<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2019</YEAR>
<VOL>23</VOL>
<NO>2</NO>
<MOSALSAL>73</MOSALSAL>
<PAGE_NO>149</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>Neuropharmacological effects of Ocimum basilicum and its constituents</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Various pharmacological effects of Ocimum basilicum (O. basilicum) have been investigated including: antioxidant, antibacterial, anti-ulcerogenic, cardiac stimulant, hypoglycemic, hypolipidemic, hepatoprotective, anti-inflammatory, anticancer and immunomodulatory properties. It has also the beneficial effects in nervous system disorders, reproductive disorders and respiratory diseases. In this article the neuropharmacological effects of O. basilicum and its constituents is reviewed. Methods: The data was gathered by searching: PubMed, Science Direct, Scopus and Google Scholar using the following key words: Basil, O. basilicum, neuropharmacological, neurotoxicity, neurodegeneration, memory, learning, epilepsy, pain, anticonvulsant, antianxiety, anxiety, depression and anti-depressant. Results: This review indicates that O. basilicum and its constituents have various properties including anti-depression, anti-anxiety, anti-analgesic, anti-nociceptive and memory enhancer which are probably due to its antioxidant property of O. basilicum. Conclusion: It seems that O. basilicum and its constituents could be of therapeutic values in nervous system diseases.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>70</FPAGE>
			<TPAGE>81</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/14
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/10/24
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/19
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/29
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Farzaneh</Name>
				<MidName></MidName>
				<Family>Shakeri</Family>
				<NameE>Farzaneh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shakeri</FamilyE>
				<Organizations>
				<Organization>Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mahmoud</Name>
				<MidName></MidName>
				<Family>Hosseini</Family>
				<NameE>Mahmoud</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hosseini</FamilyE>
				<Organizations>
				<Organization>Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Hosseinim@Mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ahmad</Name>
				<MidName></MidName>
				<Family>Ghorbani</Family>
				<NameE>Ahmad</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghorbani</FamilyE>
				<Organizations>
				<Organization>Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>ghorbania@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>O. basilicum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Seizure</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Depression</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Anxiolytic</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Analgesic.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abdoly M, Farnam A, Fathiazad F, Khaki A, Khaki AA, Ibrahimi A, et al.   Antidepressant-like activities of Ocimum basilicum (sweet Basil) in the forced swimming test of rats exposed to electromagnetic field (EMF). Afr J Pharm Pharmacol 2012; 6: 211-15.##Achel DG, Mills R, Otchere J, Achoribo ES, Adu-Bobi NA-K, Donkor S,  et al. Evaluation of the antioxidant potentials of ten leafy vegetables extracts commonly consumed by the Ghanaian population. Elec J Environ Agric Food Chem 2011; 11:85-95.##Adigüzel A, Güllüce M, ŞENGÜL M, Öğütcü H, ŞAHİN F, Karaman I. Antimicrobial effects of Ocimum basilicum (Labiatae) extract. Turkish J Biol 2005; 29:155-60.##Akhtar MS, Munir M.  Evaluation op the gastric antiulcerogenic effects of Solanum nigrum, Brassica oleracea and Ocimum basilicum in rats. J Ethnopharmacol 1989;  27:163-76.##Al-Ghurabi SES. Study the analgesic and sedative effect of Ocimum basilicum alcoholic extract in male rats. Diyala Agric 2014;  1: 1- 6.##Ali S, Abd El Wahab M, Ayuob N, Suliaman M.  The antidepressant-like effect of Ocimum basilicum in an animal model of depression. Biotech Histochem 2017;  92:390-401.##Anaeigoudari A, Hosseini M, Karami R, Vafaee F, Mohammadpour T, Ghorbani A, et al. The effects of different fractions of Coriandrum sativum on pentylenetetrazole-induced seizures and brain tissues oxidative damage in rats. Avicenna J phytomed 2016; 6: 223-35.##Ardeshir Arzi NSK, Ali Javadpour, Maryam Salahcheh. 2015. Study of the Anxiolytic Effect of Ocimum Basilicum Hydroalcoholic Extract in Mice. Res J Pharm Biolo Chem Sci 2015; 6:98-104.##Askari VR, Rahimi VB, Ghorbani A, Rakhshandeh H. Hypnotic Effect of Ocimum basilicum on Pentobarbital-Induced Sleep in Mice. Iran Red Cresc Med J 2016 ;18(7):1-24.##Awad R, Muhammad A, Durst T, Trudeau VL, Arnason JT.  Bioassay‐guided fractionation of lemon balm (Melissa officinalis L.) using an in vitro measure of GABA transaminase activity. Phytother Res 2009; 23:1075-81.##Ayuob NN, El Wahab MGA, Ali SS, Abdel-Tawab HS. Ocimum basilicum improve chronic stress-induced neurodegenerative changes in mice hippocampus. Metabolic Brain Dis 2018; 1-10.##Ayuob NN, Firgany AE-DL, El-Mansy AA, Ali S.  Can Ocimum basilicum relieve chronic unpredictable mild stress-induced depression in mice? Experiment Mol Pathol 2017;  103:153-61.##Eftekhar N, Moghimi A, Boskabady MH, Kaveh M, Shakeri F. Ocimum basilicum affects tracheal responsiveness, lung inflammatory cells and oxidant-antioxidant biomarkers in sensitized rats. Drug Chem Toxicol. 2019;42(3):286-94.##Bilal A, Jahan N, Ahmed A, Bilal SN, Habib S, Hajra S. 2012. Phytochemical and pharmacological studies on Ocimum basilicum Linn-A review. Int J Curr Res Rev 2012 ; 04(23) :73-83.##Blank AF, Santa Rosa YR, de Carvalho Filho JLS, dos Santos CA, de Fátima Arrigoni-Blank M, dos Santos Niculau E, et al. A diallel study of yield components and essential oil constituents in basil (Ocimum basilicum L.). Ind Crops Prod 2012; 38:93-8.##Bora KS, Arora S, Shri R. Role of Ocimum basilicum L. in prevention of ischemia and reperfusion-induced cerebral damage, and motor dysfunctions in mice brain. J Ethnopharmacol 2011; 137:1360-65.##Brar B, Duhan JS, Rakha P. Antidepressant activity of various extract from seed of Ocimum basilicum Linn. Inte J Sci Res 2015; 4:41-3.##Choopankareh S, Vafaee F, Shafei MN, Sadeghnia HR, Salarinia R, Zarepoor L, Hosseini M. Effects of melatonin and theanine administration on pentylenetetrazole-induced seizures and brain tissue oxidative damage in ovariectomized rats. Turkish J Med Sci 2015; 45:842-9.##Choudhury Golak B, Prabhat KJ, Nayak Bhabani S, Panda Sangram K, Tripathy S. Phytochemical investigation and evaluation of analgesic activity of leafy extracts of various Ocimum (tulsi) species. The Indian Pharmacist 2010; 8:67-70.##Dasgupta T, Rao A, Yadava P. Chemomodulatory efficacy of basil leaf (Ocimum basilicum) on drug metabolizing and antioxidant enzymes, and on carcinogen-induced skin and forestomach papillomagenesis. Phytomed  2004; 11:139-51.##Dashputre NL, Naikwade NS. Preliminary immunomodulatory activity of aqueous and ethanolic leaves extracts of Ocimum basilicum Linn in mice. Int J PharmTech Res 2010; 2:1342-9.##Duke JA. 1985. Culinary herbs: A potpourri: Conch Magazine Ltd.##Duke JA, Ayensu ES. 1985. Medicinal plants of China: Reference Publications.##Ebrahimzadeh-Bideskan AR, Mansouri S, Ataei ML, Jahanshahi M, Hosseini M. The effects of soy and tamoxifen on apoptosis in the hippocampus and dentate gyrus in a pentylenetetrazole-induced seizure model of ovariectomized rats. Anat Sci Int 2018; 93:218-30.##Ekambaram SP, Perumal SS, Balakrishnan A, Marappan N, Gajendran SS, Viswanathan V. Antibacterial synergy between rosmarinic acid and antibiotics against methicillin-resistant Staphylococcus aureus. J Intercult Ethnopharmacol 2016; 5:358-65.##Farhang V, Amini J, Ebadollahi A, Sadeghi GR. Ocimum basilicum L. essential oil cultivated in Iran: chemical composition and antifungal activity against three Phytophthora species. Arch Phytopathology Plant Protect 2014; 47:1696-1703.##Gamaro GD, Suyenaga E, Borsoi M, Lermen J, Pereira P, Ardenghi P. Effect of rosmarinic and caffeic acids on inflammatory and nociception process in rats. ISRN pharmacology 2011; 1:1-6.##Hanif MA, Al-Maskari MY, Al-Maskari A, Al-Shukaili A, Al-Sabahi JN. Essential oil composition, antimicrobial and antioxidant activities of unexplored Omani basil. Journal of medicinal plant research 2011; 5(5):751-757.##Hasanein P, Mohammad Zaheri L. Effects of rosmarinic acid on an experimental model of painful diabetic neuropathy in rats. Pharm Biol 2014; 52:1398-1402.##Hussain AI, Anwar F, Sherazi STH, Przybylski R. Chemical composition, antioxidant and antimicrobial activities of basil (Ocimum basilicum) essential oils depends on seasonal variations. Food Chem 2008; 108:986-95.##Ismail M. Central Properties and Chemical Composition of Ocimum basilicum. Essential Oil. Pharm Biol 2006; 44:619-26.##Javanmardi J, Khalighi A, Kashi H, Vivanco JM. Chemical characterization of Basil (Ocimum basilicum L.) found in local accessions and used in traditional medicines in Iran. J Agric Food Chem. 2002; 50: 5878–5883.##Joshi RK. Chemical composition and antimicrobial activity of the essential oil of Ocimum basilicum L.(sweet basil) from Western Ghats of North West Karnataka, India. Ancient science of life; 2014; 33:151.##Karami R, Hosseini M, Mohammadpour T, Ghorbani A, Sadeghnia HR, Rakhshandeh H, et al.  Effects of hydroalcoholic extract of Coriandrum sativum on oxidative damage in pentylenetetrazole-induced seizures in rats. Iran J Neurol 2015; 14:59-66.##Katalinic V, Milos M, Kulisic T, Jukic M. Screening of 70 medicinal plant extracts for antioxidant capacity and total phenols. Food Chem 2006; 94:550-57.##Khaki A. Protective Effect of Ocimum basilicum on Brain Cells Exposed to Oxidative Damage by Electromagnetic Field in Rat: Ultrastructural Study by Transmission Electron Microscopy. Cresc J Med Biol Sci 2016; 3:1-7.##Khodabakhshi T, Beheshti F, Hosseini M, Mousavi SM, Rakhshandeh H, Sadeghnia HR, et al. Effect of Ocimum basilicum hydro-alcoholic extract on oxidative damage of brain tissue following seizures induced by pentylenetetrazole in mice. Physiol Pharmacol  2017; 21:295-303.##Lee HJ, Jeong Y-I, Lee T-H, Jung ID, Lee JS, Lee C-M, et al. Rosmarinic acid inhibits indoleamine 2, 3-dioxygenase expression in murine dendritic cells. Biochem Pharmacol 2007; 73:1412-21.##Loughrin JH, Kasperbauer MJ. Light reflected from colored mulches affects aroma and phenol content of sweet basil (Ocimum basilicum L.) leaves. J Agric Food Chem 2001 ; 49:1331-5.##Marzouk AM. Hepatoprotective triterpenes from hairy root cultures of Ocimum basilicum L. Zeitschrift für Naturforschung C 2009; 64:201-9.##Medeiros Venancio A, Ferreira-da-Silva FW, da Silva-Alves KS, de Carvalho Pimentel H, Macêdo Lima M, Fraga de Santana M, et al . Essential Oil of Ocimum basilicum L. and (−)-Linalool Blocks the Excitability of Rat Sciatic Nerve. Evid Based Complement Alternat Med. 2016; 1:1-7.##El-Azim M, Abdelgawad A, El-Gerby M, Ali S, El-Mesallamy A. Phenolic Compounds and Cytotoxic Activities of Methanol Extract of Basil (Ocimum basilicum L.). J Microb Biochem Technol 2015; 7:182-5.