Beijing Key Laboratory of Innovative Drug Discovery of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193, China.
Key Laboratory of Bioactive Substances and Resource Utilization of Chinese Herbal Medicine, Ministry of Education, Beijing 100193, China.
Int J Mol Sci. 2019 Jul 25;20(15):3633. doi: 10.3390/ijms20153633.
Currently, hundreds of herbal products with potential hepatotoxicity were available in the literature. A comprehensive summary and analysis focused on these potential hepatotoxic herbal products may assist in understanding herb-induced liver injury (HILI). In this work, we collected 335 hepatotoxic medicinal plants, 296 hepatotoxic ingredients, and 584 hepatoprotective ingredients through a systematic literature retrieval. Then we analyzed these data from the perspectives of phylogenetic relationship and structure-toxicity relationship. Phylogenetic analysis indicated that hepatotoxic medicinal plants tended to have a closer taxonomic relationship. By investigating the structures of the hepatotoxic ingredients, we found that alkaloids and terpenoids were the two major groups of hepatotoxicity. We also identified eight major skeletons of hepatotoxicity and reviewed their hepatotoxic mechanisms. Additionally, 15 structural alerts (SAs) for hepatotoxicity were identified based on SARpy software. These SAs will help to estimate the hepatotoxic risk of ingredients from herbs. Finally, a herb-ingredient network was constructed by integrating multiple datasets, which will assist to identify the hepatotoxic ingredients of herb/herb-formula quickly. In summary, a systemic analysis focused on HILI was conducted which will not only assist to identify the toxic molecular basis of hepatotoxic herbs but also contribute to decipher the mechanisms of HILI.
目前,文献中已有数百种具有潜在肝毒性的草药产品。对这些潜在肝毒性草药产品进行全面总结和分析,可能有助于了解草药引起的肝损伤(HILI)。在这项工作中,我们通过系统文献检索收集了 335 种肝毒性药用植物、296 种肝毒性成分和 584 种肝保护成分。然后,我们从系统发育关系和结构-毒性关系的角度分析了这些数据。系统发育分析表明,肝毒性药用植物往往具有更密切的分类学关系。通过研究肝毒性成分的结构,我们发现生物碱和萜类化合物是肝毒性的两个主要类别。我们还确定了 8 种主要的肝毒性骨架,并回顾了它们的肝毒性机制。此外,基于 SARpy 软件,我们确定了 15 个肝毒性结构警示(SA)。这些 SA 将有助于估计草药成分的肝毒性风险。最后,通过整合多个数据集构建了一个草药-成分网络,这将有助于快速识别草药/草药配方的肝毒性成分。总之,我们对 HILI 进行了系统分析,这不仅有助于确定肝毒性草药的毒性分子基础,还有助于阐明 HILI 的机制。