National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Chem Biol Interact. 2023 Dec 1;386:110774. doi: 10.1016/j.cbi.2023.110774. Epub 2023 Oct 20.
Reports on Chinese patent medicines preparations containing Epimedii Folium (EF) and Psoraleae Fructus (PF) resulting in idiosyncratic drug-induced liver injury (IDILI) have received widespread attention. Previous studies have shown that bavachin and epimedin B-two active ingredients derived from both EF and PF-are potential components associated with IDILI, but the underlying mechanism remains unclear. We evaluated bavachin and epimedin B-induced IDILI under TNF-α-mediated immunological stress conditions and generated liver lipid metabolism profiles using lipidomics and multivariate statistical analysis. We next applied transcriptomics to identify the differential gene expression on the transcription level. Our results showed that co-exposure to bavachin, epimedin B under immunological stress conditions resulted in obvious liver injury. The differential metabolites screened in our study were closely related to the immune homeostasis of the liver. Sixteen differentially expressed genes were found, Zc3h6 and R3hdml were upregulated, while Sumo2, Cd74, Banp, Oas3, Oas2, Gbp8, Slfn8, Gbp2b, Serpina3g, Zbtb40, H2-Ab1, Osgin1, Tgtp1 and Hspa1b were all downregulated. These differentially expressed genes were associated with biological processes concerning metabolic process and immune system process. Further integrative analysis indicated that bavachin combined with epimedin B affected genes that were not only related to immune system processes, but also to lipid metabolism. Ultimately, this led to an imbalance in the immune microenvironment in the liver and may have contributed to the observed liver injury.
有关含有淫羊藿(EF)和补骨脂(PF)的中药制剂引起的特发性药物性肝损伤(IDILI)的报告受到了广泛关注。先前的研究表明,二氢黄酮醇和淫羊藿苷 B-两种源自 EF 和 PF 的活性成分-可能是与 IDILI 相关的潜在成分,但潜在机制尚不清楚。我们在 TNF-α介导的免疫应激条件下评估了二氢黄酮醇和淫羊藿苷 B 诱导的 IDILI,并使用脂质组学和多变量统计分析生成了肝脂质代谢谱。接下来,我们应用转录组学在转录水平上识别差异基因表达。我们的结果表明,在免疫应激条件下共同暴露于二氢黄酮醇和淫羊藿苷 B 会导致明显的肝损伤。我们筛选的差异代谢物与肝脏的免疫稳态密切相关。发现了 16 个差异表达基因,其中 Zc3h6 和 R3hdml 上调,而 Sumo2、Cd74、Banp、Oas3、Oas2、Gbp8、Slfn8、Gbp2b、Serpina3g、Zbtb40、H2-Ab1、Osgin1、Tgtp1 和 Hspa1b 下调。这些差异表达基因与代谢过程和免疫系统过程等生物学过程有关。进一步的综合分析表明,二氢黄酮醇与淫羊藿苷 B 结合影响的基因不仅与免疫系统过程有关,还与脂质代谢有关。最终,这导致肝脏免疫微环境失衡,可能导致观察到的肝损伤。