##Min SS, Han SH, Yee J, Kim C, Seol GH, Im JH, et al . Antinociceptive Effects of the Essential Oil of Ocimum Basilicum in Mice. Korean J Pain 2009; 22:206-9.##Modaresi M, Pouriyanzadeh A. Effect of Ocimum Basilicum Hydro Alcoholic Extract Against Pentylenetetrazole-Induced Seizure in Mice. Armaghane danesh 2013; 18:615-21.##Modaresi M, Pouriyanzadeh A, Asadi-Samani M. Antiepileptic activity of hydroalcoholic extract of basil in mice. Journal of HerbMed Pharmacology 2014; 3.##Muneefa K, Doss V, Sowndarya R. Beneficial effect of hydroethanolic extract of Ocimum basilicum L on enzymic and non enzymic antioxidant in depression induced rats. J Med Plants 2017; 5:185-8.##Nascimento SS, Araújo AA, Brito RG, Serafini MR, Menezes PP, DeSantana JM, et al . Cyclodextrin-complexed Ocimum basilicum leaves essential oil increases Fos protein expression in the central nervous system and produce an antihyperalgesic effect in animal models for fibromyalgia. Int J Mol Sci 2014; 16:547-63.##Neamati A, Talebi S, Hosseini M, Hossein Boskabady M, Beheshti F.  Administration of Ethanolic Extract of Ocimum Basilicum Leaves Attenuates Depression Like Behavior in the Rats Sensitized by Ovalbumin. Curr Nutr Food Sci 2016; 12:72-8.##Nemati Z, Oveisi S, Komaki A, Shahidi S. 2015. Anxiolytic Effect of Ocimum basilicum Extract in Rats Tested by Elevated Plus-Maze Task. Avicenna J Neuro Psych Physiol  2015 ; 2(2): 31-6.##Netto JDL, Oliveira RS, Copatti CE. Efficiency of essential oils of Ocimum basilicum and Cymbopogum flexuosus in the sedation and anaesthesia of Nile tilapia juveniles. Anais da Academia Brasileira de Ciências: 2017; 89(4):2971-4.##Oliveira JS, Porto LA, Estevam CS, Siqueira RS, Alves PB, Niculau ES, Blank AF, Almeida RN, Marchioro M, QUINTANS-JÚNIOR LJ. 2009. Phytochemical screening and anticonvulsant property of Ocimum basilicum leaf essential oil. Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas 8.##Omidbeigi, R. Production and processing of medicinal plants; Astan Ghods Razavi Press: Tehran, Iran, 2000; Vol. I, pp 99104.##Pullaiah T. 2006. Encyclopaedia of world medicinal plants: Daya books.##Rabbani M, Sajjadi SE, Vaezi A. 2015. Evaluation of anxiolytic and sedative effect of essential oil and hydroalcoholic extract of Ocimum basilicum L. and chemical composition of its essential oil. Research in pharmaceutical sciences 2015; 10:535-9.##Rameshrad M, Salehian R, Fathiazad F, Hamedeyazdan S, Garjani M, Maleki-Dizaji N, et al. The effects of Ocimum basilicum ethanol extract on carrageenan induced paw inflammation in rats. Pharm Sci 2015; 20:149-55.##Shakeri F, Eftekhar N, Roshan NM, Rezaee R, Moghimi A, Boskabady MH. Rosmarinic acid affects immunological and inflammatory mediator levels and restores lung pathological features in asthmatic rats. Allergol Immunopathol 2019 ;47(1):16-23.##Sarahroodi S, Esmaeili S, Mikaili P, Hemmati Z, Saberi Y. The effects of green Ocimum basilicum hydroalcoholic extract on retention and retrieval of memory in mice. Anc Sci Life. 2012 ;31(4):185-9.##Seghatoleslam M, Alipour F, Shafieian R, Hassanzadeh Z, Edalatmanesh MA, Sadeghnia HR, et al. The effects of Nigella sativa on neural damage after pentylenetetrazole induced seizures in rats. J Tradit Complement Med 2016; 6:262-8.##Shekarchi M, Hajimehdipoor H, Saeidnia S, Gohari AR, Hamedani MP.  Comparative study of rosmarinic acid content in some plants of Labiatae family. Pharmacogn Mag. 2012 ;8(29):37-41.##Simon J, Morales M, Phippen W, Vieira R, Hao Z, Janick J. Perspectives on new crops and new uses. In: A source of aroma compounds and a popular culinary and ornamental herb: ASHS Press Alexandria, 1999; 499-505.##Tadros MG, Ezzat SM, Salama MM, Farag MA. In vitro and in vivo Anticholinesterase Activity of the Volatile Oil of the Aerial Parts of Ocimum basilicum L. and O. africanum Lour. Growing in Egypt 2014; 9997670.##Tsyvunin V, Shtrygol'S Y. Antiepileptic potential of Fumaria schleicheri and Ocimum basilicum dry extracts. Вісник фармації: 2015; 64-68.##Venâncio AM, Marchioro M, Estavam CS, Melo MS, Santana MT, Onofre AS, et al.  Ocimum basilicum leaf essential oil and (-)-linalool reduce orofacial nociception in rodents: a behavioral and electrophysiological approach. Revista Brasileira de Farmacognosia 2011; 21:1043-1051.##Veronica Gradinariu OC, Lucian Hritcu, Adriana Trifan, Elvira Gille, Monica Hancianu. Comparative efﬁcacy of Ocimum sanctum L. and Ocimum basilicum L. essential oils against amyloid beta (1–42)induced anxiety and depression in laboratory rats. Phytochem Rev 2015; 14:567-75.##Zahra K, Khan M, Iqbal F. Oral supplementation of Ocimum basilicum has the potential to improves the locomotory, exploratory, anxiolytic behavior and learning in adult male albino mice. Neurol Sci 2015; 36:73-8.##Zeggwagh N, Sulpice T, Eddouks M. Anti-hyperglycaemic and hypolipidemic effects of Ocimum basilicum aqueous extract in diabetic rats. Am J Pharmacol Toxicol  2007; 2:123-9.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Cobalamin modulate neurotoxic effects of trimethyltin chloride on hippocampus neural cells and cognitive function</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Cobalamin (vitamin B12) is essential for metabolism of the nervous system and its supplementation attenuate neuropathic and neuroinflammatory diseases. We designed to investigate the neuroprotective effects of cobalamin against the trimethyltin chloride (TMT) induced structural and functional damages in the hippocampus. Methods: Adult male Wistar rats were divided into four groups: 1) control: received saline; 2) TMT: received a single dose of TMT (8mg/kg; ip) to induce hippocampal damages; 3) cobalamin: received cobalamin (18mg/kg; ip) for five consecutive days and 4) TMT+cobalamin: received single ip injection of TMT then were treated with cobalamin for five consecutive days. In day six of the experiments, behavioral effects of TMT and cobalamin were evaluated through shuttle box and novel object recognition task. After the behavioral tests, animals were perfused transcardially and Nissl staining was used on hippocampus to assess neural cell damages. Results: Novel object exploring time was significantly decreased in TMT treated rats and treatment with cobalamin after TMT injection significantly recompensed this effect of TMT. In passive avoidance, TMT significantly decreased latency to enter the dark box, while cobalamin administration after the TMT injection significantly abolished this effect of TMT. Neural cell counted in the areas of hippocampus was significantly decreased in the TMT group and cobalamin treatment after the TMT injection significantly prevented neural cell loss. Conclusion: These results indicate a neuroprotective role for cobalamin against the TMT induced memory impairment and hippocampal neuronal loss.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>82</FPAGE>
			<TPAGE>90</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/18
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/11/29
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/24
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Zeinab</Name>
				<MidName></MidName>
				<Family>Hamidizad</Family>
				<NameE>Zeinab</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hamidizad</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Qom University of Medical Sciences, Qom, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Shima</Name>
				<MidName></MidName>
				<Family>Ababzadeh</Family>
				<NameE>Shima</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ababzadeh</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, School of Medicine, Qom University of Medical Sciences, Qom, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Heidari</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Heidari</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, School of Medicine, Qom University of Medical Sciences, Qom, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Narges-al-Sadat</Name>
				<MidName></MidName>
				<Family>Haeri</Family>
				<NameE>Narges-al-Sadat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Haeri</FamilyE>
				<Organizations>
				<Organization>Cellular and Molecular Research Center, Qom University of Medical Sciences, Qom, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohsen</Name>
				<MidName></MidName>
				<Family>Eslami Farsani</Family>
				<NameE>Mohsen</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Eslami Farsani</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, School of Medicine, Qom University of Medical Sciences, Qom, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehdi</Name>
				<MidName></MidName>
				<Family>Sadegh</Family>
				<NameE>Mehdi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sadegh</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>m.sadegh@arakmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Avoidance memory</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Neurotoxin</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Novel Object</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Vitamin B12.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Antunes M, Biala G. The novel object recognition memory: Neurobiology, test procedure, and its modifications. Cognitive processing 2012; 13: 93-110.##Arora K, Sequeira JM, Alarcon JM, Wasek B, Arning E, Bottiglieri T, et al. Neuropathology of vitamin b12 deficiency in the cd320(-/-) mouse. FASEB J 2019; 33: 2563-2573.##Botton PH, Costa MS, Ardais AP, Mioranzza S, Souza DO, da Rocha JBT, et al. Caffeine prevents disruption of memory consolidation in the inhibitory avoidance and novel object recognition tasks by scopolamine in adult mice. Behavioural Brain Research 2010; 214: 254-259.##Chan W, Almasieh M, Catrinescu MM, Levin LA. Cobalamin-associated superoxide scavenging in neuronal cells is a potential mechanism for vitamin b12-deprivation optic neuropathy. Am J Pathol 2018; 188: 160-172.##Choi GN, Kim JH, Kwak JH, Jeong C-H, Jeong HR, Lee U, et al. Effect of quercetin on learning and memory performance in icr mice under neurotoxic trimethyltin exposure. Food Chemistry 2012; 132: 1019-1024.##Corvino V, Marchese E, Michetti F, Geloso MC. Neuroprotective strategies in hippocampal neurodegeneration induced by the neurotoxicant trimethyltin. Neurochemical research 2013; 38: 240-253.##Douaud G, Refsum H, de Jager CA, Jacoby R, Nichols TE, Smith SM, et al. Preventing alzheimer's disease-related gray matter atrophy by b-vitamin treatment. Proc Natl Acad Sci U S A 2013; 110: 9523-8.##Eagle AL, Wang H, Robison AJ. Sensitive assessment of hippocampal learning using temporally dissociated passive avoidance task. Bio-protocol 2016; 6.##Ebrahimpour S, Fazeli M, Mehri S, Taherianfard M, Hosseinzadeh H. Boswellic acid improves cognitive function in a rat model through its antioxidant activity:-neuroprotective effect of boswellic acid. Journal of pharmacopuncture 2017; 20: 10.##Figiel I, Dzwonek K. Tnfα and tnf receptor 1 expression in the mixed neuronal–glial cultures of hippocampal dentate gyrus exposed to glutamate or trimethyltin. Brain research 2007; 1131: 17-28.##Gasparova Z, Stara V, Janega P, Navarova J, Sedlackova N, Mach M, et al. Pyridoindole antioxidant-induced preservation of rat hippocampal pyramidal cell number linked with reduction of oxidative stress yet without influence on cognitive deterioration in alzheimer-like neurodegeneration. Neuroendocrinology Letters 2014; 35.