Additionally, fullerene C60 significantly attenuated cold allodynia and TNF- &#945; protein expression. Also, fullerene C60 has neuro-protective effects on hippocampal neurons. However, fullerene C60 did not significantly reduce serum glucose levels in diabetic animals. Conclusion: Our data suggest that fullerene C60 likely suppressed pain, and neural loss by inhibitory effects on TNF- &#945; protein expression in the hippocampus during diabetes.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>451</FPAGE>
			<TPAGE>458</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/262021/04/192021/02/22021/02/7
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/11/19
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/282021/09/252021/09/62021/08/31
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/6/9
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Fariba</Name>
				<MidName></MidName>
				<Family>Namdar</Family>
				<NameE>Fariba</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Namdar</FamilyE>
				<Organizations>
				<Organization>Pediatric Urology and Regenerative Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farideh</Name>
				<MidName></MidName>
				<Family>Bahrami</Family>
				<NameE>Farideh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bahrami</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Zahra</Name>
				<MidName></MidName>
				<Family>Bahari</Family>
				<NameE>Zahra</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bahari</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Bahram</Name>
				<MidName></MidName>
				<Family>Ghanbari</Family>
				<NameE>Bahram</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghanbari</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, Sharif University of Technology, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shima</Name>
				<MidName></MidName>
				<Family>Shahyad</Family>
				<NameE>Shima</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shahyad</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Taghi</Name>
				<MidName></MidName>
				<Family>Mohammadi</Family>
				<NameE>Mohammad Taghi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mohammadi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mohammadimohammadt@bmsu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Fullerene C60</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Diabetic Neuropathy</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>TNF-α</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Hippocampus</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Askary-Ashtiani A, Ghanjal A, Motaqi M, Meftahi GH, Hatef B, Niknam H. The isokinetic and electromyographic assessment of knee muscles strength in the short- and long-term type 2 diabetes. Asian J Sports Med. 2016; 7: 37008.##Bahari Z, Manaheji H, Hosseinmardi N, Meftahi GH, Sadeghi M, Danialy S, et al. Induction of spinal long-term synaptic potentiation is sensitive to inhibition of neuronal NOS in L5 spinal nerve-transected rats. EXCLI J. 2014; 13: 751-60.##Bayatpoor ME, Mirzaee S, Karami Abd M, Mohammadi MT, Shahyad S, Bahari Z, et al. Crocin treatment decreased pancreatic atrophy, LOX-1 and RAGE mRNA expression of pancreas tissue in cholesterol-fed and streptozotocin-induced diabetic rats. J Complement Integr Med. 2019; 20190117.##Callaghan BC, Cheng HT, Stables CL, Smith AL, Feldman EL. Diabetic neuropathy: clinical manifestations and current treatments. Lancet Neurol. 2012; 11: 521-34.##Choi Y, Yoon YW, Na HS, Kim SH, Chung JM. Behavioural signs of ongoing pain, cold allodynia in a rat model of neuropathic pain. Pain. 1994; 59: 369-76.##Covey WC, Ignatowski TA, Knight PR, Spengler RN. Brain-derived TNFα: involvement in neuroplastic changes implicated in the conscious perception of persistent pain. Brain Res. 2000; 859: 113-22.##del Rey A, Yau HJ, Randolf A, Centeno MV, Wildmann J, Martina M, et al. Chronic neuropathic pain-like behavior correlates with IL-1b expression and disrupts cytokine interactions in the hippocampus. Pain. 2011; 152:2827-35.##Debnath M, Agrawal S. Diabetic neuropathy: oxidative and neuroinflammation. EJPMR. 2016; 3: 237-41.##Duarte JMN. Metabolic alterations associated to brain dysfunction in diabetes. Aging Dis. 2015; 6: 304-21.##Farshid AA, Tamaddonfard E. Histopathological and behavioral evaluations of the effects of crocin, safranal and insulin on diabetic peripheral neuropathy in rats. Avicenna J Phytomed. 2015; 5: 469-78.##Feldman EL, Nave KA, Jensen TS, Bennett DLH. New horizons in diabetic neuropathy: mechanisms, bioenergetics, and pain. Neuron. 2017; 93: 1296-1313.##Fischer R, Maier O. Interrelation of oxidative stress and inflammation in neurodegenerative disease: role of TNF. Oxid Med Cell Longev. 2015; 2015: 610813.