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改善黄芪甲苷对大鼠慢性脑灌注不足后学习记忆障碍的影响。

Ameliorating the effect of astragaloside IV on learning and memory deficit after chronic cerebral hypoperfusion in rats.

作者信息

Kim Sooyong, Kang Il-Hwan, Nam Jung-Bum, Cho Yoonchul, Chung Doo-Young, Kim Seung-Hwan, Kim Jeong-Soo, Cho Yong-Deok, Hong Eun-Ki, Sohn Nak-Won, Shin Jung-Won

机构信息

Department of East-West Medical Science, Graduate School of East-West Medical Science, Kyung Hee University, Yongin 446-701, Korea.

出版信息

Molecules. 2015 Jan 23;20(2):1904-21. doi: 10.3390/molecules20021904.

Abstract

Astragaloside IV (AS-IV) has been reported to have a prominent antioxidant effect and was proposed as a promising agent for the prevention of neurodegenerative disorders accompanied by cognitive impairment. The present study investigated the ameliorating effect of AS-IV on learning and memory deficits induced by chronic cerebral hypoperfusion in rats. Rats were treated with two doses of AS-IV (10 and 20 mg/kg, i.p.) daily for 28 days starting from the 5th week after permanent bilateral common carotid artery occlusion. AS-IV treatment (at dose of 20 mg/kg) significantly improved the spatial learning and memory deficits assessed using the Morris water maze test in rats with chronic cerebral hypoperfusion. AS-IV significantly attenuated neuronal apoptosis as well as the levels of superoxide dismutase and lipid peroxidation markers, including malondialdehyde and 4-hydroxy-2-nonenal, in the hippocampus. AS-IV also significantly reduced 8-hydroxy-2'-deoxyguanosine expression, a maker of oxidative DNA damage, while significantly inhibited the astrocyte and microglia activation in the hippocampus. The results indicate that AS-IV has therapeutic potential for the prevention of dementia caused by cerebral hypoperfusion and suggest that the ameliorating effect of AS-IV on learning and memory deficits might be the result of suppressing neuronal apoptosis and oxidative damage in the hippocampus.

摘要

黄芪甲苷IV(AS-IV)已被报道具有显著的抗氧化作用,并被认为是预防伴有认知障碍的神经退行性疾病的一种有前景的药物。本研究调查了AS-IV对大鼠慢性脑灌注不足诱导的学习和记忆缺陷的改善作用。从永久性双侧颈总动脉闭塞后第5周开始,大鼠每天接受两剂量的AS-IV(10和20mg/kg,腹腔注射),持续28天。AS-IV治疗(20mg/kg剂量)显著改善了慢性脑灌注不足大鼠使用莫里斯水迷宫试验评估的空间学习和记忆缺陷。AS-IV显著减轻了海马体中的神经元凋亡以及超氧化物歧化酶水平和脂质过氧化标志物水平,包括丙二醛和4-羟基-2-壬烯醛。AS-IV还显著降低了氧化DNA损伤标志物8-羟基-2'-脱氧鸟苷的表达,同时显著抑制了海马体中的星形胶质细胞和小胶质细胞激活。结果表明,AS-IV对预防脑灌注不足引起的痴呆具有治疗潜力,并表明AS-IV对学习和记忆缺陷的改善作用可能是抑制海马体中神经元凋亡和氧化损伤的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803e/6272750/bcfab0ce0f55/molecules-20-01904-g001.jpg

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