##Geloso MC, Corvino V, Michetti F. Trimethyltin-induced hippocampal degeneration as a tool to investigate neurodegenerative processes. Neurochemistry international 2011; 58: 729-738.##Gunes HN, Bekircan-Kurt CE, Tan E, Erdem-Ozdamar S. The histopathological evaluation of small fiber neuropathy in patients with vitamin b12 deficiency. Acta Neurol Belg 2018; 118: 405-410.##Guo J, Ni S, Li Q, Wang JZ, Yang Y. Folate/vitamin b alleviates hyperhomocysteinemia-induced alzheimer-like pathologies in rat retina. Neurosci Bull 2019; 35: 325-335.##Hajihashemi S, Hamidizad Z, Rahbari A, Ghanbari F, Motealeghi ZA. Effects of cobalamin (vitamin b12) on gentamicin induced nephrotoxicity in rat. Drug research 2017; 67: 710-718.##Hobbenaghi R, Javanbakht J, Hosseini E, Mohammadi S, Rajabian M, Moayeri P, et al. Neuropathological and neuroprotective features of vitamin b12 on the dorsal spinal ganglion of rats after the experimental crush of sciatic nerve: An experimental study (vol 8, pg 123, 2013). Diagnostic Pathology 2016; 11.##Jianhai L, Qian W, Huanhuan H, Xin S, Guodong L, Shuai W, et al. Nlrp3 inflammasome activation is involved in trimethyltin-induced neuroinflammation. Brain Res 2019.##Kaur S, Chhabra R, Nehru B. Ginkgo biloba extract attenuates hippocampal neuronal loss and cognitive dysfunction resulting from trimethyltin in mice. Phytomedicine 2013; 20: 178-186.##Kim J, Kim CY, Oh H, Ryu B, Kim U, Lee JM, et al. Trimethyltin chloride induces reactive oxygen species-mediated apoptosis in retinal cells during zebrafish eye development. Sci Total Environ 2019; 653: 36-44.##Kim YS. Magnolol protects against trimethyltin-induced neuronal damage and glial activation in vitro and in vivo. Neurotoxicology 2016; 53: 173-185.##Kobe T, Witte AV, Schnelle A, Grittner U, Tesky VA, Pantel J, et al. Vitamin b-12 concentration, memory performance, and hippocampal structure in patients with mild cognitive impairment. Am J Clin Nutr 2016; 103: 1045-54.##Kopruszinski CM, Reis RC, Chichorro JG. B vitamins relieve neuropathic pain behaviors induced by infraorbital nerve constriction in rats. Life sciences 2012; 91: 1187-1195.##Lee S, Yang M, Kim J, Kang S, Kim J, Kim J-C, et al. Trimethyltin-induced hippocampal neurodegeneration: A mechanism-based review. Brain research bulletin 2016; 125: 187-199.##Ogita K, Nishiyama N, Sugiyama C, Higuchi K, Yoneyama M, Yoneda Y. Regeneration of granule neurons after lesioning of hippocampal dentate gyrus: Evaluation using adult mice treated with trimethyltin chloride as a model. Journal of neuroscience research 2005; 82: 609-621.##Randaccio L, Geremia S, Demitri N, Wuerges J. Vitamin b12: Unique metalorganic compounds and the most complex vitamins. Molecules 2010; 15: 3228-3259.##Roberts RA, Aschner M, Calligaro D, Guilarte TR, Hanig JP, Herr DW, et al. Translational biomarkers of neurotoxicity: A health and environmental sciences institute perspective on the way forward. Toxicological Sciences 2015; 148: 332-340.##Röhl C, Sievers J. Microglia is activated by astrocytes in trimethyltin intoxication. Toxicology and applied pharmacology 2005; 204: 36-45.##Romano MR, Biagioni F, Carrizzo A, Lorusso M, Spadaro A, Ferrari TM, et al. Effects of vitamin b12 on the corneal nerve regeneration in rats. Experimental eye research 2014; 120: 109-117.##Shin E-J, Suh S, Lim Y, Jhoo W-K, Hjelle O, Ottersen O, et al. Ascorbate attenuates trimethyltin-induced oxidative burden and neuronal degeneration in the rat hippocampus by maintaining glutathione homeostasis. Neuroscience 2005; 133: 715-727.##Shuto M, Higuchi K, Sugiyama C, Yoneyama M, Kuramoto N, Nagashima R, et al. Endogenous and exogenous glucocorticoids prevent trimethyltin from causing neuronal degeneration of the mouse brain in vivo: Involvement of oxidative stress pathways. Journal of pharmacological sciences 2009; 110: 424-436.##Silakhori S, Hosseinzadeh H, Shaebani Behbahani F, Mehri S. Neuroprotective effect of clavulanic acid on trimethyltin (tmt)-induced cytotoxicity in pc12 cells. Drug and chemical toxicology 2018: 1-7.##Smith AD. Hippocampus as a mediator of the role of vitamin b-12 in memory. Am J Clin Nutr 2016; 103: 959-60.##Stabler SP. Vitamin b12 deficiency. New England Journal of Medicine 2013; 368: 149-160.##van de Lagemaat EE, de Groot L, van den Heuvel E. Vitamin b12 in relation to oxidative stress: A systematic review. Nutrients 2019; 11.##Wheatley C. A scarlet pimpernel for the resolution of inflammation? The role of supra-therapeutic doses of cobalamin, in the treatment of systemic inflammatory response syndrome (sirs), sepsis, severe sepsis, and septic or traumatic shock. Medical hypotheses 2006; 67: 124-142.##Wheatley C. The return of the scarlet pimpernel: Cobalamin in inflammation ii—cobalamins can both selectively promote all three nitric oxide synthases (nos), particularly inos and enos, and, as needed, selectively inhibit inos and nnos. Journal of nutritional &#38; environmental medicine 2007; 16: 181-211.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>The effects of captopril on learning and memory impairment induced by scopolamine in rats: anti-oxidative effects</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Angiotensin converting enzyme (ACE) inhibitors are suggested to have some beneficial effects on the brain. In the present study the protective effects against brain tissues oxidative damage as possible mechanism for learning and memory improving effects of captopril was investigated in scopolamine treated rats. Methods: Fifty male Wistar rats were divided into seven groups and treated: saline as a control group, Sco (scopolamine) and Sco-Capto10, 50 and 100 (captopril 10, 50 and 100mg/kg before scopolamine). Treatment was passive avoidance test and then the cortical tissues were collected to measure malondialdehyde (MDA), nitric oxide (NO) metabolites, thiol, super oxide dismutase (SOD) and catalase (CAT). Results: Scopolamine decreased the latency to enter the dark in passive avoidance test compared to control group. It also increased MDA and NO metabolites while decreased thiol, SOD and CAT in comparison with control group. Captopril increased the latency to enter the dark. It also decreased MDA and NO metabolites while, increased thiol, SOD and CAT. Conclusion: Captopril protected brain tissues oxidative damage and improved learning and memory impairment induced by scopolamine.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>91</FPAGE>
			<TPAGE>100</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/9
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/10/19
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/24
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Hamid Reza</Name>
				<MidName></MidName>
				<Family>Akbari</Family>
				<NameE>Hamid Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Akbari</FamilyE>
				<Organizations>
				<Organization>Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farimah</Name>
				<MidName></MidName>
				<Family>Beheshti</Family>
				<NameE>Farimah</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Beheshti</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>beheshtif931@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hamid Reza</Name>
				<MidName></MidName>
				<Family>Sadeghnia</Family>
				<NameE>Hamid Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sadeghnia</FamilyE>
				<Organizations>
				<Organization>Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Sadeghniahr@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Soleyman</Name>
				<MidName></MidName>
				<Family>Bafadam</Family>
				<NameE>Soleyman</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bafadam</FamilyE>
				<Organizations>
				<Organization>Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Yousef</Name>
				<MidName></MidName>
				<Family>Baghcheghi</Family>
				<NameE>Yousef</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Baghcheghi</FamilyE>
				<Organizations>
				<Organization>Student Research Committee, Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Baghchey911@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mahmoud</Name>
				<MidName></MidName>
				<Family>Hosseini</Family>
				<NameE>Mahmoud</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hosseini</FamilyE>
				<Organizations>
				<Organization>Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hosseinim@mumsa.c.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Scopolamine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Captopril</KeyText>
			</KEYWORD>

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

			<KEYWORD>
				<KeyText>Learning and memory.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abareshi A, Anaeigoudari A, Norouzi F, Shafei MN, Boskabady MH, Khazaei M, et al. Lipopolysaccharide-induced spatial memory and synaptic plasticity impairment is preventable by captopril. Adv Med 2016a; 2016: 7676512.##Abareshi A, Hosseini M, Beheshti F, Norouzi F, Khazaei M, Sadeghnia HR, et al. The effects of captopril on lipopolysaccharide induced learning and memory impairments and the brain cytokine levels and oxidative damage in rats. Life Sci 2016b; 167: 46-56.##Abareshi A, Norouzi F, Asgharzadeh F, Beheshti F, Hosseini M, Farzadnia M, et al. Effect of angiotensin-converting enzyme inhibitor on cardiac fibrosis and oxidative stress status in lipopolysaccharide-induced inflammation model in rats. Int J Prev Med 2017; 8:69.##Abdel-Zaher AO, Farghaly HSM, Farrag MMY, Abdel-Rahman MS, Abdel-Wahab BA. A potential mechanism for the ameliorative effect of thymoquinone on pentylenetetrazole-induced kindling and cognitive impairments in mice. Biomed Pharmacother 2017; 88: 553-561.##Aebi H. Catalase in vitro. Methods Enzymol 1984; 105: 121-6.##Anaeigoudari A, Soukhtanloo M, Reisi P, Beheshti F, Hosseini M. Inducible nitric oxide inhibitor aminoguanidine, ameliorates deleterious effects of lipopolysaccharide on memory and long term potentiation in rat. Life Sci 2016; 158: 22-30.##Baghcheghi Y, Hosseini M, Beheshti F, Salmani H, Anaeigoudari A. Thymoquinone reverses learning and memory impairments and brain tissue oxidative damage in hypothyroid juvenile rats. Arq Neuropsiquiatr 2018; 76: 32-40.##Bargi R, Asgharzadeh F, Beheshti F, Hosseini M, Sadeghnia HR, Khazaei M. The effects of thymoquinone on hippocampal cytokine level, brain oxidative stress status and memory deficits induced by lipopolysaccharide in rats. Cytokine 2017; 96: 173-184.##Beatty WW, Butters N, Janowsky DS. Patterns of memory failure after scopolamine treatment: implications for cholinergic hypotheses of dementia. Behav Neural Biol 1986; 45: 196-211.##Beheshti F, Hosseini M, Shafei MN, Soukhtanloo M, Ghasemi S, Vafaee F, et al. The effects of Nigella sativa extract on hypothyroidism-associated learning and memory impairment during neonatal and juvenile growth in rats. Nutr Neurosci 2017; 20: 49-59.##Bild W, Hritcu L, Stefanescu C, Ciobica A. Inhibition of central angiotensin II enhances memory function and reduces oxidative stress status in rat hippocampus. Prog Neuropsychopharmacol Biol Psychiatry 2013; 43: 79-88. ##Bodiga VL, Bodiga S. Renin angiotensin system in cognitive function and dementia. Asian J Neurosci 2013; 2013.