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运用网络药理学和分子对接技术探索附子所致神经毒性的机制。

Exploring the mechanisms of neurotoxicity caused by fuzi using network pharmacology and molecular docking.

作者信息

An Junsha, Fan Huali, Han Mingyu, Peng Cheng, Xie Jie, Peng Fu

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, China.

State Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2022 Aug 30;13:961012. doi: 10.3389/fphar.2022.961012. eCollection 2022.

Abstract

Safety has always been an important issue affecting the development of traditional Chinese medicine industry, especially for toxic medicinal materials, the establishment of risk prevention and control measures for toxic herbs is of great significance to improving the use of traditional Chinese medicine in clinical. Fuzi is a kind of traditional Chinese medicine and its toxicity has become the most important obstacle of limit in clinical using. In this paper, network pharmacology and molecular docking technology were used to analyze the main toxic components of Fuzi, the key targets and the mechanism of neurotoxicity. We carried out CCK-8 and WB assays, and detected LDH release and SDH activity. It was verified that aconitine caused neurotoxicity through a variety of pathways, including MAPK signaling pathway, pathways related to Akt protein, destruction of cell membrane integrity, damage of mitochondrial function affecting energy metabolism and apoptosis. What's more, this study confirmed that aconitine could produce neurotoxicity by promoting apoptosis of hippocampus neuron and decreasing its quantity through Nissl Staining and TUNEL assay. This paper found and confirmed multiple targets and various pathways causing neurotoxicity of Fuzi, in order to provide reference for clinical application and related research.

摘要

安全性一直是影响中药产业发展的重要问题,尤其是对于有毒中药材而言,建立有毒中药材的风险防控措施对提高中药临床应用水平具有重要意义。附子是一种中药,其毒性已成为临床应用受限的最重要障碍。本文采用网络药理学和分子对接技术分析附子的主要毒性成分、关键靶点及神经毒性机制。我们进行了CCK-8和WB实验,并检测了LDH释放和SDH活性。结果证实乌头碱通过多种途径导致神经毒性,包括MAPK信号通路、与Akt蛋白相关的途径、破坏细胞膜完整性、损害线粒体功能影响能量代谢以及诱导凋亡。此外,本研究通过尼氏染色和TUNEL检测证实乌头碱可通过促进海马神经元凋亡并减少其数量而产生神经毒性。本文发现并证实了导致附子神经毒性的多个靶点和多种途径,为临床应用及相关研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/053c/9468872/5cc1f6b1cf24/fphar-13-961012-g001.jpg

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