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苯甲酰乌头原碱的药理作用、分子机制及药代动力学:一项系统综述

Pharmacological effects, molecular mechanisms, and pharmacokinetics of benzoylaconine: a systematic review.

作者信息

Zhuang Huamei, Yao Hong

机构信息

School of Pharmacy and Medical technology, Putian University, Putian, China.

Key Laboratory of Pharmaceutical Analysis and Laboratory Medicine, Putian University, Putian, China.

出版信息

Front Pharmacol. 2025 Aug 5;16:1571153. doi: 10.3389/fphar.2025.1571153. eCollection 2025.

Abstract

Benzoylaconine (BAC), a key active metabolite in traditional Chinese medicine, is derived from the subsoil roots of Fuzi ( Debx [Ranunculaceae, Debx roots]). BAC has garnered considerable research attention because of its therapeutic effects against cardiovascular disease, inflammation, and arthritis, and this has led to continual updates in the literature. This systematic review summarizes evidence on the pharmacological effects, molecular mechanisms, and pharmacokinetics of BAC. PubMed and Web of Science were searched for relevant articles published between January 2000 and November 2024. Genes, proteins, and pathways related to the activity and therapeutic effects of BAC were identified. BAC usually targets proteins such as ACE2, IL-6, MAPK, PI3K, Akt, STAT3, TNF-α, and VEGF. The identified genes and proteins were subjected to protein-protein interaction analysis, molecular docking between BAC and protein hubs, and bioinformatic analyses (gene ontology, Kyoto Encyclopedia of Genes and Genomes, and disease ontology analyses). Protein-protein interaction analysis and molecular docking indicated IL-6, Akt1, and STAT3 as key targets of BAC. These findings offer theoretical insights into the potential therapeutic mechanisms of BAC and may inform its future development as a pharmacological agent.

摘要

苯甲酰乌头原碱(BAC)是中药中的一种关键活性代谢产物,源自附子(毛茛科植物乌头子根)的地下根。由于BAC对心血管疾病、炎症和关节炎具有治疗作用,因此受到了大量研究关注,这也使得相关文献不断更新。本系统综述总结了BAC的药理作用、分子机制和药代动力学方面的证据。通过检索PubMed和Web of Science数据库,查找2000年1月至2024年11月期间发表的相关文章。确定了与BAC活性和治疗作用相关的基因、蛋白质和信号通路。BAC通常作用于如ACE2、IL - 6、MAPK、PI3K、Akt、STAT3、TNF - α和VEGF等蛋白质。对所鉴定的基因和蛋白质进行了蛋白质 - 蛋白质相互作用分析、BAC与蛋白质枢纽的分子对接以及生物信息学分析(基因本体论、京都基因与基因组百科全书和疾病本体论分析)。蛋白质 - 蛋白质相互作用分析和分子对接表明IL - 6、Akt1和STAT3是BAC的关键靶点。这些发现为BAC的潜在治疗机制提供了理论见解,并可能为其作为一种药物的未来发展提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c9c/12392121/694e398a0350/fphar-16-1571153-g001.jpg

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