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全球代谢组学和靶向代谢组学研究表明,柴胡毒素(一种有毒的聚乙炔类物质)通过抑制小鼠体内的GABA受体诱导脑部损伤。

Global and targeted metabolomics reveal that Bupleurotoxin, a toxic type of polyacetylene, induces cerebral lesion by inhibiting GABA receptor in mice.

作者信息

Zhang Zhongxiao, Lu Cheng, Liu Xinru, Su Juan, Dai Weixing, Yan Shikai, Lu Aiping, Zhang Weidong

机构信息

School of Pharmacy, Second Military Medical University , Shanghai 200433, PR China.

出版信息

J Proteome Res. 2014 Feb 7;13(2):925-33. doi: 10.1021/pr400968c. Epub 2013 Dec 23.

Abstract

Polyacetylenes are widely distributed in food plants and medicinal herbs, which have been shown to have highly neurotoxic effects. However, there were insufficient studies on the toxicity of these compounds. Thus, a series of experiments was designed to elucidate the toxicity mechanism of bupleurotoxin (BETX) as a representative polyacetylene. First, male BALB/c mice were intragastrically administered 2.5 mg/kg of bodyweight BETX once a day for seven consecutive days. The histopathological results showed that BETX could induce severe morphological damages in the brain hippocampus. We then used metabolomics approaches to screen serum samples from the control and BETX-treated groups. The global metabolomics results revealed 17 metabolites that were perturbed after BETX treatment. Four of these metabolites were then verified by targeted metabolomics. Bioinformatics analysis with the Ingenuity Pathway Analysis (IPA) software found a strong correlation between the GABA receptor signaling pathway and these metabolites. On the basis of these results, a validation test using a rat hippocampal neuron cell line was performed, and the results confirmed that BETX inhibited GABA-induced currents (IGABA) in a competitive manner. In summary, our study illustrated the molecular mechanism of the toxicity of polyacetylenes. In addition, our study was instructive for the study of other toxic medical herbs.

摘要

聚乙炔广泛分布于食用植物和药草中,已被证明具有高度的神经毒性作用。然而,关于这些化合物毒性的研究并不充分。因此,设计了一系列实验来阐明作为代表性聚乙炔的柴胡毒素(BETX)的毒性机制。首先,雄性BALB/c小鼠连续7天每天经口给予体重2.5mg/kg的BETX。组织病理学结果表明,BETX可诱导脑海马区严重的形态学损伤。然后,我们使用代谢组学方法筛选对照组和BETX处理组的血清样本。整体代谢组学结果显示,BETX处理后有17种代谢物发生了扰动。其中4种代谢物随后通过靶向代谢组学进行了验证。使用Ingenuity Pathway Analysis(IPA)软件进行的生物信息学分析发现,GABA受体信号通路与这些代谢物之间存在强相关性。基于这些结果,使用大鼠海马神经元细胞系进行了验证试验,结果证实BETX以竞争性方式抑制GABA诱导的电流(IGABA)。总之,我们的研究阐明了聚乙炔毒性的分子机制。此外,我们的研究对其他有毒药草的研究具有指导意义。

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