Li Weiwei, Huang Doudou, Luo Zichen, Zhou Ting, Jin Ziwen
School of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Pharmaceuticals (Basel). 2025 Jun 20;18(7):932. doi: 10.3390/ph18070932.
Yinchenhao decoction (YCHD), a classical herbal formula comprising , , and , has been clinically used for over 1000 years to treat cholestasis. However, its mechanism of action remains undefined. This study aimed to elucidate YCHD's therapeutic mechanisms against cholestasis, with a focus on the gut microbiota-mediated regulation of the farnesoid X receptor (FXR)-fibroblast growth factor 15 (FGF15) pathway. An alpha-naphthyl isothiocyanate (ANIT)-induced cholestasis mouse model was established. Mice received YCHD (3/9 g/kg) for 7 days. 16S rRNA sequencing, targeted LC/MS (bile acid (BA) quantification), untargeted GC/MS (fecal metabolite detection), qPCR/Western blot (FXR pathway analysis), fecal microbiota transplantation (FMT), and antibiotic depletion were employed to dissect the gut-liver axis interactions. YCHD alleviated cholestatic liver injury by reducing serum biomarkers, restoring BA homeostasis via FXR-FGF15 activation, and suppressing hepatic Cyp7a1-mediated BA synthesis. It remodeled gut microbiota, enriched FXR-activating secondary BAs (CDCA, DCA, CA), and restored the intestinal barrier integrity. Antibiotic cocktail abolished YCHD's efficacy, while FMT from YCHD-treated mice enhanced its therapeutic effects, confirming microbiota dependency. YCHD mitigates cholestasis through gut microbiota-driven FXR activation and direct hepatobiliary regulation. These findings bridge traditional medicine and modern pharmacology, highlighting microbiome modulation as a therapeutic strategy for cholestatic liver diseases.
茵陈蒿汤(YCHD)是一种由茵陈蒿、栀子和大黄组成的经典中药方剂,临床应用已逾千年,用于治疗胆汁淤积症。然而,其作用机制尚不清楚。本研究旨在阐明茵陈蒿汤治疗胆汁淤积症的作用机制,重点关注肠道微生物群介导的法尼酯X受体(FXR)-成纤维细胞生长因子15(FGF15)通路的调节。建立了α-萘异硫氰酸酯(ANIT)诱导的胆汁淤积小鼠模型。小鼠接受茵陈蒿汤(3/9 g/kg)治疗7天。采用16S rRNA测序、靶向液相色谱/质谱(胆汁酸(BA)定量)、非靶向气相色谱/质谱(粪便代谢物检测)、定量聚合酶链反应/蛋白质免疫印迹(FXR通路分析)、粪便微生物群移植(FMT)和抗生素清除来剖析肠-肝轴相互作用。茵陈蒿汤通过降低血清生物标志物、激活FXR-FGF15恢复BA稳态以及抑制肝脏Cyp7a1介导的BA合成来减轻胆汁淤积性肝损伤。它重塑了肠道微生物群,富集了激活FXR的次级BA(CDCA、DCA、CA),并恢复了肠道屏障完整性。抗生素鸡尾酒消除了茵陈蒿汤的疗效,而来自茵陈蒿汤治疗小鼠粪便微生物群移植增强了其治疗效果,证实了对微生物群的依赖性。茵陈蒿汤通过肠道微生物群驱动的FXR激活和直接肝胆调节减轻胆汁淤积。这些发现架起了传统医学与现代药理学之间的桥梁,突出了微生物群调节作为胆汁淤积性肝病治疗策略的重要性。