##Budzynska B, Boguszewska-Czubara A, Kruk-Slomka M, Skalicka-Wozniak K, Michalak A, Musik I, et al. Effects of imperatorin on scopolamine-induced cognitive impairment and oxidative stress in mice. Psychopharmacology 2015; 232: 931-42.##Ciobica A, Hritcu L, Nastasa V, Padurariu M, Bild W. Inhibition of central angiotensin converting enzyme exerts anxiolytic effects by decreasing brain oxidative stress. J Med Biochem 2011; 30: 109-14.##Collerton D. Cholinergic function and intellectual decline in Alzheimer's disease. Neuroscience 1986; 19: 1-28.##de Cavanagh EM, Inserra F, Ferder L, Fraga CG. Enalapril and captopril enhance glutathione-dependent antioxidant defenses in mouse tissues. Am J Physiol Regul Integr Comp Physiol 2000; 278: R572-7.##Drachman DA. Memory and cognitive function in man: does the cholinergic system have a specific role? Neurology 1977; 27:783-90. ##Drachman DA, Leavitt J. Human memory and the cholinergic system. A relationship to aging?. Arch Neurol 1974; 30: 113-21.##Ebert U, Kirch W. Scopolamine model of dementia: electroencephalogram findings and cognitive performance. Eur J Clin Invest 1998; 28: 944-9.##Fan Y, Hu J, Li J, Yang Z, Xin X, Wang J, et al. Effect of acidic oligosaccharide sugar chain on scopolamine-induced memory impairment in rats and its related mechanisms. Neurosci Lett 2005; 374: 222-6.##Fuld PA. Test profile of cholinergic dysfunction and of Alzheimer-type dementia. J Clin Neuropsychol 1984; 6: 380-92.##Gard PR. The role of angiotensin II in cognition and behaviour. Eur J Pharmacol 2002; 438: 1-14.##Glick SD, Zimmerberg B. Amnesic effects of scopolamine. Behav Biol 1972; 7: 245-54.##Habeeb AF. Reaction of protein sulfhydryl groups with Ellman's reagent. Methods Enzymol 1972; 25: 457-64.##Hasselmo ME. The role of acetylcholine in learning and memory. Curr Opin Neurobiol 2006; 16: 710-5.##Hefco V, Yamada K, Hefco A, Hritcu L, Tiron A, Olariu A, et al. Effects of nicotine on memory impairment induced by blockade of muscarinic, nicotinic and dopamine D2 receptors in rats. Eur J Pharmacol 2003; 474: 227-32.##Hejazian SH, Karimi S, Hosseini M, Mousavi SM, Soukhtanloo M. Protection against brain tissues oxidative damage as a possible mechanism for improving effects of low doses of estradiol on scopolamine-induced learning and memory impairments in ovariectomized rats. Adv Biomed Res 2016; 5: 123.##Hosseini M, Dastghaib SS, Rafatpanah H, Hadjzadeh MA, Nahrevanian H, Farrokhi I. Nitric oxide contributes to learning and memory deficits observed in hypothyroid rats during neonatal and juvenile growth. Clinics (Sao Paulo) 2010; 65: 1175-81.##Hosseini M, Mohammadpour T, Karami R, Rajaei Z, Sadeghnia HR, Soukhtanloo M. Effects of the hydro-alcoholic extract of Nigella sativa on scopolamine-induced spatial memory impairment in rats and its possible mechanism. Chin J Integr Med 2015; 21: 438-44.##Huang F, Buchwald P, Browne CE, Farag HH, Wu WM, Ji F, et al. Receptor binding studies of soft anticholinergic agents. AAPS PharmSci 2001; 3: E30.##Husain K, Hernandez W, Ansari RA, Ferder L. Inflammation, oxidative stress and renin angiotensin system in atherosclerosis. World J Biol Chem 2015; 6: 209-17.##Ishola IO, Adamson FM, Adeyemi OO. Ameliorative effect of kolaviron, a biflavonoid complex from Garcinia kola seeds against scopolamine-induced memory impairment in rats: role of antioxidant defense system. Metab Brain Dis 2017; 32: 235-245.##Kelsey NA, Wilkins HM, Linseman DA. Nutraceutical antioxidants as novel neuroprotective agents. Molecules 2010; 15: 7792-814.##Lenkei Z, Palkovits M, Corvol P, Llorens-Cortes C. Expression of angiotensin type-1 (AT1) and type-2 (AT2) receptor mRNAs in the adult rat brain: a functional neuroanatomical review. Front Neuroendocrinol 1997; 18: 383-439.##Li NC, Lee A, Whitmer RA, Kivipelto M, Lawler E, Kazis LE, et al. Use of angiotensin receptor blockers and risk of dementia in a predominantly male population: prospective cohort analysis. BMJ 2010; 340: b5465.##Luperchio S, Tamir S, Tannenbaum SR. NO-induced oxidative stress and glutathione metabolism in rodent and human cells. Free Radic Biol Med 1996; 21: 513-9.##Madesh M, Balasubramanian KA. A microtiter plate assay for superoxide using MTT reduction method. Indian J Biochem Biophys 1997; 34: 535-9.##McKinley MJ, Albiston AL, Allen AM, Mathai ML, May CN, McAllen RM, et al. The brain renin-angiotensin system: location and physiological roles. Int J Biochem Cell Biol 2003; 35: 901-18.##Mohammadpour T, Hosseini M, Naderi A, Karami R, Sadeghnia HR, Soukhtanloo M, et al. Protection against brain tissues oxidative damage as a possible mechanism for the beneficial effects of Rosa damascena hydroalcoholic extract on scopolamine induced memory impairment in rats. Nutr Neurosci 2015; 18: 329-36.##Nassiri-Asl M, Zamansoltani F, Javadi A, Ganjvar M. The effects of rutin on a passive avoidance test in rats. Prog Neuropsychopharmacol Biol Psychiatry 2010; 34: 204-7.##Pacurari M, Kafoury R, Tchounwou PB, Ndebele K. The Renin-Angiotensin-aldosterone system in vascular inflammation and remodeling. Int J Inflam 2014; 2014: 689360.##Shahveisi K, Mousavi SH, Hosseini M, Rad AK, Jalali SA, Rajaei Z, et al. The role of local renin-angiotensin system on high glucose-induced cell toxicity, apoptosis and reactive oxygen species production in PC12 cells. Iran J Basic Med Sci 2014; 17: 613-21.##Sultana R, Perluigi M, Butterfield DA. Lipid peroxidation triggers neurodegeneration: a redox proteomics view into the Alzheimer disease brain. Free Radic Biol Med 2013; 62: 157-169.##Tabet N, Mantle D, Orrell M. Free radicals as mediators of toxicity in Alzheimer's disease: a review and hypothesis. Adverse Drug React Toxicol Rev 2000; 19: 127-52.##Tabrizian K, Azami K, Belaran M, Soodi M, Abdi K, Fanoudi S, et al. Selective Inducible Nitric Oxide Synthase Inhibitor Reversed Zinc Chloride-Induced Spatial Memory Impairment via Increasing Cholinergic Marker Expression. Biol Trace Elem Res 2016; 173: 443-51.##Tota S, Kamat PK, Saxena G, Hanif K, Najmi AK, Nath C. Central angiotensin converting enzyme facilitates memory impairment in intracerebroventricular streptozotocin treated rats. Behav Brain Res 2012; 226: 317-30.##Uttara B, Singh AV, Zamboni P, Mahajan RT. Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options. Curr Neuropharmacol 2009; 7: 65-74.##Wright JW, Harding JW. The brain angiotensin system and extracellular matrix molecules in neural plasticity, learning, and memory. Prog Neurobiol 2004; 72: 263-93.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Inactivation of β1-adrenergic receptor in the basolateral amygdala nucleus attenuated anxiety-like behaviour in response to foot-shock stress in the male rat</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: The basolateral amygdala (BLA) is implicated in stress-related disorders such as anxiety-like behavior. Substantial data exist demonstrating a close relationship between anxiety and adrenergic receptor function in patients with anxiety disorders; however, little is known about the effects of the &#946;1 adrenergic receptor in the BLA on anxiety. This experiment examined the effects of the &#946;1 adrenergic receptor in the BLA on anxiety-like behavior. Methods: Male Wistar rats were exposed to foot-shock stress four consecutive days that were uncontrollable. The &#946;1-adrenoreceptor agonist (dobutamine; 0.5&#956;l/side) or antagonist (atenolol; 0.25&#956;l/side) bilaterally infused into the BLA five minutes before foot-shock stress. Anxiety-like behaviors were assessed 24h after four consecutive day&#8217;s uncontrollable stress using elevated plus-maze (EPM) and open field test (OFT). Results: Findings of EPM revealed that foot-shock stress leads to anxiogenic effect with reduction the time spent and the number of entries into the open arms and increased head-dipping. Intra-BLA infusions of atenolol before stress affected animal behavior differently, such that it significantly increased the time spent and the number of entries into the open arms and decreased head-dipping. Also, OFT results showed the intra-BLA infusion of atenolol increased the time periods spent in the center, number of center entries and reduced the number of rearing as compared with the stress group. Conclusion: These results suggest that the anxiety-like behavior observed after the foot-shock stress is mediated, in part, by exaggerated &#946;1 adrenergic receptor acting at the BLA.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>101</FPAGE>
			<TPAGE>114</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/92018/11/11
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/8/20
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/142019/04/23
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/3
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Leila</Name>
				<MidName></MidName>
				<Family>Hosseinmardi</Family>
				<NameE>Leila</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hosseinmardi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Islamic Azad University, Damghan Branch, Damghan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>leilahosseinmardi@damghaniau.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Abdolhossein</Name>
				<MidName></MidName>
				<Family>Shiravi</Family>
				<NameE>Abdolhossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shiravi</FamilyE>
				<Organizations>
				<Organization>Department of Biology, Islamic Azad University, Damghan Branch, Damghan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>shiravi@damghaniau.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Gholam Hossein</Name>
				<MidName></MidName>
				<Family>Meftahi</Family>
				<NameE>Gholam Hossein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Meftahi</FamilyE>
				<Organizations>
				<Organization>Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>hossein.meftahi@bmsu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Reza</Name>
				<MidName></MidName>
				<Family>Afarinesh</Family>
				<NameE>Mohammad Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Afarinesh</FamilyE>
				<Organizations>