##Hadipour M, Bahari Z, Afarinesh MR, Jangravi Z, Shirvani H, Meftahi GH. Administering crocin ameliorates anxiety‐like behaviors and reduces the inflammatory response in amyloid‐beta induced neurotoxicity in rat. Clin Exp Pharmacol Physiol. 2021.##Husseini Y, Sahraei H, Meftahi GH, Dargahian M, Mohammadi A, Hatef B, et al. Analgesic and anti-inflammatory activities of hydro-alcoholic extract of Lavandula officinalis in mice: possible involvement of the cyclooxygenase type 1 and 2 enzymes. Revista Brasileira de Farmacognosia. 2016; 26: 102-8.##Ignatowski TA, Covey WC, Knight PR, Severin CM, Nickola TJ, Spengler RN. Brain-derived TNFα mediates neuropathic pain. Brain Res. 1999; 841: 70-7.##Ignatowski TA, Spengler RN. Targeting tumor necrosis factor in the brain relieves neuropathic pain. World J Anesthesiol. 2018; 7: 10-9.##Ismail CAN, Abd Aziz CB, Suppian R, Long I. Imbalanced oxidative stress and pro-inflammatory markers differentiate the development of diabetic neuropathy variants in streptozotocin-induced diabetic rats. J Diabetes Metab Disord. 2018; 17: 129-36.##Kuhad A, Chopra K. Tocotrienol attenuates oxidative-nitrosative stress and inflammatory cascade in experimental model of diabetic neuropathy. Neuropharmacology. 2009; 57: 456-62.##Liu MG, Chen J. Roles of the hippocampal formation in pain information processing. Neurosci Bull. 2009; 25: 237-66.##Liu Y, Zhou LJ, Wang X, Li D, Ren WJ, Peng J, Peng G, et al. TNF-α differentially regulates synaptic plasticity in the hippocampus and spinal cord by microglia-dependent mechanisms after peripheral nerve injury. J Neurosci. 2017; 37: 871-81.##Ling Q, Liu M, Wu MX, Xu Y, Yang J, Huang HH, et al. Anti-allodynic and neuroprotective effects of koumine, a benth alkaloid, in a rat model of diabetic neuropathy. Biol Pharm Bull. 2014; 37: 858-64.##Mangaiarkkarasi A, Rameshkannan S, Meher Ali R. Effect of gabapentin and pregabalin in rat model of taxol induced neuropathic pain. JCDR. 2015; 9: 11-14.##Mohd Shafri MA, Mat Jais AM, Mohamed F. Cresyl violet staining to assess neuroprotective and neuroregenerative effects of haruan traditional extract against neurodegenerative damage of ketamine. Int J Pharm Pharm Sci. 2012; 4: 163-8.##Negi G, Kumar A, Sharma SS. Melatonin modulates neuroinflammation and oxidative stress in experimental diabetic neuropathy: effects on NF‐κB and Nrf2 cascades. J Pineal Res. 2011; 50: 124-31.##Oyenihi AB, Ayeleso AO, Mukwevho E, Masola B. Antioxidant strategies in the management of diabetic neuropathy. Biomed Res Int. 2015; 2015: 515042.##Rasouli Vani J, Mohammadi MT, Sarami Foroshani M, Jafari M. Polyhydroxylated fullerene nanoparticles attenuate brain infarction and oxidative stress in rat model of ischemic stroke. EXCLI J. 2016; 15: 378-90.##Romero-Grimaldi C, Berrocoso E, Alba-Delgado C, Madrigal GLM, Perez-Nievas BG, Leza JC, et al. Stress increases the negative effects of chronic pain on hippocampal neurogenesis. Anesth Analg. 2015; 121: 1078-88.##Satoh J, Yagihashi S, Toyota T. The possible role of tumor necrosis factor-α in diabetic polyneuropathy. Experimental Diab Res. 2003; 4: 65-71.##Sandireddy R, Yerra VG, Areti A, Komirishetty P, Kumar A. Neuroinflammation and oxidative stress in diabetic neuropathy: futuristic strategies based on these targets. Int J Endocrinol. 2014; 2014: 674987.##Sarami Foroshani M, Mohammadi MT. Functionalized fullerene materials (fullerol nanoparticles) reduce brain injuries during cerebral ischemia-reperfusion in rat. JPHS. 2016; 4: 15-21.##Schleicher E, Friess U. Oxidative stress, AGE, and atherosclerosis. Kidney Int. 2007; 106: 17-26.##Schreiber AK, Nones CFM, Reis RC, Chichorro JG, Cunha JM. Diabetic neuropathic pain: physiopathology and treatment. World J Diabetes. 2015; 6: 432-44.##Sha J, Sui B, Su X, Meng Q, Zhang C. Alteration of oxidative stress and inflammatory cytokines induces apoptosis in diabetic nephropathy. Mol Med Rep. 2017; 16: 7715-23.##Solleiro-Villavicencio H, Rivas-Arancibia S. Effect of chronic oxidative stress on neuroinflammatory response mediated by CD4+T cells in neurodegenerative diseases. Front Cell Neurosci. 2018; 12: 114.##Xu GY, Li G, Liu N, Mae Huang LY. Mechanisms underlying purinergic P2X3 receptormediated mechanical allodynia induced in diabetic rats. Mol Pain. 2011; 7: 60.##Yang E, Gavini K, Bhakta A, Dhanasekaran M, Khan I, Parameshwaran K. Streptozotocin induced hyperglycemia stimulates molecular signaling that promotes cell cycle reentry in mouse hippocampus. Life Sci. 2018; 205: 131-5.##Zhu GC, Tsai KL, Chen YW, Hung CH. Neural mobilization attenuates mechanical allodynia and decreases proinflammatory cytokine concentrations in rats with painful diabetic neuropathy. Phys Ther. 2018; 98: 214-22.