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褪黑素可阻断镉诱导的大鼠氧化应激相关神经毒性。

Melatonin abrogates cadmium induced oxidative stress related neurotoxicity in rats.

机构信息

Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Annamalainagar, India.

出版信息

Eur Rev Med Pharmacol Sci. 2011 Sep;15(9):1039-50.

Abstract

BACKGROUND

Cadmium is a potent neurotoxic heavy metal, which induces oxidative stress and membrane disturbances in brain. Melatonin is an effective antioxidant and free radical scavenger against oxidative stress. The present study was designed to investigate the neuroprotective efficacy of melatonin in protecting the Cd induced changes in the activity of acetylcholinesterase (AChE), levels of lipid peroxidation, protein carbonyls, non-enzymatic antioxidant, enzymatic antioxidant status, membrane bound ATPases and histopathology in the brain of rats.

MATERIALS AND METHODS

Twenty four male albino rats were used. Cadmium induced oxidative neurotoxicity was induced by oral administration of Cd for four weeks. Melatonin was pretreated along with Cd for four weeks to assess its neuroprotective activity against Cd intoxication. Rats treated with vehicles alone were used as controls.

RESULTS

Rats intoxicated with cadmium (5 mg/kg/day) for 4 weeks significantly (p < 0.05) reduced the AChE levels in the plasma and brain, elevated the levels of thiobarbituric acid reactive substances (TBARS), lipid hydroperoxides and protein carbonyls along with the significant (p < 0.05) decrease in the levels of non-enzymatic antioxidants (GSH, TSH and vitamins C and E), enzymatic antioxidants superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione S-transferase (GST) and membrane bound ATPases in the brain tissue. Administration of melatonin (10 mg/kg/day) for 4 weeks in cadmium intoxicated rats significantly (p < 0.05) diminished the levels of oxidative stress markers, lipid peroxidation and protein carbonyls in brain and significantly (p < 0.05) elevated the levels of nonenzymatic and enzymatic antioxidants, brain and the activities of AChE, enzymatic antioxidants and ATPases in brain. The histopathological studies in the brain of rats also supported that melatonin markedly reduced the Cd induced pathological changes and preserved the normal histological architecture of the brain tissue.

CONCLUSIONS

The results of the present study suggest that melatonin may be beneficial in combating the cadmium induced oxidative neurotoxicity in the brain of rats.

摘要

背景

镉是一种有效的神经毒性重金属,可引起大脑氧化应激和膜紊乱。褪黑素是一种有效的抗氧化剂和自由基清除剂,可对抗氧化应激。本研究旨在探讨褪黑素对保护大鼠大脑中乙酰胆碱酯酶(AChE)活性、脂质过氧化、蛋白羰基、非酶抗氧化剂、酶抗氧化状态、膜结合 ATP 酶和组织病理学变化的神经保护作用。

材料和方法

使用 24 只雄性白化大鼠。通过口服 Cd 四周诱导 Cd 诱导的氧化神经毒性。褪黑素与 Cd 一起预处理四周,以评估其对 Cd 中毒的神经保护活性。单独用载体处理的大鼠用作对照。

结果

用 Cd(5mg/kg/天)处理 4 周的大鼠显着(p <0.05)降低了血浆和大脑中的 AChE 水平,升高了丙二醛反应性物质(TBARS)、脂质过氧化物和蛋白羰基的水平,同时显着(p <0.05)降低了非酶抗氧化剂(GSH、TSH 和维生素 C 和 E)、酶抗氧化剂超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽 S-转移酶(GST)和脑组织中的膜结合 ATP 酶。4 周给予褪黑素(10mg/kg/天)显着(p <0.05)降低了大脑中氧化应激标志物、脂质过氧化和蛋白羰基的水平,显着(p <0.05)提高了非酶和酶抗氧化剂、大脑和 AChE、酶抗氧化剂和 ATP 酶的水平在大脑中。大鼠大脑的组织病理学研究也表明,褪黑素显着减少了 Cd 诱导的病理变化,保持了脑组织的正常组织学结构。

结论

本研究结果表明,褪黑素可能有助于对抗大鼠大脑中 Cd 诱导的氧化神经毒性。

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