				<Organization>Kerman Neuroscience Research Center, Institute of Neuropharmachology, Kerman University of Medical Sciences, Kerman, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>r.afarinesh@kmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Anxiety-like behaviour</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Basolateral amygdala</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>β1-Adrenergic receptor</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Stress.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Bali A, Jaggi AS. Electric foot shock stress: a useful tool in neuropsychiatric studies. Rev Neurosci 2015; 26: 655-77. ##Bignante EA, Paglini G, Molina VA. Previous stress exposure enhances both anxiety-like behaviour and p35 levels in the basolateral amygdala complex: modulation by midazolam. Eur Neuropsychopharmacol 2010; 20: 388-97.##Bremner JD, Krystal JH, Southwick SM, Charney DS. Noradrenergic mechanisms in stress and anxiety: II. Clinical studies. Synapse 1996; 23: 39-51.##Bourin M, Petit‐Demoulière B, Dhonnchadha BN, Hascöet M. Animal models of anxiety in mice. Fundam Clin Pharmacol 2007; 21: 567-74.##Buffalari DM, Grace AA. Noradrenergic modulation of basolateral amygdala neuronal activity: opposing influences of alpha-2 and beta receptor activation. J Neurosci 2007; 27: 12358-66.##Calfa G, Volosin M, Molina VA. Glucocorticoid receptors in lateral septum are involved in the modulation of the emotional sequelae induced by social defeat. Behav Brain Res 2006; 172: 324-32.##Castro JE, Varea E, Márquez C, Cordero MI, Poirier G, Sandi C. Role of the amygdala in antidepressant effects on hippocampal cell proliferation and survival and on depression-like behavior in the rat. PloS One 2010; 5: e8618.##Clayton EC, Williams CL. Adrenergic activation of the nucleus tractus solitarius potentiates amygdala norepinephrine release and enhances retention performance in emotionally arousing and spatial memory tasks. Behav Brain Res 2000; 112: 151-8.##Conrad CD, LeDoux JE, Magariños AM, McEwen BS. Repeated restraint stress facilitates fear conditioning independently of causing hippocampal CA3 dendritic atrophy. Behav Neurosci 1999; 113: 902-13.##Davidson RJ. Anxiety and affective style: role of prefrontal cortex and amygdala. Biol Psychiatry 2002; 51: 68-80.##Dimsdale JE, Mills P, Patterson T, Ziegler M, Dillon E. Effects of chronic stress on beta-adrenergic receptors in the homeless. Psychosom Med 1994; 56: 290-5.##Ehteram BZ, Sahraei H, Meftahi GH, Khosravi M. Effect of intermittent feeding on gonadal function in male and female NMRI mice during chronic stress. Braz Arch Biol Technol 2017; 60: e17160607.##Etkin A, Wager TD. Functional neuroimaging of anxiety: a meta-analysis of emotional processing in PTSD, social anxiety disorder, and specific phobia. Am J Psychiatry 2007; 64: 1476-88.##Feinstein JS, Buzza C, Hurlemann R, Follmer RL, Dahdaleh NS, Coryell WH, et al. Fear and panic in humans with bilateral amygdala damage. Nat Neurosci 2013; 16: 270-2.##Felix-Ortiz AC, Beyeler A, Seo C, Leppla CA, Wildes CP, Tye KM. BLA to vHPC inputs modulate anxiety-related behaviors. Neuron 2013; 79: 658-64.##Felix-Ortiz AC, Burgos-Robles A, Bhagat ND, Leppla CA, Tye KM. Bidirectional modulation of anxiety-related and social behaviors by amygdala projections to the medial prefrontal cortex. Neuroscience 2016; 321: 197-209.##Fu A, Li X, Zhao B. Role of beta1-adrenoceptor in the basolateral amygdala of rats with anxiety-like behavior. Brain Res 2008; 1211: 85-92.##Galvez R, Mesches MH, McGaugh JL. Norepinephrine release in the amygdala in response to footshock stimulation. Neurobiol Learn Mem 1996; 66: 253-7.##Hatfield T, Spanis C, McGaugh JL. Response of amygdalar norepinephrine to footshock and GABAergic drugs using in vivo microdialysis and HPLC. Brain Res 1999; 835: 340-5.##Hosoda K, Duman RS. Regulation of beta 1-adrenergic receptor mRNA and ligand binding by antidepressant treatment and norepinephrine depletion in rat frontal cortex. J Neurochem 1993; 60: 1335-43.##Johnson M. The beta-adrenoceptor. Am J Respir Crit Care Med 1998; 158: S146-53.##Kang EH, Yu BH. Anxiety and beta-adrenergic receptor function in a normal population. Prog Neuropsychopharmacol Biol Psychiatry 2005; 29: 733-7.##Kessler RC, Chiu WT, Demler O, Walters EE. Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 2005; 62: 617-27.##LeDoux JE. Emotion circuits in the brain. Ann Rev Neurosci 2000; 23: 155-84.##Lopez AD, Murray CC. The global burden of disease, 1990-2020. Nat Med 1998; 4: 1241-3.##Maj M, Turchan J, Smiałowska M, Przewłocka B. Morphine and cocaine influence on CRF biosynthesis in the rat central nucleus of amygdala. Neuropeptides 2003; 37: 105-10.##Matuszewich L, Karney JJ, Carter SR, Janasik SP, O'brien JL, Friedman RD. The delayed effects of chronic unpredictable stress on anxiety measures. Physiol Behav 2007; 90: 674-81.##McCall JG, Al-Hasani R, Siuda ER, Hong DY, Norris AJ, Ford CP, et al. CRH engagement of the locus coeruleus noradrenergic system mediates stress-induced anxiety. Neuron 2015; 87: 605-20.##McCall JG, Siuda ER, Bhatti DL, Lawson LA, McElligott ZA, Stuber GD, et al. Locus coeruleus to basolateral amygdala noradrenergic projections promote anxiety-like behavior. Elife 2017; 6. pii: e18247.##McEwen BS. Mood disorders and allostatic load. Biol Psychiatry 2003; 54: 200-7.##Mitra R, Ferguson D, Sapolsky RM. SK2 potassium channel overexpression in basolateral amygdala reduces anxiety, stress-induced corticosterone secretion and dendritic arborization. Mol Psychiatry 2009; 14(9): 847–855.##Nagata K, Nakashima-Kamimura N, Mikami T, Ohsawa I, Ohta S. Consumption of molecular hydrogen prevents the stress- induced impairments in hippocampus- dependent learning tasks during chronic physical restraint in mice. Neuropsychopharmacol 2009; 34: 501-8.##Nuttall SL, Routledge HC, Kendall MJ. A comparison of the beta1-selectivity of three beta1-selective beta-blockers. J Clin Pharm Ther 2003; 28: 179-86.##Onur OA, Walter H, Schlaepfer TE, Rehme AK, Schmidt C, Keysers C, et al. Noradrenergic enhancement of amygdala responses to fear. Soc Cogn Affect Neurosci 2009; 4: 119-26.##Paxinos G, Watson C. The rat brain in stereotaxic coordinates. Philadelphia, PA: Elsevier; 5th ed. 2006.##Quirarte GL, Galvez R, Roozendaal B, McGaugh JL. Norepinephrine release in the amygdala in response to footshock and opioid peptidergic drugs. Brain Res 1998; 808: 134-40.##Rauch SL, Shin LM, Wright CI. Neuroimaging studies of amygdala function in anxiety disorders. Ann N Y Acad Sci 2003; 985: 389-410.##Rei D, Mason X, Seo J, Gräff J, Rudenko A, Wang J, et al. Basolateral amygdala bidirectionally modulates stress-induced hippocampal learning and memory deficits through a p25/Cdk5-dependent pathway. Proc Natl Acad Sci U S A 2015; 112: 7291-6.##Rodríguez Manzanares PA, Isoardi NA, Carrer HF, Molina VA. Previous stress facilitates fear memory, attenuates GABAergic inhibition, and increases synaptic plasticity in the rat basolateral amygdala. J Neurosci 2005; 25: 8725-34.##Roozendaal B, Hui GK, Hui IR, Berlau DJ, McGaugh JL, Weinberger NM. Basolateral amygdala noradrenergic activity mediates corticosterone-induced enhancement of auditory fear conditioning. Neurobiol Learn Mem 2006; 86: 249-55.##Roozendaal B, McEwen BS, Chattarji S. Stress, memory and the amygdala. Nat Rev Neurosci 2009; 10: 423-33.##Roszkowski M, Manuella F, von Ziegler L, Durán-Pacheco G, Moreau JL, Mansuy IM, et al. Rapid stress-induced transcriptomic changes in the brain depend on beta-adrenergic signaling. Neuropharmacol 2016; 107: 329-38.##Rudoy CA, Van Bockstaele EJ. Betaxolol, a selective beta(1)-adrenergic receptor antagonist, diminishes anxiety-like behavior during early withdrawal from chronic cocaine administration in rats. Prog Neuropsychopharmacol Biol Psychiatry 2007; 31: 1119-29.##Schiffelers SL, Van Harmelen VJ, De Grauw HA, Saris WH, Van Baak MA. Dobutamine as selective β1-adrenoceptor agonist in in vivo studies on human thermogenesis and lipid utilization. J Appl Physiol 1999; 87: 977-81.##Silberman Y, Ariwodola OJ, Chappell AM, Yorgason JT, Weiner JL. Lateral paracapsular GABAergic synapses in the basolateral amygdala contribute to the anxiolytic effects of β3 adrenoceptor activation. Neuropsychopharmacol 2010; 35: 1886-96.##Siuda ER, Al-Hasani R, McCall JG, Bhatti DL, Bruchas MR. Chemogenetic and optogenetic activation of Gαs signaling in the basolateral amygdala induces acute and social anxiety-like states. Neuropsychopharmacol 2016; 41: 2011-23.##Stahl SM. Basic psychopharmacology of antidepressants, part 1: antidepressants have seven distinct mechanisms of action. J Clin Psychiatry 1998: 59 Suppl 4: 5-14.##Sulser F, Vetulani J, Mobley PL. Mode of action of antidepressant drugs. Biochem Pharmacol 1978; 27: 257-61.##Tanaka M, Yoshida M, Emoto H, Ishii H. Noradrenaline systems in the hypothalamus, amygdala and locus coeruleus are involved in the provocation of anxiety: basic studies. Eur J Pharmacol 2000; 405: 397-406.##Tripathi SJ, Chakraborty S, Srikumar BN, Raju TR, Shankaranarayana Rao BS. Basolateral amygdalar inactivation blocks chronic stress-induced lamina-specific reduction in prefrontal cortex volume and associated anxiety-like behavior. Prog Neuropsychopharmacol Biol Psychiatry 2019; 88: 194-207.##van Eijndhoven P, van Wingen G, van Oijen K, Rijpkema M, Goraj B, Verkes RJ, et al. Amygdala volume marks the acute state in the early course of depression. Biol psychiatry 2009; 65: 812-8.##Walf AA, Frye CA. The use of the elevated plus maze as an assay of anxiety-related behavior in rodents. Nat Protoc 2007; 2: 322-8.##Wei J, Zhong P, Qin L, Tan T, Yan Z. Chemicogenetic restoration of the prefrontal cortex to amygdala pathway ameliorates stress-induced deficits. Cereb Cortex 2017; 28: 1980-1990.##Wohleb ES, Hanke ML, Corona AW, Powell ND, La'Tonia MS, Bailey MT, et al. β-Adrenergic receptor antagonism prevents anxiety-like behavior and microglial reactivity induced by repeated social defeat. J Neurosci 2011; 31: 6277-88.##Wood GE, Young LT, Reagan LP, McEwen BS. Acute and chronic restraint stress alter the incidence of social conflict in male rats. Horm Behav 2003; 43: 205-13.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Insulin attenuates 6-hydroxydopamine induced cell death in human neuroblastoma cells and restores p-Akt/t-Akt level</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Human neuroblastoma cell line is used in studying Parkinson&#8217;s disease (PD) due to its similarities to dopaminergic neurons. 6-hydroxydopamine (6-OHDA), a catecholaminergic neurotoxin, has been widely used to induce cell death in cellular models of PD. Although the brain glucose entry is not dependent on insulin, this peptide has been reported to have a role in PD, in which insulin signaling disruption is reported. This study aimed to evaluate, if insulin is efficient in preventing 6-OHDA induced cell death in human neuroblastoma cells as well as its effect on phoshorylated Akt (p-Akt)/total Akt (t-Akt) ratio. Methods: The cells -grown in DMEM/F12 media supplemented with 10% fetal bovine serum- were exposed to 6-OHDA with/without insulin for 24h, and then MTT assay was done to examine their viability. A pilot study was performed to assess the protective doses of insulin and accordingly the doses 0.9 and 1mM were selected. Western blot assay was done to evaluate the effect of 6-OHDA or insulin on p-Akt and t-Akt level. Results: The results indicated that insulin has potency to prevent SH-SY5Y cell death, and p-Akt/t-Akt decline induced by 6-OHDA. Conclusion: The results suggested insulin as a protective agent in dopaminergic cells.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>115</FPAGE>
			<TPAGE>122</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/92018/11/112018/11/19
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/8/28
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/142019/04/232019/04/16
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/1/27
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<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>stud2282015101@sums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Rasoul</Name>
				<MidName></MidName>
				<Family>Ghasemi</Family>
				<NameE>Rasoul</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghasemi</FamilyE>
				<Organizations>