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of prenatal consumption of Combretum dolichopetalum by pregnant rats on haematological and biochemical parameters as well as pregnancy outcome</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Combretum dolichopetalum (CD) is commonly found in the Eastern part of Nigeria where it is used to relieve menstrual pain, enhance labour, facilitate the removal of placenta and promote a rich milk supply after delivery. This study investigates the effect of prenatal consumption of Combretum dolichopetalum by pregnant albino rats on haematological, and biochemical parameters as well as pregnancy outcome. Methods: Mature inbred healthy female albino rats of normal estrus cycles that were 2-3 months of age weighting 120-180 g were used for the study. Examination of the estrus cycle, the introduction of male rats at pro-estrus, and confirmation of pregnancy were adopted using standard method. After initiation of pregnancy, fifty (50) rats were placed in five groups comprising ten rats per group. Distilled water was administered to rats in Group 1 which served as control while rats in Groups 2, 3, 4, and 5 received 100, 200, 400 and 800 mg/kg of Combretum dolichopetalum methanol leaf extract (CDLE) from day 15 to 20 of pregnancy using oral gavage, respectively. Maternal weight, haematological parameters (full blood count), biochemical parameters (renal and liver indices), gestational length, and litter size were measured using standard methods. Results: The result showed a decrease in maternal weight, postpartum weight retained and gestational length, an increase in haematological parameters, and no changes in the renal and liver indices. Conclusion: This study indicates that CDLE during prenatal did not influence the pregnancy outcome but was beneficial in decreasing postpartum weight retained without any visible sign of toxicity.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>459</FPAGE>
			<TPAGE>467</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/262021/04/192021/02/22021/02/72021/02/13
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/11/25
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/282021/09/252021/09/62021/08/312021/10/16
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/7/24
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Chinedum U.</Name>
				<MidName></MidName>
				<Family>Emelike</Family>
				<NameE>Chinedum U.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Emelike</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike, Abakaliki, Ebonyi State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email>chinedum.emelike@funai.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ugochukwu S. B.</Name>
				<MidName></MidName>
				<Family>Anyaehie</Family>
				<NameE>Ugochukwu S. B.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Anyaehie</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medicine, University of Nigeria, Enugu Campus, Enugu, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Eghosa E.</Name>
				<MidName></MidName>
				<Family>Iyare</Family>
				<NameE>Eghosa E.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Iyare</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medicine, University of Nigeria, Enugu Campus, Enugu, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Chiemeziem A.</Name>
				<MidName></MidName>
				<Family>Obike</Family>
				<NameE>Chiemeziem A.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Obike</FamilyE>
				<Organizations>
				<Organization>Department of Biochemistry, Michael Okpara University of Agriculture Umudike, Umuahia, Abia State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Chinyere</Name>
				<MidName></MidName>
				<Family>Aloke</Family>
				<NameE>Chinyere</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Aloke</FamilyE>
				<Organizations>
				<Organization>Department of Medical Biochemistry, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike, Abakaliki, Ebonyi</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ofovwe O.</Name>
				<MidName></MidName>
				<Family>Ekakitie</Family>
				<NameE>Ofovwe O.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ekakitie</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike, Abakaliki, Ebonyi State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>John A. O.</Name>
				<MidName></MidName>
				<Family>Chukwu</Family>
				<NameE>John A. O.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Chukwu</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medicine, Ebonyi State University, Abakaliki, Ebonyi State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ndukwe</Name>
				<MidName></MidName>
				<Family>Maduka</Family>
				<NameE>Ndukwe</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Maduka</FamilyE>
				<Organizations>
