Repository of Research and Investigative Information

Repository of Research and Investigative Information

Baqiyatallah University of Medical Sciences

Protective effects of captopril and valsartan on memory function and gene expression of brain-derived neurotrophic factor (BDNF) in experimental model of alzheimer’s disease in rats

(2015) Protective effects of captopril and valsartan on memory function and gene expression of brain-derived neurotrophic factor (BDNF) in experimental model of alzheimer’s disease in rats. Journal of Zanjan University of Medical Sciences and Health Services. ISSN 16069366 (ISSN)

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Protective effects of captopril and valsartan on memory function and gene expression of brain-derived neurotrophic factor (BDNF) in experimental model of alzheimer’s disease in rats.pdf

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Abstract

Background and Objective: The use of ATI and ACE inhibitors, as antihypertensive drugs, improves memory function in the elderly people with hypertension and vulnerable to Alzheimer’s disease (AD). Therefore, the aim of this study was to evaluate effects of oral administration of Captopril and Valsartan on memory function anc expression of brain-derived neurotrophic factor (BDNF) in experimental model of AD in rats. Materials and Methods: Forty adult male Wistar rats were assigned to five groups; Control, Vehicle, Alzheimer, Captopril and Valsartan treated groups. AD in the Alzheimer and treated groups was induced using bilateral i.c.v injection of streptozotocin (3mg/kg) in days one and three. Treated groups received captopril (50mg/kg) and valsartan (30mg/kg) orally for 25days. At the end of the experiment, memory function was tested using T-Mazi and gene expression of BDNF was assessed by RT-PCR technique. Finally, histopathological damages wen evaluated using H&E and toluidine blue staining methods. Results: Time of latency and error number for food searching was 73.4±15.5Sec and 11.8±1.2 in the control group respectively, induction of AD significantly increased these issues (216.2±57.9Sec, 16.2±2.9). Histopathologica damages (necrotic neurons and tissue vacuolization) along with reduction of BDNF mRNA were obviously observed in rats of the Alzheimer group. Captopril and valsartan treatment led to a decrease in the time of latency (46 and 86) and error number (31 and 43) and improved histopathological damages and increased BDNF mRNA. Conclusion: Our findings indicated that inhibition of central renin-angiotensin improves memory function and neuronal damages during AD disease. It appears that activation of this system inhibits gene expression of BDNF. © 2015 Zanjan University of Medical Sciences and Health Services.

Item Type: Article
Keywords: Alzheimer’s Disease BDNF Captopril Renin-angiotensin System Valsartan brain derived neurotrophic factor messenger RNA streptozocin adult Alzheimer disease animal experiment animal model Article controlled study food gene expression histopathology latent period male memory nerve cell lesion nonhuman rat renin angiotensin aldosterone system reverse transcription polymerase chain reaction T-maze test
Divisions:
Journal or Publication Title: Journal of Zanjan University of Medical Sciences and Health Services
Journal Index: Scopus
Volume: 23
Number: 100
ISSN: 16069366 (ISSN)
Depositing User: مهندس مهدی شریفی
URI: http://eprints.bmsu.ac.ir/id/eprint/434

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