				<Organization>Neurophysiology Research Center and Department of Physiology, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>Rghasemi60@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>Shiraz Neuroscience 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>Insulin</KeyText>
			</KEYWORD>

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

			<KEYWORD>
				<KeyText>6-OHDA</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>SH-SY5Y</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Akt.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Amiri E, Ghasemi R, Moosavi M. Agmatine protects against 6-OHDA-induced apoptosis, and ERK and Akt/GSK disruption in SH-SY5Y cells. Cell Mol Neurobiol 2016; 36: 829-838.##Ashraghi MR, Pagano G, Polychronis S, Niccolini F, Politis M. Parkinson's disease, diabetes and cognitive impairment. Recent Pat Endocr Metab Immune Drug Discov 2016; 10: 11-21.##Athauda D, Foltynie T. Insulin resistance and Parkinson’s disease: a new target for disease modification?. Prog Neurobiol 2016; 145-146: 98-120.##Bassil F, Fernagut PO, Bezard E, Meissner WG. Insulin, IGF-1 and GLP-1 signaling in neurodegenerative disorders: targets for disease modification?. Prog Neurobiol 2014; 118: 1-18.##Bosco D, Plastino M, Cristiano D, Colica C, Ermio C, De Bartolo M, et al. Dementia is associated with insulin resistance in patients with Parkinson's disease. J Neurol Sci 2012; 315: 39-43.##Canal M, Romaní-Aumedes J, Martín-Flores N, Pérez-Fernández V, Malagelada C. RTP801/REDD1: a stress coping regulator that turns into a troublemaker in neurodegenerative disorders. Front Cell Neurosci 2014; 8: 313.##Chen G, Bower KA, Ma C, Fang S, Thiele CJ, Luo J. Glycogen synthase kinase 3beta (GSK3beta) mediates 6-hydroxydopamine-induced neuronal death. FASEB J 2004; 18: 1162-4.##Cheung YT, Lau WK, Yu MS, Lai CS, Yeung SC, So KF, et al. Effects of all-trans-retinoic acid on human SH-SY5Y neuroblastoma as in vitro model in neurotoxicity research. Neurotoxicology 2009; 30: 127-35.##Curtius HC, Wolfensberger M, Steinmann B, Redweik U, Siegfried J. Mass fragmentography of dopamine and 6-hydroxydopamine. Application to the determination of dopamine in human brain biopsies from the caudate nucleus. J Chromatogr 1974; 99: 529-40.##de Lau LM, Breteler MM. Epidemiology of Parkinson's disease. Lancet Neurol 2006; 5: 525-35.##Esmaeili-Mahani S, Vazifekhah S, Pasban-Aliabadi H, Abbasnejad M, Sheibani V. Protective effect of orexin-A on 6-hydroxydopamine-induced neurotoxicity in SH-SY5Y human dopaminergic neuroblastoma cells. Neurochem Int 2013; 63: 719-25.##Forno LS. Neuropathology of Parkinson's disease. J Neuropathol Exp Neurol 1996; 55: 259-72.##Ghasemi R, Moosavi M, Zarifkar A, Rastegar K, maghsoudi N. The interplay of Akt and ERK in Aβ toxicity and insulin-mediated protection in primary hippocampal cell culture. J Mol Neurosci 2015; 57: 325-34.##Gomez-Lazaro M, Galindo MF, Concannon CG, Segura MF, Fernandez-Gomez FJ, Llecha N, et al. 6-Hydroxydopamine activates the mitochondrial apoptosis pathway through p38 MAPK-mediated, p53-independent activation of Bax and PUMA. J Neurochem 2008; 104: 1599-612.##Greene LA, Levy O, Malagelada C. Akt as a victim, villain and potential hero in Parkinson's disease pathophysiology and treatment. Cell Mol Neurobiol 2011; 31: 969-78.##Hernandez-Baltazar D, Zavala-Flores LM, Villanueva-Olivo A. The 6-hydroxydopamine model and parkinsonian pathophysiology: novel findings in an older model. Neurologia 2017; 32: 533-539.##Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951; 193: 265-75.##Malagelada C, Jin ZH, Greene LA. RTP801 is induced in Parkinson's disease and mediates neuron death by inhibiting Akt phosphorylation/activation. J Neurosci 2008; 28: 14363-71.##Moosavi M, Farrokhi MR, Tafreshi N. The effect of curcumin against 6-hydroxydopamine induced cell death and Akt/GSK disruption in human neuroblastoma cells. Physiol Pharmacol 2018; 22: 163-71.##Moosavi M, Maghsoudi N, Zahedi-Asl S, Naghdi N, Yousefpour M, Trounce IA. The role of PI3/Akt pathway in the protective effect of insulin against corticosterone cell death induction in hippocampal cell culture. Neuroendocrinology 2008; 88: 293-8.##Moosavi M, Zarifkar AH, Farbood Y, Dianat M, Sarkaki A, Ghasemi R. Agmatine protects against intracerebroventricular streptozotocin-induced water maze memory deficit, hippocampal apoptosis and Akt/GSK3β signaling disruption. Eur J Pharmacol 2014; 736: 107-14.##Moroo I, Yamada T, Makino H, Tooyama I, McGeer PL, McGeer EG, et al. Loss of insulin receptor immunoreactivity from the substantia nigra pars compacta neurons in Parkinson's disease. Acta Neuropathologica 1994; 87: 343-8.##Morris JK, Vidoni ED, Perea RD, Rada R, Johnson DK, Lyons K, et al. Insulin resistance and gray matter volume in neurodegenerative disease. Neuroscience 2014; 270: 139-47.##Morris JK, Zhang H, Gupte AA, Bomhoff GL, Stanford JA, Geiger PC. Measures of striatal insulin resistance in a 6-hydroxydopamine model of Parkinson's disease. Brain Res 2008; 1240: 185-95.##Nakaso K, Ito S, Nakashima K. Caffeine activates the PI3K/Akt pathway and prevents apoptotic cell death in a Parkinson's disease model of SH-SY5Y cells. Neurosci Lett 2008; 432: 146-50.##Negintaji K, Zarifkar A, Ghasemi R, Moosavi M. Humanin does not protect against STZ-induced spatial memory impairment. J Mol Neurosci 2015; 56: 290-8.##Nogueira V, Park Y, Chen CC, Xu PZ, Chen ML, Tonic I, et al. Akt determines replicative senescence and oxidative or oncogenic premature senescence and sensitizes cells to oxidative apoptosis. Cancer Cell 2008; 14: 458-70.##Pang Y, Lin S, Wright C, Shen J, Carter K, Bhatt A, et al. Intranasal insulin protects against substantia nigra dopaminergic neuronal loss and alleviates motor deficits induced by 6-OHDA in rats. Neuroscience 2016; 318: 157-65.##Przedborski S. Pathogenesis of nigral cell death in Parkinson's disease. Parkinsonism Relat Disord 2005; 11: Suppl 1:S3-7.##Ramalingam M, Kim SJ. Insulin on hydrogen peroxide-induced oxidative stress involves ROS/Ca2+ and Akt/Bcl-2 signaling pathways. Free Radic Res 2014a; 48: 347-56.##Ramalingam M, Kim SJ. The role of insulin against hydrogen peroxide-induced oxidative damages in differentiated SH-SY5Y cells. J Recept Signal Transduct Res 2014b; 34: 212-20.##Shimoke K, Chiba H. Nerve growth factor prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced cell death via the Akt pathway by suppressing caspase-3-like activity using PC12 cells: relevance to therapeutical application for Parkinson's disease. J Neurosci Res 2001; 63: 402-9.##Storch A, Kaftan A, Burkhardt K, Schwarz J. 6-Hydroxydopamine toxicity towards human SH-SY5Y dopaminergic neuroblastoma cells: independent of mitochondrial energy metabolism. J Neural Transm (Vienna) 2000; 107: 281-93.##Takahashi M, Yamada T, Tooyama I, Moroo I, Kimura H, Yamamoto T, et al. Insulin receptor mRNA in the substantia nigra in Parkinson's disease. Neurosci Lett 1996; 204: 201-4.##van der Heide LP, Ramakers GM, Smidt MP. Insulin signaling in the central nervous system: learning to survive. Prog Neurobiol 2006; 79: 205-21.##Viniegra JG, Martinez N, Modirassari P, Hernandez Losa J, Parada Cobo C, Sanchez-Arevalo Lobo VJ, et al. Full activation of PKB/Akt in response to insulin or ionizing radiation is mediated through ATM. J Biol Chem 2005; 280: 4029-36.##Xie Hr, Hu Ls, Li Gy. SH-SY5Y human neuroblastoma cell line: in vitro cell model of dopaminergic neurons in Parkinson's disease. Chin Med J (Engl) 2010; 123: 1086-92.##Xiromerisiou G, Hadjigeorgiou GM, Papadimitriou A, Katsarogiannis E, Gourbali V, Singleton AB. Association between AKT1 gene and Parkinson's disease: a protective haplotype. Neurosci Lett 2008; 436: 232-4.##Xu Y, Liu C, Chen S, Ye Y, Guo M, Ren Q, et al. Activation of AMPK and inactivation of Akt result in suppression of mTOR-mediated S6K1 and 4E-BP1 pathways leading to neuronal cell death in in vitro models of Parkinson's disease. Cell Signal 2014; 26: 1680-1689.##Yu LY, Pei Y. Insulin neuroprotection and the mechanisms. Chin Med J (Engl) 2015; 128: 976-81.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Ameliorative effect of berberine on functional disorders and histological damages of pancreas in renal ischemia/reperfusion</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Renal ischemia/reperfusion (RIR) is considered as one of the most prevalent reasons of acute renal failure. As renal failure is progressed, renal gluconeogenesis and insulin clearance are decreased. Berberine is the most important alkaloid of Berberis vulgaris. It has anti-diabetic, anti-inflammatory and anti-microbial properties. The goal of this study was to assign the effect of RIR on the pancreas and to define the effect of berberine on the pancreatic damages induced by RIR. Methods: Male rats were allocated into four groups (n=7): sham (no intervention), Ber (berberine, 15mg/kg/day), I/R (subjected to 45min bilateral renal artery occlusion), Ber+I/R (berberine, 15mg/kg/day). After 24h, blood samples were collected for biochemical analysis and eventually pancreas tissue samples were kept for subsequent histological examination. Results: The ischemic challenge of kidneys resulted in pancreatic vascular congestion, which was associated with decreased plasma level of glucose as well as increased plasma insulin, creatinine and blood urea nitrogen levels at the termination of reperfusion period. In Ber+I/R group, pancreatic vascular congestion and decreased plasma level of insulin were improved concomitant to increase in plasma creatinine and urea nitrogen being smaller than those of the non-treated rats. Conclusion: RIR injury has some roles in the development of tissue damages and probably functional disorders of the pancreas in rats. Furthermore, berberine has an ameliorative effect against organ injury induced by RIR in rat.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>123</FPAGE>
			<TPAGE>128</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/92018/11/112018/11/192019/01/5
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/10/15
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/142019/04/232019/04/162019/05/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/24
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Firouzeh</Name>
				<MidName></MidName>
				<Family>Gholampour</Family>
				<NameE>Firouzeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Gholampour</FamilyE>
				<Organizations>
				<Organization>Department of Biology, School of Sciences, Shiraz University, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>gholampour@shirazu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sareh</Name>
				<MidName></MidName>
				<Family>Mansouri</Family>
				<NameE>Sareh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mansouri</FamilyE>
				<Organizations>
				<Organization>Department of Biology, School of Sciences, Shiraz University, Shiraz, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>sa.mansouri@ymail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


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

			<KEYWORD>
