Department of Pharmacology, School of Pharmacy, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai, 201203, China.
Key Laboratory of Liver and Kidney Diseases (Ministry of Education), Institute of Liver Diseases, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, 528 Zhangheng Road, Shanghai, 201204, China.
J Ethnopharmacol. 2021 Mar 1;267:113544. doi: 10.1016/j.jep.2020.113544. Epub 2020 Nov 2.
ETHNOPHARMACOLOGICAL RELEVANCE: Gut microbiome dysbiosis is closely associated with cholestatic liver disease. Huangqi decoction (HQD), a traditional herbal formula, has protection against cholestatic liver injury. However, the effect of HQD on gut microbiome remains unknown. AIM OF THE STUDY: To investigate the effect of HQD on 3, 5-diethoxycarbonyl-1, 4-dihydrocollidine (DDC) induced cholestatic liver injury and its effect on the gut microbiome profiles. MATERIALS AND METHODS: Mice with DDC-induced cholestatic liver injury were treated with low and high doses of HQD for 8 weeks. Fecal samples were analyzed by 16 S ribosomal DNA sequencing. Barrier function as well as intestinal and hepatic inflammation was analyzed by real-time PCR and western blotting. RESULTS: HQD treatment ameliorated the DDC-induced liver injury and collagen deposition around hepatic bile ducts. Moreover, decreased diversity, reduced richness, and abnormal composition of intestinal microbiota of cholestatic mice were remarkably attenuated by HQD supplementation. Differences in bacterial abundance, including levels of Prevotellaceae_NK3B31_group, Alistipes, and Gordonibacter, were increased in DDC-induced mice, as compared with control mice, and were decreased after HQD treatment. Moreover, intestinal dysbiosis promoted disruption of the intestinal barrier in cholestatic mice. However, HQD treatment alleviated intestinal barrier dysfunction. Importantly, increased hepatic expression of pro-inflammatory factors and the NLRP3 inflammasome, which have a positive correlation with differential bacteria, were characteristics found in DDC-induced cholestatic mice that were alleviated upon treatment with HQD. CONCLUSION: HQD treatment alleviated gut microbiota dysbiosis, ameliorated the intestinal barrier dysfunction, inhibited liver inflammation, and protected against DDC-induced cholestatic liver injury.
民族药理学相关性:肠道微生物群落失调与胆汁淤积性肝病密切相关。黄芪汤(HQD)是一种传统的草药配方,对胆汁淤积性肝损伤具有保护作用。然而,HQD 对肠道微生物群落的影响尚不清楚。 研究目的:研究 HQD 对 3,5-二乙氧羰基-1,4-二氢吡啶(DDC)诱导的胆汁淤积性肝损伤的作用及其对肠道微生物群落谱的影响。 材料和方法:用 DDC 诱导的胆汁淤积性肝损伤小鼠给予 HQD 低、高剂量治疗 8 周。通过 16S 核糖体 DNA 测序分析粪便样本。实时 PCR 和 Western blot 分析屏障功能以及肠道和肝脏炎症。 结果:HQD 治疗改善了 DDC 诱导的肝损伤和肝内胆管周围胶原沉积。此外,HQD 补充显著减弱了胆汁淤积小鼠肠道微生物群落的多样性降低、丰富度降低和组成异常。与对照组相比,DDC 诱导的小鼠肠道中细菌丰度的差异增加,包括普雷沃氏菌科 NK3B31 群、拟杆菌属和戈登氏菌属的水平,HQD 治疗后降低。此外,肠道失调促进了胆汁淤积小鼠肠道屏障的破坏。然而,HQD 治疗缓解了肠道屏障功能障碍。重要的是,增加的肝内促炎因子和 NLRP3 炎性体的表达,与差异细菌呈正相关,是 DDC 诱导的胆汁淤积性肝损伤小鼠的特征,用 HQD 治疗后得到缓解。 结论:HQD 治疗缓解了肠道微生物群落失调,改善了肠道屏障功能障碍,抑制了肝炎症,并防止了 DDC 诱导的胆汁淤积性肝损伤。
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