The Effect of Elaeagnus Angustifolia Water Extract on Scopolamine-Induced Memory Impairment in Rats

Publish Year: 1393
نوع سند: مقاله ژورنالی
زبان: English
View: 329

This Paper With 11 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_ZUMS-22-95_010

تاریخ نمایه سازی: 11 اردیبهشت 1400

Abstract:

Background and Objective: Impaired cognitive function and memory, a characteristic of Alzheimerchr('۳۹')s disease, can be caused by decreased activity of the cholinergic system. Scopolamine, a muscarinic receptor antagonist, may cause temporary impairment in memory and provide an Alzheimerchr('۳۹')s disease model. This study was designed to evaluate the effects of water extract of Elaeagnus Angustifolia on memory impairment caused by scopolamine. Materials and Methods: ۶۰ male Wistar rats were randomly assigned to ۶ groups (n=۱۰ for each group). Four groups received scopolamine (۱mg/kg, IP) and water extract of Elaeagnus Angustifolia (۵۰, ۱۰۰, ۲۰۰ and ۴۰۰ mg/kg) along with a positive control group (received scopolamine) and a negative control group. Water extract of Elaeagnus Angustifolia was administered through gavage every day for ۴ weeks. Using Morris water maze (MWM), spatial learning and memory were evaluated. Results: The present study showed that Scopolamine injection leads to impairment of learning and memory of rats in the Morris water test (P<۰.۰۰۰۱). In addition, Elaeagnus Angustifolia water extracts dose-dependently improved the learning and memory impairment induced by scopolamine in rats (P<۰.۰۰۰۱). There was no significant difference between groups that received water extract of Elaeagnus Angustifolia and negative control group (P=۱). Conclusion: Water extract of Elaeagnus Angustifolia improves spatial learning and memory induced by scopolamine in rats. References ۱- Hampel H, Prvulovic D, Teipel S, et al. The future of Alzheimerchr('۳۹')s disease: the next ۱۰ years. Prog Neurobiol. ۲۰۱۱ ۹۵(۴): ۷۱۸-۲۸. ۲- Selkoe DJ. Alzheimerchr('۳۹')s disease: genes, proteins, and therapy. Physiol Rev. ۲۰۰۱ ۸۱(۲): ۷۴۱-۶۶. ۳- Vassar R, Bennett BD, Babu-Khan S, et al. β-Secretase cleavage of Alzheimerchr('۳۹')s amyloid precursor protein by the transmembrane aspartic protease BACE. Science. ۱۹۹۹ ۲۸۶(۵۴۴۰): ۷۳۵-۴۱. ۴-Hernandez F, Avila J. Tauopathies. Cell Mol Life Sci. ۲۰۰۷ ۶۴(۱۷): ۲۲۱۹-۳۳. ۵- Zhu X, Raina AK, Lee H-g, et al. Oxidative stress signalling in Alzheimerchr('۳۹')s disease. Brain Res. ۲۰۰۴ ۱۰۰۰(۱): ۳۲-۹. ۶- Ferreira A, Proença C, Serralheiro M, et al. The in vitro screening for acetylcholinesterase inhibition and antioxidant activity of medicinal plants from Portugal. J Ethnopharmacol. ۲۰۰۶ ۱۰۸(۱): ۳۱-۷. ۷- Walker LC, Rosen RF. Alzheimer therapeutics-what after the cholinesterase inhibitors? Age and ageing. ۲۰۰۶ ۳۵(۴): ۳۳۲-۵. ۸- Ahmed T, Gilani A-H. Inhibitory