				<Organization>Department of Biological Sciences, College of Natural and Applied Sciences, Wellspring University, Benin City, Edo State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Odochi O.</Name>
				<MidName></MidName>
				<Family>Chukwu</Family>
				<NameE>Odochi O.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Chukwu</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Basic Medical Sciences, College of Medical Sciences, Alex Ekwueme Federal University, Ndufu-Alike, Abakaliki, Ebonyi State, Nigeria</Organization>
				</Organizations>
				<Countries>
				<Country>Nigeria</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Combretum dolichopetalum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Biochemical and Haematological parameters</KeyText>
			</KEYWORD>

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

		<REFRENCES>
			<REFRENCE>
				<REF>Ajarem JS and Ahmad M. Effects of perinatal exposure of mice to non-alcoholic malt beverage “beer” on their offspring. Saudi J. Biol. Sci.1998; 5: 78-92##Cheesbrough M. District Laboratory Practice in Tropical Country part II, Second Edition Cambridge University press.2006; 299 - 320.##Chernecky CC, Krech RL and Berger BJ. Laboratory tests and diagonistic procedures. W.B Saunders Company, a division of Harcourt Brace &#38; company, Philadelphia.2003;252-255, 638-639.##Corbette JV. Laboratory tests and diagnostic procedures with nursing diagnoses. 2008; 90-107.##Emelike CU, Ezimah ACU, Anyaehie USB, Iyare EE, Obike CA and Emelike FO. Haematological profile and body mass index of pregnant women in Ndiagu-Echara, Ikwo, Ebonyi State. Proceedings of the FBMS Symposium of Faculty of Basic Medical Sciences, Federal University, Ndufu-Alike.2018; 1: 40-44##Emelike CU, Anyaehie USB, IyareEE, Obike CA, Eleazu COand Chukwuma C.Acute and sub-acute toxicity studies on Combretum dolichopetalum Engl. &#38; Diels leaves.  Slovenian Veterinary Research.2002; 57 (3): 105–114##Emelike CU, Anyaehie USB, Iyare EE, Obike C.A, Aloke, C, Chukwu, DF, Eleazu CO, Chukwu CJ, Ekakitie OO, Konyefom NG and Uzomba CG. Chemical Composition and Evaluation of Methanol Leaf Extract of Combretum dolichopetalum on Body Weights and Haematological Indices of Phenylhydrazine Induced-Anaemic Rats. Toxicology International, 2021; 28 (2) 135-144##	##Ezejiofor CN, Orish CN and Orish EB. Effect of aqueous leaves extract of Costus afer on the liver and kidney of male albino wistar rats. Anc Science Life.2013; 33(1): 4 – 9.##Fogh-Anderson N, Wimberley PD and Thode J. Determination of sodium and potassium with ion-selective electrodes. Clin. Chem.1984; 30:433-436##Gibson PS, Powrie R and Star J. Herbal and alternative medicine use during pregnancy: a cross-sectional survey. Obstetrics &#38;Gynaecology.2004; 97(4), S44-S45##Glover DD, Amonkar M, Rybeck BF and Tracy TS. Prescription, over the counter, and herbal medicine use in a rural, obstetric population. American Journal of Obstetrics and Gynecology. 2003; 188 (4):1039–45##Hollyer T, Boon H, Georgousis A, Smith M and Einarson A. The use of CAM by women suffering from nausea and vomiting during pregnancy. BMC Complementary and Alternative Medicine.2002; 2: 1-6.##Iyare EE and Obaji NN. Effects of aqueous leaf extract of Azadira chtaindica on some haematological parameters and blood glucose level in female rats. Niger J Exp Clin Biosci. 2014; 2:54-58.##Jensen WB. The Origin of Soxhlex Extractor. Journal Chemistry Education.2007; 84 (12):1913-1914 ##Kac G, Benicio MH, Velasquez-Melendez G, Valenta JG and Struchiner CJ. Gestational weight gain and prepregnancy weight influence postpartum weight retention in a cohort of Brazilian women. J. Nutr. Mar. 2004; 134(3):661-666##Kumar M, Manish KG, Anit S and Goel RJ. Healing effects of Musa sapientum var. Paradisiacal in diabetic rats with co-occuring gastric ulcer, cytokines and growth factor by PCR amplification. BMC Complementary and Alternative Medicine.2013; 13: 305.##Maats F, and Crowther C. Patterns of vitamin, mineral and herbal supplement use prior to and during pregnancy. Aust N Z J ObstetGynaecol.2002; 42: 494-496. ##Mallie JP and Boudzoumou P. Functional Renal maturation in rats’ neonates after prenatal exposure to furosemide. Pediatrics Nephrology.1996; 10: 458-460##Nordeng H and Havnen G. Use of herbal drugs in pregnancy: a survey among 400 Norwegian women.Pharmacoepidemiology and Drug Safety.2004; 13: 371-380##Orhue ES, Idu M, Ataman JE and Ebite LE. Haematological and histopathological studies of Jatropha tanjorensis leaves in Rabbits. Asian Journal of Biological Sciences.2008; 1(2): 84-89.##Saliu JA, Elekofehinti OO, Komolafe K and Oboh G. Effects of some green leafy vegetables on the haematological parameters of diabetic rats. Journal of Natural Product Plant Resources.2012; 2(4): 482-485.