S-烯丙基半胱氨酸可减轻链脲佐菌素诱导的阿尔茨海默病实验性痴呆小鼠模型中与氧化应激相关的认知障碍和神经退行性变。

S-allyl cysteine attenuates oxidative stress associated cognitive impairment and neurodegeneration in mouse model of streptozotocin-induced experimental dementia of Alzheimer's type.

机构信息

Neurotoxicology laboratory, Department of Medical Elementology and Toxicology (Fund for the Improvement of Science and Technology sponsored by DST and Special Assistance Programme sponsored by UGC), Jamia Hamdard (Hamdard University), Hamdard Nagar, New Delhi-110062, India.

出版信息

Brain Res. 2011 May 10;1389:133-42. doi: 10.1016/j.brainres.2011.02.072. Epub 2011 Mar 1.

Abstract

S-allyl cysteine (SAC), a sulfur containing amino acid derived from garlic, has been reported to have antioxidant, anti-cancer, antihepatotoxic and neurotrophic activity. This study was designed to examine the pre-treatment effects of SAC on cognitive deficits and oxidative damage in the hippocampus of intracerebroventricular streptozotocin (ICV-STZ)-infused mice. Mice pre-treated with SAC (30mg/kg) and vehicle (intraperitoneal; once daily for 15days) were bilaterally injected with ICV-STZ (2.57mg/kg body weight), whereas sham rats received the same volume of vehicle. The pre-treatment of this drug to Swiss albino mice has prevented the cognitive and neurobehavioral impairments. An increased latency and path length were observed in lesion, i.e. streptozotocin (STZ) group as compared to sham group and these were protected significantly in STZ group pre-treated with SAC. Levels of reduced glutathione (GSH) and its dependent enzymes (Glutathione peroxidase [GPx] and glutathione reductase [GR]) were decreased in STZ group as compared to sham group and pre-treatment of STZ group with SAC has protected their activities significantly. Conversely, the elevated level of thiobarbituric acid reactive substances (TBARS) in STZ group was attenuated significantly in SAC pre-treated group when compared with STZ lesioned group. Apoptotic parameters like DNA fragmentation, expression of Bcl2 and p53 were protected by the pre-treatment of SAC against STZ induced cognitive impairment. This study concludes that intervention of SAC could prevent free radicals associated deterioration of cognitive functions and neurobehavioral activities.

摘要

S-烯丙基半胱氨酸(SAC)是一种从大蒜中提取的含硫氨基酸,具有抗氧化、抗癌、抗肝毒性和神经营养活性。本研究旨在探讨 SAC 预处理对脑室注射链脲佐菌素(ICV-STZ)诱导的小鼠海马认知功能障碍和氧化损伤的影响。SAC(30mg/kg)和载体(腹腔内;每日一次,共 15 天)预处理的小鼠双侧脑室注射 ICV-STZ(2.57mg/kg 体重),而假手术大鼠则接受相同体积的载体。该药物对瑞士白化小鼠的预处理可预防认知和神经行为障碍。与假手术组相比,损伤组(即链脲佐菌素(STZ)组)观察到潜伏期和路径长度增加,而 SAC 预处理的 STZ 组则显著保护。与假手术组相比,STZ 组的还原型谷胱甘肽(GSH)及其依赖酶(谷胱甘肽过氧化物酶[GPx]和谷胱甘肽还原酶[GR])水平降低,SAC 预处理的 STZ 组的这些酶活性显著保护。相反,与 STZ 损伤组相比,SAC 预处理组 STZ 组的硫代巴比妥酸反应物质(TBARS)水平显著降低。SAC 预处理可防止 DNA 片段化、Bcl2 和 p53 表达等凋亡参数,从而防止 SAC 预处理引起的认知障碍。本研究得出结论,SAC 的干预可以防止与自由基相关的认知功能和神经行为活动的恶化。

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