Anti-oxidative effect of resveratrol on aluminum induced toxicity in rat cerebral tissue

Anti-oxidative effect of resveratrol on aluminum induced toxicity in rat cerebral tissue


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: رسول استخری

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نشریه: 0 , , Issue 5, 2017, , Volume 118 , 2017

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نویسنده ثبت کننده مقاله رسول استخری
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده پزشکی
کد مقاله 61087
عنوان فارسی مقاله Anti-oxidative effect of resveratrol on aluminum induced toxicity in rat cerebral tissue
عنوان لاتین مقاله Anti-oxidative effect of resveratrol on aluminum induced toxicity in rat cerebral tissue
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق) Bratislava Medical Journal
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت http://www.scopus.com/inward/record.url?eid=2-s2.0-85019587222&partnerID=MN8TOARS

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Abstract View references (35) INTRODUCTION: The direct protective effects of resveratrol against oxidative stress have been demonstrated in neuroglial cells, the mechanisms of these effects are not fully understood. The aim of this research was to study the effect of resveratrol on AL induced cerebral injury in rat. METHODS: We divided the groups as follows with 10 animals each: a) Group I - served as control receiving normal drinking water and diet ad libitum. b) Group II - animals were administered aluminum at a dose level of 100 mg/kg body weight for a period of 6 weeks daily through oral gavage. c) Group III - animals were administered aluminum at a dose level of 100 mg/kg body weight and resveratrol at a dose of 10 mg/kg body weight intraperitoneally for a period of 6 weeks daily. After 6 weeks rats were anesthetized and decapitated. Brains were removed immediately and frozen in liquid nitrogen RESULTS: The levels of SOD and GPx antioxidant enzymes were decreased in all of the groups receiving aluminium, but it was less severe in resveratrol treated group. SOD and GPx levels in aluminium + resveratrol group were higher than in the aluminum group (p < 0.05). MDA level, as an index of lipid peroxidation, increased signifi cantly in all of the groups receiving aluminium. MDA level was lower in aluminium + resveratrol group compared to aluminum group and the difference was signifi cant (p < 0.05). CONCLUSIONS: This study suggests that resveratrol is effective in preventing AL induced toxicity by reducing MDA production in cerebral tissue. Resveratrol also attenuated SOD and GPx suppression in cerebral tissue signifi cantly. Our fi ndings provide the rationale for further studies directed to understanding the mechanism of resveratrol in preventing neurodeterioration.

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رسول استخریسوم

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