##Schroder-Van DJP, Vad Der HD, Rokos H, Mareales DG and Kohne J. Synthetic flavonoids cross the plancenta in the rat and are found in the brain. American Journal of Physiology- Endocrinology and Metabolism.1998; 274: E253-E256.##Scott MG, Heusel JW, LeGrys VA and Sigaard-Anderson O. Electrolytes and blood gases [blood gases and pH]. In: Burtis CA, Ashwood ER, eds. Tietz textbook of clinical chemistry, 3rd ed. Philadelphia: WB Saunders.1999; 1072–1088.##Shivaraj G, Prakash BD, Shruthi SK, Vinayak VH, Avinash AK and Sonai NV. Markers of renal function test. N. Am. Journal of Medical Science.2010;2(4): 170 – 173.##Tietz NW. Biochemical assessment of liver function fundamentals of clinical chemistry 4th Edition card A, B, Edward R. A, W. B., Sanders C.1996; 31: 543-548## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of cell-free supernatant of Bifidobacterium bifidum combined with chitosan biodegradable film on full thickness wound healing in rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Wound healing is one of the most critical issues human has been faced since the beginning of creation. Biodegradable polymers are of particular importance. In this study, cell-free supernatant (CFS) of Bifidobacterium bifidum combined with chitosan (CH) film was evaluated as a wound dressing. Methods: Biodegradable films (CH and CFS/CH), as a novel wound dressing, were prepared. For the evaluation of dressing efficacy, 45 male Wistar rats weighing 200-250 g were randomly divided into 3 groups: negative control (without wound treatment), positive control (wound treatment by CH film), and probiotic (wound treatment by CFS/CH film). One full thickness wound was created on the dorsal area of the animals. The wound in positive control and probiotic groups were immediately covered by CH and CFS/CH dressing, respectively. Wound healing process was evaluated by macroscopic observation and histological analysis. During the treatment the expression of IL-1, TGF-B and IL-6 were assayed by qRT-PCR. Results: Our results showed different infiltration patterns of macrophages, fibroblasts, and neutrophils in CFS/CH treated group. Enhanced disposition of collagen and elastin caused improvement of wound healing process by the film. Based on the gene expression results, use of CFS/CH film caused improvement in wound healing kinetic. Conclusion: The biodegradable film based on chitosan and CFS of B. bifidum improves the wound healing process.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>468</FPAGE>
			<TPAGE>479</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2021/04/292021/01/302021/07/22021/05/222021/01/262021/04/192021/02/22021/02/72021/02/132020/07/30
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1399/5/9
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2021/09/252021/08/312021/08/72021/08/72021/11/282021/09/252021/09/62021/08/312021/10/162021/06/21
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1400/3/31
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Atena</Name>
				<MidName></MidName>
				<Family>Bazjou</Family>
				<NameE>Atena</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bazjou</FamilyE>
				<Organizations>
				<Organization>Department of Microbiology, Arak Branch, Islamic Azad University, Arak, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Parvaneh</Name>
				<MidName></MidName>
				<Family>Jafari</Family>
				<NameE>Parvaneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Jafari</FamilyE>
				<Organizations>
				<Organization>Department of Microbiology, Arak Branch, Islamic Azad University, Arak, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>p-jafari@iau-arak.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Azam</Name>
				<MidName></MidName>
				<Family>Marjani</Family>
				<NameE>Azam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Marjani</FamilyE>
				<Organizations>
				<Organization>Department of Chemistry, Arak Branch, Islamic Azad University, Arak, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Neda</Name>
				<MidName></MidName>
				<Family>Akbari</Family>
				<NameE>Neda</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Akbari</FamilyE>
				<Organizations>
				<Organization>Department of Microbiology, Arak Branch, Islamic Azad University, Arak, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Wound healing</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Chitosan</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cell free supernatant</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Biodegradable-film</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Cytokines</KeyText>
			</KEYWORD>
		</KEYWORDS>

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		</REFRENCES>

	</ARTICLE>

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