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α-硫辛酸对血管性痴呆大鼠模型空间学习记忆、氧化应激及中枢胆碱能系统的影响

Effects of alpha-lipoic acid on spatial learning and memory, oxidative stress, and central cholinergic system in a rat model of vascular dementia.

作者信息

Zhao Ran-Ran, Xu Fei, Xu Xiao-Chen, Tan Guo-Jun, Liu Liang-Min, Wu Ning, Zhang Wen-Zhong, Liu Ji-Xiang

机构信息

Department of Emergency, The First Hospital of Handan, Handan, Hebei 056002, PR China; Key Laboratory of Neurology of Hebei Province, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei 050071, PR China.

Department of Neurology, The First Hospital of Handan, Handan, Hebei 056002, PR China.

出版信息

Neurosci Lett. 2015 Feb 5;587:113-9. doi: 10.1016/j.neulet.2014.12.037. Epub 2014 Dec 19.

Abstract

Brain oxidative stress due to chronic cerebral hypoperfusion was considered to be the major risk factor in the pathogenesis of vascular dementia. In this study, we investigated the protective efficacy of alpha-lipoic acid, an antioxidant, against vascular dementia in rats, as well as the potential mechanism. Bilateral common carotid arteries occlusion (BCCAO) induced severe cognitive deficits tested by Morris water maze (MWM), along with oxidative stress and disturbance of central cholinergic system. However, administration of alpha-lipoic acid (50mg/kg, i.p.) for 28 days significantly restored cognitive deficits induced by BCCAO. Biochemical determination revealed that alpha-lipoic acid markedly decreased the production of malondialdehyde (MDA) and the generation of reactive oxidative species (ROS), and increased the level of reduced glutathione (GSH) in the hippocampal tissue. Additionally, alpha-lipoic acid raised the level of acetylcholine (ACh) and choline acetyltransferase (ChAT) and decreased the activity of acetycholinesterase (AChE) in the hippocampus. These results indicated that treatment with alpha-lipoic acid significantly improved behavioral alterations, protected against oxidative stress, and restored central cholinergic system in the rat model of vascular dementia induced by BCCAO.

摘要

慢性脑灌注不足引起的脑氧化应激被认为是血管性痴呆发病机制中的主要危险因素。在本研究中,我们研究了抗氧化剂α-硫辛酸对大鼠血管性痴呆的保护作用及其潜在机制。双侧颈总动脉闭塞(BCCAO)通过莫里斯水迷宫(MWM)测试诱发严重的认知缺陷,同时伴有氧化应激和中枢胆碱能系统紊乱。然而,腹腔注射α-硫辛酸(50mg/kg)28天可显著恢复BCCAO诱导的认知缺陷。生化测定显示,α-硫辛酸显著降低海马组织中丙二醛(MDA)的产生和活性氧(ROS)的生成,并提高还原型谷胱甘肽(GSH)水平。此外,α-硫辛酸提高了海马中乙酰胆碱(ACh)和胆碱乙酰转移酶(ChAT)的水平,并降低了乙酰胆碱酯酶(AChE)的活性。这些结果表明,α-硫辛酸治疗可显著改善行为改变,抵抗氧化应激,并恢复BCCAO诱导的血管性痴呆大鼠模型中的中枢胆碱能系统。

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