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紫萁贯众提取物的体内外神经保护作用。

Neuroprotective effects of a Coeloglossum viride var. Bracteatum extract in vitro and in vivo.

机构信息

Center on Translational Neuroscience, College of Life & Environmental Science, Minzu University of China, Beijing, 100081, China.

State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.

出版信息

Sci Rep. 2017 Aug 23;7(1):9209. doi: 10.1038/s41598-017-08957-0.

Abstract

The excessive release and accumulation of glutamate in the brain is known to be associated with excitotoxicity. CE, an extract derived from the plant Coeloglossum viride var. Bracteatum, exerted neuroprotective effects against amyloid toxicity and oxidative stress in cortical neurons. The aims of this study are to examine whether CE also attenuates glutamate neurotoxicity in rat primary cultured cortical neurons and to determine the effect of CE in vivo. According to the results of MTT, LDH release, and TUNEL assays, the CE treatment significantly reduced glutamate-induced neurotoxicity in a dose-dependent manner. Moreover, the protective effects of CE were blocked by an Akt inhibitor, LY294002, suggesting that the PI3K/Akt signalling pathway is involved in the neuroprotective effects of CE. In addition, CE might regulate the PKC-GluA2 axis to prevent neuronal apoptosis. CE also protected against dopaminergic neuronal loss in a mouse model of MPTP-induced PD. Based on our results, CE exerted neuroprotective effects both in vitro and in vivo, thus providing a potential therapeutic target for the treatment or prevention of neurodegeneration.

摘要

已知大脑中谷氨酸的过度释放和积累与兴奋性毒性有关。CE 是从 Coeloglossum viride var. Bracteatum 植物中提取的一种物质,对皮质神经元的淀粉样毒性和氧化应激具有神经保护作用。本研究旨在探讨 CE 是否也能减轻原代培养大鼠皮质神经元中的谷氨酸神经毒性,并确定 CE 在体内的作用。根据 MTT、LDH 释放和 TUNEL 检测结果,CE 处理以剂量依赖的方式显著减轻了谷氨酸诱导的神经毒性。此外,CE 的保护作用被 Akt 抑制剂 LY294002 阻断,表明 PI3K/Akt 信号通路参与了 CE 的神经保护作用。此外,CE 可能通过调节 PKC-GluA2 轴来防止神经元凋亡。CE 还可以防止 MPTP 诱导的 PD 小鼠模型中多巴胺能神经元的丢失。基于我们的结果,CE 既在体外又在体内发挥了神经保护作用,因此为治疗或预防神经退行性变提供了一个潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a42/5569100/e9c8686406d1/41598_2017_8957_Fig1_HTML.jpg

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