effect of curcuminoids on acetylcholinesterase activity and attenuation of scopolamine-induced amnesia may explain medicinal use of turmeric in Alzheimerchr('۳۹')s disease. Pharmacol Biochem Behav. ۲۰۰۹ ۹۱(۴): ۵۵۴-۹. ۹- Ebert U, Kirch W. Scopolamine model of dementia: electroencephalogram findings and cognitive performance. Eur J Clin Invest. ۱۹۹۸ ۲۸: ۹۴۴-۹. ۱۰- Murray C, Fibiger H. Pilocarpine and physostigmine attenuate spatial memory impairments produced by lesions of the nucleus basalis magnocellularis. Behav Neurosci. ۱۹۸۶ ۱۰۰(۱): ۲۳. ۱۱- Lee YK, Yuk DY, Kim TI, et al. Protective effect of the ethanol extract of Magnolia officinalis and ۴-O-methylhonokiol on scopolamine-induced memory impairment and the inhibition of acetylcholinesterase activity. J Nat Med. ۲۰۰۹ ۶۳(۳): ۲۷۴-۸۲. ۱۲- Rubio J, Dang H, Gong M, et al. Aqueous and hydroalcoholic extracts of Black Maca (Lepidium meyenii) improve scopolamine-induced memory impairment in mice. Food Chem Toxicol. ۲۰۰۷ ۴۵(۱۰): ۱۸۸۲-۹۰. ۱۳- Kwon S-H, Lee H-K, Kim J-A, et al. Neuroprotective effects of chlorogenic acid on scopolamine-induced amnesia via anti-acetylcholinesterase and anti-oxidative activities in mice. Eur J Pharmacol. ۲۰۱۰ ۶۴۹(۱): ۲۱۰-۷. ۱۴- Richetti S, Blank M, Capiotti K, et al. Quercetin and rutin prevent scopolamine-induced memory impairment in zebrafish. Behav Brain Res. ۲۰۱۱ ۲۱۷(۱): ۱۰-۵. ۱۵- Gacar N, Mutlu O, Utkan T, et al. Beneficial effects of resveratrol on scopolamine but not mecamylamine induced memory impairment in the passive avoidance and Morris water maze tests in rats. Pharmacol Biochem Behav. ۲۰۱۱ ۹۹(۳): ۳۱۶-۲۳. ۱۶- Yoo DY, Choi JH, Kim W, et al. Effects of luteolin on spatial memory, cell proliferation, and neuroblast differentiation in the hippocampal dentate gyrus in a scopolamine-induced amnesia model. Neurol Res. ۲۰۱۳ ۳۵(۸): ۸۱۳-۲۰. ۱۷- Dong J, Sheng Q, Lu D. Effect of curcumin on scopolamine-induced memory impairment in mice. Zhongguo Bingli Shengli Zazhi. ۲۰۰۹ ۲۵(۱): ۱۱۲-۷. ۱۸- Tsai F-S, Peng W-H, Wang W-H, et al. Effects of luteolin on learning acquisition in rats: involvement of the central cholinergic system. Life Sci. ۲۰۰۷ ۸۰(۱۸): ۱۶۹۲-۸. ۱۹- Mirhydar H. Encyclopedia of plants: indications of plants in the prevention and treatment of diseases. Islamic Farhang: Tehran ۱۹۹۸ ۲: ۱۶۳-۴. ۲۰- Hosseinzadeh H, Ramezani, M. and Namjo, N. Muscle relaxant activity of Elaeagnus angustifolia L. fruit seeds in mice. J Ethnopharmacol. ۲۰۰۳ ۸۴(۲-۳): ۲۷۵-۸. ۲۱- Ahmadiani A HJ, Semnanian S, Javan M, et al. Antinociceptive and anti-inflammatory effects of Elaeagnus angustifolia fruit extract. J Ethnopharmacol. ۲۰۰۰ ۷۲(۱-۲): ۲۸۷-۹۲. ۲۲- Ayaz FA, Bertoft E. Sugar and phenolic acid composition of stored commercial oleaster fruits. J Food Compost Anal. ۲۰۰۱ ۱۴(۵): ۵۰۵-۱۱. ۲۳- Bhattamisra