				<KeyText>Berberine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pancreas.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abogresha NM, Greish SM, Abdelaziz EZ, Khalil WF. Remote effect of kidney ischemia-reperfusion injury on pancreas: Role of oxidative stress and mitochondrial apoptosis. Arch Med Sci. 2016; 12: 252-62.##Affuso F, Mercurio V, Fazio V, Fazio S. Cardiovascular and metabolic effects of berberine. World J Cardiol. 2010; 2: 71-7.##Arem R. Hypoglycemia associated with renal failure. Endocrinol Metab Clin North Am. 1989; 18: 103-21.##Bonventre JV, Zuk A. Ischemic acute renal failure: An inflammatory disease? Kidney Int. 2004; 66: 480-5.##Brier ME, Aronoff GR, Mayer PR. Effect of acute renal failure on insulin disposition in the isolated perfused rat kidney. Am J Physiol. 1987; 253: F884-8.##D'Apolito M, Du X, Zong H, Catucci A, Maiuri L, Trivisano T, et al. Urea-induced ros generation causes insulin resistance in mice with chronic renal failure. J Clin Invest. 2010; 120: 203-13.##Dennis JM, Witting PK. Protective role for antioxidants in acute kidney disease. Nutrients. 2017; 9: 718.##Derosa G, Maffioli P, Cicero AF. Berberine on metabolic and cardiovascular risk factors: An analysis from preclinical evidences to clinical trials. Expert Opin Biol Ther. 2012; 12: 1113-24.##Friedewald JJ, Rabb H. Inflammatory cells in ischemic acute renal failure. Kidney Int. 2004; 66: 486-91.##Friedman JE, Dohm GL, Elton CW, Rovira A, Chen JJ, Leggett-Frazier N, et al. Muscle insulin resistance in uremic humans: Glucose transport, glucose transporters, and insulin receptors. Am J Physiol Renal Physiol. 1991; 261: E87-94.##Gholampour F, Sadidi Z. Hepatorenal protection during renal ischemia by quercetin and remote ischemic perconditioning. J Surg Res. 2018; 231: 224-233.##Hassoun HT, Grigoryev DN, Lie ML, Liu M, Cheadle C, Tuder RM, et al. Ischemic acute kidney injury induces a distant organ functional and genomic response distinguishable from bilateral nephrectomy. Am J Physiol Renal Physiol. 2007; 293: F30-40.##Hussein AM, Abd-Elkhabir A, Abozahra A, Baiomy A, Ashamallah SA, Sheashaa HA, et al. Pancreatic injury secondary to renal ischemia/reperfusion (i/r) injury: Possible role of oxidative stress. Physiol Res. 2014; 63: 47-55.##Jacobs DB, Hayes GR, Truglia JA, Lockwood DH. Alterations of glucose transporter systems in insulin-resistant uremic rats. Am J Physiol. 1989; 257: E193-7.##Lemay S, Rabb H, Postler G, Singh AK. Prominent and sustained up-regulation of gp130-signaling cytokines and the chemokine mip-2 in murine renal ischemia-reperfusion injury. Transplantation. 2000; 69: 959-63.##Li Z, Geng YN, Jiang JD, Kong WJ. Antioxidant and anti-inflammatory activities of berberine in the treatment of diabetes mellitus. Evid Based Complement Alternat Med. 2014; 2014: 289264.##Liu M, Liang Y, Chigurupati S, Lathia JD, Pletnikov M, Sun Z, et al. Acute kidney injury leads to inflammation and functional changes in the brain. J Am Soc Nephrol 2008; 19: 1360-70.##Meyer C, Dostou JM, Gerich JE. Role of the human kidney in glucose counterregulation. Diabetes. 1999; 48: 943-8.##Mohammadzadeh N, Mehri S, Hosseinzadeh H. Berberis vulgaris and its constituent berberine as antidotes and protective agents against natural or chemical toxicities. Iran J Basic Med Sci. 2017; 20: 538-551.##Sampanis C. Management of hyperglycemia in patients with diabetes mellitus and chronic renal failure. . Hippokratia. 2008; 12: 22-7.##Schmidt C, Hocherl K, Bucher M. Regulation of renal glucose transporters during severe inflammation. Am J Physiol Renal Physiol. 2007; 292: F804-11.##Strenberg SS. Diagnostic surgical pathology. Lippincott Williams &#38; Wilkins, 1996.##Van den Berghe G, Wilmer A, Hermans G, Meersseman W, Wouters PJ, Milants I, et al. Intensive insulin therapy in the medical icu. N Engl J Med.  2006; 354: 449–461.##van den Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, et al. Intensive insulin therapy in the critically ill patients. N Engl J Med. 2001; 345: 1359–1367.##Vriesendorp TM, van Santen S, DeVries JH, de Jonge E, Rosendaal FR, Schultz MJ, et al. Predisposing factors for hypoglycemia in the intensive care unit. Crit Care Med. 2006; 34: 96-101.##Yu W, Sheng M, Xu R, Yu J, Cui K, Tong J, et al. Berberine protects human renal proximal tubular cells from hypoxia/reoxygenation injury via inhibiting endoplasmic reticulum and mitochondrial stress pathways. J Transl Med. 2013; 11: 24.##Zhou H, Mineshita S. The effect of berberine chloride on experimental colitis in rats in vivo and in vitro. J Pharmacol Exp Ther. 2000; 294: 822-9.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Protective effects of Petroselinum crispum on ischemia/reperfusion-induced acute kidney injury in rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Petroselinum crispum (P. crispum) is an associate of Umbelliferae family that has several therapeutic attributes. Ischemia/reperfusion (I/R) is one of the main challenges in acute kidney damage. This study was designed to assess the anti-inflammatory and protective effects of P. crispum extract against I/R-induced renal disorders. Methods: Forty male rats were randomly divided into five groups (n=8) namely normal control (saline) and I/R control group, and three groups of I/R intraperitoneally pretreated with various doses of P. crispum (100, 150 and 200mg/kg). The I/R-induced renal inflammation was evaluated by determining leukocyte infiltration and mRNA expression level of intercellular adhesion molecule-1 and tumor necrotic factor-alpha. Antioxidant capacity of kidneys and thiobarbituric acid reactive species were measured in kidneys for the evaluation of oxidative stress. In addition, the diameters of renal glomeruli, kidney function indicators and serum nitrite oxide levels were respectively determined by morphometric analysis, autoanalyzer device and Griess technique. Results: The I/R increased all measured parameters except for the tissue ferric reducing/antioxidant power (FRAP) level, which was decreased compared to the normal control group. However, pretreatment with P. crispum extract in all doses significantly reduced blood urea nitrogen, kidney malondialdehyde, creatinine, glomerular diameter, leukocyte infiltration, levels of tumor necrotic factor-alpha, adhesion molecule-1 expression, and nitrite oxide as well as increased tissue FRAP compared to the I/R control group. Conclusion: It seems that P. crispum administration improves I/R-induced acute kidney injury.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>129</FPAGE>
			<TPAGE>139</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/92018/11/112018/11/192019/01/52018/12/24
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/10/3
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/142019/04/232019/04/162019/05/142019/05/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/2/24
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Shiva</Name>
				<MidName></MidName>
				<Family>Roshankhah</Family>
				<NameE>Shiva</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Roshankhah</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>roshankhah@kums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Cyrus</Name>
				<MidName></MidName>
				<Family>Jalili</Family>
				<NameE>Cyrus</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Jalili</FamilyE>
				<Organizations>
				<Organization>Medical Biology Research Center, Department of Anatomy, Kermanshah University of Medical Sciences, Kermanshah, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>cjalili@kums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Reza</Name>
				<MidName></MidName>
				<Family>Salahshoor</Family>
				<NameE>Mohammad Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Salahshoor</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mr.salahshour@kums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Petroselinum crispum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Injury</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Kidney.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Ajamieh HH, Menéndez S, Martínez‐Sánchez G, Candelario‐Jalil E, Re L, Giuliani A, et al. Effects of ozone oxidative preconditioning on nitric oxide generation and cellular redox balance in a rat model of hepatic ischaemia-reperfusion. Liver Int 2004; 24: 55-62.##Alhasson F, Seth RK, Sarkar S, Kimono DA, Albadrani MS, Dattaroy D, et al. High circulatory leptin mediated NOX-2-peroxynitrite-miR21 axis activate mesangial cells and promotes renal inflammatory pathology in nonalcoholic fatty liver disease. Redox Biol 2018; 17: 1-15.##Al-Howiriny TA, Al-Sohaibani MO, El-Tahir KH, Rafatullah S. Preliminary evaluation of the anti-inflammatory and anti-hepatotoxic activities of'parsley'petroselinum crispum in rats. J Nat Med 2003; 3: 54-62.##Ali RM, Al-Shorbagy MY, Helmy MW, El-Abhar HS. Role of Wnt4/β-catenin, Ang II/TGFβ, ACE2, NF-κB, and IL-18 in attenuating renal ischemia/reperfusion-induced injury in rats treated with Vit D and pioglitazone. Eur J Pharmacol 2018; 831: 68-76.##Ancuceanu R, Anghel AI, Hovanet MV, Dinu MI, Olaru OT, Dune AL, et al. Variation of iron contents polyphenols and flavonoids in petroselinum crispum (mill) fuss (apiaceae). Farmacia 2018; 66: 275-81.##Byrami G, Boskabady MH, Jalali S, Farkhondeh T. The effect of the extract of Crocus sativus on tracheal responsiveness and plasma levels of IL-4, IFN-γ, total NO and nitrite in ovalbumin sensitized guinea-pigs. J Ethnopharmacol 2013; 147: 530-5.##Corrêa Filho LC, Martinazzo AP, de Souza Teodoro CE, Vivès L. Microbiological quality and essential oil of parsley (Petroselinum crispum) submitted to the hygienizing and drying process. Ind Crop Prod 2018; 114: 180-4.##Cosimi AB, Conti D, Delmonico FL, Preffer FI, Wee SL, Rothlein R, et al. In vivo effects of monoclonal antibody to ICAM-1 (CD54) in nonhuman primates with renal allografts. J Immunol 1990; 144: 4604-12.##Damabi NM, Moazedi AA, Seyyednejad SM. The role of α–and β–adrenergic receptors in the spasmolytic effects on rat ileum of Petroselinum crispum Latifolum (parsley). Asian Pac J Trop Dis 2010; 3: 866-70.##Esfandiari E, Roshankhah S, Mardani M, Hashemibeni B, Naghsh E, Kazemi M, et al. The effect of high frequency electric field on enhancement of chondrogenesis in human adipose-derived stem cells. Iran J Basic Med Sci 2014; 17: 571-6.##Ferdinandy P, Schulz R. Nitric oxide, superoxide, and peroxynitrite in myocardial ischaemia-reperfusion injury and preconditioning. Br J Pharmacol 2003; 138: 532-43.##Ghorbani R, Mokhtari T, Khazaei M, Salahshoor MR, Jalili C, Bakhtiari M. The effect of walnut on the weight, blood glucose and sex hormones of diabetic male rats. Inter J Morphol 2014; 32: 833-8.##Grigoryev DN, Liu M, Hassoun HT, Cheadle C, Barnes KC, Rabb H. The local and systemic inflammatory transcriptome after acute kidney injury. J Am Soc Nephrol 2008; 19: 547-58.##Gupta SC, Kim JH, Prasad S, Aggarwal BB. Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticals. Cancer Metastasis Rev 2010; 29: 405-34.##Haidari F, Keshavarz SA, Mohammad Shahi M, Mahboob SA, Rashidi MR. Effects of parsley (Petroselinum crispum) and its flavonol constituents, kaempferol and quercetin, on serum uric acid levels, biomarkers of oxidative stress and liver xanthine oxidoreductase activity in oxonate-induced hyperuricemic rats. Iran J Pharm Res 2011; 10: 811-9.##Heidari T, Moazedi AA, Seyyednejad SM, Borojeni MP. The role of histaminergic H2 receptors on spasmolytic activity of hydroalcoholic extract of parsley (Petroselinum crispum) seeds in isolated rat’s ileum. J Nat Rem 2018; 17: 114-24.