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预先给予灵芝孢子对大鼠海马的神经保护作用。

Neuroprotective effect of preadministration with Ganoderma lucidum spore on rat hippocampus.

作者信息

Zhou Yan, Qu Ze-qiang, Zeng Yuan-shan, Lin Yu-kun, Li Yan, Chung Peter, Wong Ricky, Hägg Urban

机构信息

Department of Histology and Embryology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.

出版信息

Exp Toxicol Pathol. 2012 Nov;64(7-8):673-80. doi: 10.1016/j.etp.2010.12.011. Epub 2011 Jan 15.

Abstract

The aim of this study was to investigate if preadministration with Ganoderma lucidum spore (GLS) could (1) alleviate oxidative stress and mitochondrial dysfunction in rat hippocampus of intracerebroventricular (ICV) injection of streptozotocin (STZ), (2) protect neurons from apoptosis, and (3) improve cognitive dysfunction. Three groups of Sprague-Dawley rats were preadministrated with GLS at doses of 2.0, 4.0 and 8.0 g/kg, respectively, for 3 weeks before the ICV STZ injury. Thereafter the rats were operated with ICV STZ (1.5 mg/kg) bilaterally on days 1 and 3. The behavioral alterations, oxidative stress indexes, ATP, cytochrome oxidase (CytOx), and histopathology of hippocampal neurons were studied. The results showed that ICV STZ model rats exhibited a significant increase of malondialdehyde (MDA), a significant decrease of glutathione reductase (GR), reduced glutathione (GSH), ATP and CytOx, accompanied with marked impairments in spatial learning and memory, and severe damage of hippocampal neuron. In conclusion, preadministration with GLS at dose of 8.0 g/kg in ICV STZ rats significantly reversed these abnormalities. In conclusion, preadministration with GLS might protect hippocampus from oxidative impairment and energy metabolism disturbance of ICV STZ. This may also provide useful information for future research on the pathogenesis and prevention of Alzheimer's disease (AD).

摘要

本研究旨在探讨预先给予灵芝孢子(GLS)是否能够:(1)减轻脑室内注射链脲佐菌素(STZ)的大鼠海马中的氧化应激和线粒体功能障碍;(2)保护神经元免于凋亡;以及(3)改善认知功能障碍。将三组Sprague-Dawley大鼠分别以2.0、4.0和8.0 g/kg的剂量预先给予GLS,持续3周,然后进行脑室内STZ损伤。之后,在第1天和第3天对大鼠双侧进行脑室内注射STZ(1.5 mg/kg)。研究了行为改变、氧化应激指标、ATP、细胞色素氧化酶(CytOx)以及海马神经元的组织病理学。结果显示,脑室内注射STZ的模型大鼠丙二醛(MDA)显著增加,谷胱甘肽还原酶(GR)、还原型谷胱甘肽(GSH)、ATP和CytOx显著降低,同时伴有空间学习和记忆的明显受损以及海马神经元的严重损伤。总之,预先给予8.0 g/kg剂量的GLS可显著逆转脑室内注射STZ大鼠的这些异常。总之,预先给予GLS可能保护海马免受脑室内注射STZ所致的氧化损伤和能量代谢紊乱。这也可能为未来关于阿尔茨海默病(AD)发病机制和预防的研究提供有用信息。

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