SK, Singh PN, Singh SK. Effect of standardized extract of Marsilea minuta on learning and memory performance in rat amnesic models. Pharm Biol. ۲۰۱۲ ۵۰(۶): ۷۶۶-۷۲. ۲۴- Arvouet-Grand A, Vennat B, Pourrat A, et al. Standardization of a propolis extract and identification of the main constituents. J Pharm Belg. ۱۹۹۴ ۴۹: ۴۶۲-۸. ۲۵- Singleton VL, Orthofer R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of folin-ciocalteu reagent. Methods Enzymol. ۱۹۹۹ ۲۹۹: ۱۵۲-۷۸. ۲۶- EL Omri A, Han J, Kawada K, et al. Luteolin enhances cholinergic activities in PC۱۲ cells through ERK۱/۲ and PI۳K/Akt pathways. Brain Res. ۲۰۱۲ ۱۴۳۷: ۱۶-۲۵. ۲۷- Peeyush KT, Gireesh G, Jobin M, et al. Neuroprotective role of curcumin in the cerebellum of streptozotocin-induced diabetic rats. Life Sci. ۲۰۰۹ ۸۵(۱۹): ۷۰۴-۱۰. ۲۸- Yamada N, Hattori A, Hayashi T, et al. Improvement of scopolamine-induced memory impairment by ajoene in the water maze in mice. Pharmacol Biochem Behav. ۲۰۰۴ ۷۸(۴): ۷۸۷-۹۱. ۲۹- Thal L, Fuld P, Masur D, et al. Oral physostigmine and lecithin improve memory in Alzheimer disease. Ann Neurol. ۱۹۸۳ ۱۳(۵): ۴۹۱-۶. ۳۰- Bejar C, Wang R-H, Weinstock M. Effect of rivastigmine on scopolamine-induced memory impairment in rats. Eur J Pharmacol. ۱۹۹۹ ۳۸۳(۳): ۲۳۱-۴۰. ۳۱- Chung JH, Kim M, Kim HK. Green tea polyphenols suppress nitric oxide–induced apoptosis and acetylcholinesterase activity in human neuroblastoma cells. Nutr Res. ۲۰۰۵ ۲۵(۵): ۴۷۷-۸۳. ۳۲- Schmatz R, Mazzanti CM, Spanevello R, et al. Resveratrol prevents memory deficits and the increase in acetylcholinesterase activity in streptozotocin-induced diabetic rats. Eur J Pharmacol. ۲۰۰۹ ۶۱۰(۱): ۴۲-۸. ۳۳- Jain NK, Patil C, Kulkarni SK, et al. Modulatory role of cyclooxygenase inhibitors in aging-and scopolamine or lipopolysaccharide-induced cognitive dysfunction in mice. Behav Brain Res. ۲۰۰۲ ۱۳۳(۲): ۳۶۹-۷۶. ۳۴- Lee KW, Kundu JK, Kim SO, et al. Cocoa polyphenols inhibit phorbol ester-induced superoxide anion formation in cultured HL-۶۰ cells and expression of cyclooxygenase-۲ and activation of NF-κB and MAPKs in mouse skin in vivo. J Nutr. ۲۰۰۶ ۱۳۶(۵): ۱۱۵۰-۵. ۳۵- Liang Y-C, Huang Y-T, Tsai S-H, et al. Suppression of inducible cyclooxygenase and inducible nitric oxide synthase by apigenin and related flavonoids in mouse macrophages. Carcinogenesis. ۱۹۹۹ ۲۰(۱۰): ۱۹۴۵-۵۲.

Authors

امیدرضا تمتاجی

Research Center for Biochemistry and Nutrition in Metabolic Diseases, Students Research Committee, Kashan University of Medical Sciences, Kashan, IR. Iran.

محسن تقیزاده

Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, IR. Iran.

سید مهدی تخت فیروزه

Students Research Committee, Kashan University of Medical Sciences, Kashan, IR. Iran.

سید علیرضا طلایی

Physiology Research Center, Kashan University of Medical Sciences, Kashan, IR. Iran.