##Jalili C, Makalani F, Roshankhah S, Sohrabi K, Salahshoor MR. Protective effect of resveratrol against morphine damage to kidneys of mice. Int J Morphol 2017; 35: 1409-1415.##Jalili C, Salahshoor MR, Naderi T. The effect of hydroalcoholic extract of P. crispum on sperm parameters, testis tissue and serum nitric oxide levels in mice. Adv Biomed Res 2015; 4: 40.##Jassim AM. Protective effect of Petroselinum crispum (parsley) extract on histopathological changes in liver, kidney and pancreas induced by sodium valproate-in male rats. Kufa j vet Sci 2013; 4: 20-7.##Jia H, Aw W, Hanate M, Takahashi S, Saito K, Tanaka H, et al. Multi-faceted integrated omics analysis revealed parsley (Petroselinum crispum) as a novel dietary intervention in dextran sodium sulphate induced colitic mice. J Funct Foods 2014; 11: 438-48.##Jiang K, Tang H, Mishra PK, Macura SI, Lerman LO. Measurement of murine single‐kidney glomerular filtration rate using dynamic contrast‐enhanced MRI. Magn Reson Med 2018; 79: 2935-43.##Kelly KJ, Williams WW Jr, Colvin RB, Meehan SM, Springer TA, Gutiérrez-Ramos JC, et al. Intercellular adhesion molecule-1-deficient mice are protected against ischemic renal injury. J Clin Invest 1996; 97: 1056-63.##Li QP, Wei RB, Yang X, Zheng XY, Su TY, Huang MJ, et al. Protective effects and mechanisms of shenhua tablet () on Toll-like receptors in rat model of renal ischemia-reperfusion injury. Chin J Integr Med 2019; 25: 37-44.##Mahmoudzadeh L, Najafi H, Ashtiyani SC, Yarijani ZM. Anti-inflammatory and protective effects of saffron extract in ischaemia/reperfusion-induced acute kidney injury. Nephrology (Carlton) 2017; 22: 748-54.##Mitobe M, Yoshida T, Sugiura H, Shirota S, Tsuchiya K, Nihei HOxidative stress decreases klotho expression in a mouse kidney cell line. Nephron Exp Nephrol 2005; 101: e67-74.##Najafi H, Owji SM, Kamali‐Sarvestani E, Moosavi SM. A1 -Adenosine receptor activation has biphasic roles in development of acute kidney injury at 4 and 24 h of reperfusion following ischaemia in rats. Exp Physiol 2016; 101: 913-31.##Nielsen SE, Young JF, Daneshvar B, Lauridsen ST, Knuthsen P, Sandström B, et al. Effect of parsley (Petroselinum crispum) intake on urinary apigenin excretion, blood antioxidant enzymes and biomarkers for oxidative stress in human subjects. Br J Nutr 1999; 81: 447-55.##Park JH, Kho MC, Oh HC, Kim YC, Yoon JJ, Lee YJ. 1,2,3,4,6-penta-O-galloyl-β-D-glucose from Galla rhois ameliorates renal tubular injury and microvascular inflammation in acute kidney injury rats. Am J Chin Med 2018; 46: 785-800.##Perrone S, Weiss MD, Proietti F, Rossignol C, Cornacchione S, Bazzini F, et al. Identification of a panel of cytokines in neonates with hypoxic ischemic encephalopathy treated with hypothermia. Cytokine 2018; 111: 119-124.##Petrolini FV, Lucarini R, de Souza MG, Pires RH, Cunha WR, Martins CH. Evaluation of the antibacterial potential of Petroselinum crispum and Rosmarinus officinalis against bacteria that cause urinary tract infections. Braz J Microbiol 2013; 44: 829-34.##Rabb H, Daniels F, O'Donnell M, Haq M, Saba SR, Keane W, et al. Pathophysiological role of T lymphocytes in renal ischemia-reperfusion injury in mice. Am J Physiol Renal Physiol 2000; 279: F525-31.##Rezazad M, Farokhi F. Protective effect of Petroselinum crispum extract in abortion using prostadin-induced renal dysfunction in female rats. Avicenna J Phytomed 2014; 4: 312.##Rowland LS, Smith HK, Taylor G. The potential to improve culinary herb crop quality with deficit irrigation. Sci Am 2018; 242: 44-50.##Roshankhah SH, Salahshoor MR, Jalili F, Karimi F, Sohrabi M, Jalili C. Crocin effects on the nicotine-induce ovary injuries in female rat. Int J Life Sci Pharma 2017; 7: 1-8.##Salahshoor MR, Khazaei M, Jalili C, Keivan M. Crocin improves damage induced by nicotine on a number of reproductive parameters in male mice. Int J Fertil Steril 2016; 10: 71-8.##Salahshoor MR, Roshankhah S, Hosseni P, Jalili C. Genistein improves liver damage in male mice exposed to morphine. Chin Med J (Engl) 2018; 131: 1598-1604.##Star RA. Treatment of acute renal failure. Kidney Int 1998; 54: 1817-31.##Wong PY, Kitts DD. Studies on the dual antioxidant and antibacterial properties of parsley (Petroselinum crispum) and cilantro (Coriandrum sativum) extracts. Food Chem 2006; 97: 505-15.##Yousofi A, Daneshmandi S, Soleimani N, Bagheri K, Karimi MH. Immunomodulatory effect of Parsley (Petroselinum crispum) essential oil on immune cells: mitogen-activated splenocytes and peritoneal macrophages. Immunopharmacol Immunotoxicol 2012; 34: 303-8.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Ameliorative effects of aqueous cinnamon extract on ulcerative colitis in rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: This study was designed to evaluate the effects of cinnamon extract on ulcerative colitis in rats. Methods: Thirty-two male Wistar rats were divided into four groups: untreated control, positive control group (acetic acid-induced ulcerative colitis), cinnamon extract treated group (150mg/kg/day) and treated group with prednisolone (4mg/kg/day). After 10 consecutive days, the rats were euthanized and examined for the production of inflammatory mediators and oxidative stress indices in the intestinal tissue. Results: Data showed that both therapies could reduce the cumulative disease score. The results also indicated that treatment with cinnamon caused a more benefit in restoring the total antioxidant capacity of the colonic specimens of the colitis-induced rats compared to treatment with prednisolone. The levels of myeloperoxidase and nitric oxide were down-regulated in the colons of cinnamon treated rats more than prednisolone groups. Prednisolone significantly decreased the levels of TNF-&#945; and IL-6 cytokines more than colitis rats treated with cinnamon extract. The levels of COX-2 were decreased and conversely, the total protein content of colonic homogenates was increased in the colons of both treatment groups in a non-significant manner, compared to untreated colitis rats. Conclusion: These results demonstrated cinnamon as herbal medicine is a promising strategy to improve the inflammation in a rat model of ulcerative colitis. It is logical to consider some of the beneficial effects of cinnamon extract associated with its direct antioxidant benefits, along with its direct anti-inflammatory benefits.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>140</FPAGE>
			<TPAGE>149</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2019/01/142019/02/182019/01/92018/11/112018/11/192019/01/52018/12/242019/01/2
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1397/10/12
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2019/05/192019/05/142019/05/142019/04/232019/04/162019/05/142019/05/142019/04/2
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1398/1/13
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Mojtaba</Name>
				<MidName></MidName>
				<Family>Salamatian</Family>
				<NameE>Mojtaba</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Salamatian</FamilyE>
				<Organizations>
				<Organization>Department of Internal Medicine and Clinical Pathology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>mojtaba.salamatian@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Vahid</Name>
				<MidName></MidName>
				<Family>Mohammadi</Family>
				<NameE>Vahid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mohammadi</FamilyE>
				<Organizations>
				<Organization>Department of Internal Medicine and Clinical Pathology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>v.mohammadi@urmia.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Seyyed Meysam</Name>
				<MidName></MidName>
				<Family>Abtahi Froushani</Family>
				<NameE>Seyyed Meysam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Abtahi Froushani</FamilyE>
				<Organizations>
				<Organization>Department of Microbiology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran</Organization>
				</Organizations>
				<Countries>
				<Country>Iran</Country>
				</Countries>
				<EMAILS>
				<Email>sm.abtahi@urmia.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ulcerative colitis</KeyText>
			</KEYWORD>

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

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

		<REFRENCES>
			<REFRENCE>
				<REF>Al-Rejaie SS, Abuohashish HM, Al-Enazi MM, Al-Assaf AH, Parmar MY, Ahmed MM. Protective effect of naringenin on acetic acid-induced ulcerative colitis in rats. World J Gastroenterol 2013; 19: 5633-44.##Auphan N, DiDonato JA, Rosette C, Helmberg A, Karin M. Immunosuppression by glucocorticoids: inhibition of NF-kappa B activity through induction of I kappa B synthesis. Science 1995; 270: 286-90.##Bernstein CN, Fried M, Krabshuis JH, Cohen H, Eliakim R, Fedail S, et al. World Gastroenterology Organization Practice Guidelines for the diagnosis and management of IBD in 2010. Inflamm Bowel Dis 2010; 16: 112-24.##Bryan NS, Grisham MB. Methods to detect nitric oxide and its metabolites in biological samples. Free Radic Biol Med 2007; 43: 645-57.##Chakrabarti S, Jana M, Roy A, Pahan K. Upregulation of suppressor of cytokine signaling 3 in microglia by cinnamic acid. Curr Alzheimer Res 2018; 15: 894-904.##Chen YF, Wang YW, Huang WS, Lee MM, Wood WG, Leung YM, et al. Trans-cinnamaldehyde, an essential oil in cinnamon powder, ameliorates cerebral ischemia-induced brain injury via inhibition of neuroinflammation through attenuation of iNOS, COX-2 expression and NFκ-B signaling pathway. Neuromolecular Med 2016; 18: 322-33.##Clemett D, Goa KL. Celecoxib: a review of its use in osteoarthritis, rheumatoid arthritis and acute pain. Drugs 2000; 59: 957-80.##Consalvi S, Biava M, Poce G. Cox inhibitors: a patent review (2011 - 2014). Expert Opin Ther Pat 2015; 25: 1357-71.##Fabia R, Ar'Rajab A, Johansson ML, Andersson R, Willén R, Jeppsson B, et al. Impairment of bacterial flora in human ulcerative colitis and experimental colitis in the rat. Digestion 1993; 54: 248-55.##Froushani SM, Mashouri S. The beneficial effects of hypiran in ameliorating rat model of ulcerative colitis. Zahedan J Res Med Sci 2018; 20, e58919.##Gao Y, Huang Y, Zhao Y, Hu Y, Li Z, Guo Q, et al. LL202 protects against dextran sulfate sodium-induced experimental colitis in mice by inhibiting MAPK/AP-1 signaling. Oncotarget 2016; 7: 63981-63984.##Gupta RA, Motiwala MN, Mahajan UN, Sabre SG. Protective effect of Sesbania grandiflora on acetic acid induced ulcerative colitis in mice by inhibition of TNF-α and IL-6. J Ethnopharmacol 2018; 219: 222-232.##Hajimonfarednejad M, Ostovar M, Raee MJ, Hashempur MH, Mayer JG, Heydari M. Cinnamon: a systematic review of adverse events. Clin Nutr 2019; 38: 594-602.##Joshi R, Kumar S, Unnikrishnan M, Mukherjee T. Free radical scavenging reactions of sulfasalazine, 5-aminosalicylic acid and sulfapyridine: mechanistic aspects and antioxidant activity. Free Radic Res 2005; 39: 1163-72.##Kim ME, Na JY, Lee JS. Anti-inflammatory effects of trans-cinnamaldehyde on lipopolysaccharide-stimulated macrophage activation via MAPKs pathway regulation. Immunopharmacol Immunotoxicol 2018; 40: 219-224.##Kim SH, Hyun SH, Choung SY. 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