Zhang Zhongyi, He Yunliang, Zhao Mei, He Xin, Zhou Zubing, Yue Yuanyuan, Shen Tao, Liu Juncheng, Zhang Gan, Zhang Yong
Institute of Traditional Chinese Medicine, Sichuan Academy of Chinese Medicine Sciences, Chengdu 610041, China.
School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
ACS Omega. 2024 Nov 3;9(45):45447-45466. doi: 10.1021/acsomega.4c07463. eCollection 2024 Nov 12.
Qinglian Hongqu decoction (QLHQD), a traditional Chinese herbal remedy, shows potential in alleviating metabolic issues related to nonalcoholic fatty liver disease (NAFLD). However, its precise mode of action remains uncertain. This study aims to evaluate the efficacy and mechanisms of QLHQD in treating NAFLD. This study utilized a NAFLD mouse model to assess the effects of QLHQD on lipid metabolism, including blood lipids and hepatic steatosis, as well as glucose metabolism, including blood glucose levels, OGTT results, and serum insulin. Network pharmacology, bioinformatics, and molecular docking were used to explore how QLHQD may improve NAFLD treatment. Key proteins involved in these mechanisms were validated via WB and immunohistochemistry. Additionally, the expression of downstream pathway targets was examined to further validate the insulin resistance mechanism by which QLHQD improves NAFLD. Animal studies demonstrated that QLHQD alleviated lipid abnormalities, hepatic steatosis, blood glucose levels, the insulin resistance index, and the OGTT results in NAFLD mice ( < 0.05 or 0.01). Network pharmacology and bioinformatics analyses indicated that the effects of QLHQD on NAFLD might involve bile acid secretion pathways. Subsequent validation through Western blotting, immunohistochemistry, and qPCR demonstrated that QLHQD may influence fat metabolism and insulin sensitivity in NAFLD mice via the FXR/TGR5/GLP-1 signaling pathway. QLHQD significantly alleviates glucose and lipid metabolism disorders in a high-fat diet-induced NAFLD mouse model. Its mechanism of action may involve the activation of the FXR/TGR5/GLP-1 signaling pathway in the gut, which reduces lipid accumulation and insulin resistance.
清莲红曲汤(QLHQD)是一种传统中药方剂,在缓解与非酒精性脂肪性肝病(NAFLD)相关的代谢问题方面显示出潜力。然而,其确切作用机制仍不确定。本研究旨在评估QLHQD治疗NAFLD的疗效和机制。本研究利用NAFLD小鼠模型评估QLHQD对脂质代谢(包括血脂和肝脂肪变性)以及葡萄糖代谢(包括血糖水平、口服葡萄糖耐量试验(OGTT)结果和血清胰岛素)的影响。采用网络药理学、生物信息学和分子对接技术来探索QLHQD如何改善NAFLD的治疗。通过蛋白质免疫印迹法(WB)和免疫组织化学法验证了这些机制中涉及的关键蛋白。此外,检测下游通路靶点的表达以进一步验证QLHQD改善NAFLD的胰岛素抵抗机制。动物研究表明,QLHQD可减轻NAFLD小鼠的脂质异常、肝脂肪变性、血糖水平、胰岛素抵抗指数和OGTT结果(<0.05或0.01)。网络药理学和生物信息学分析表明,QLHQD对NAFLD的作用可能涉及胆汁酸分泌途径。随后通过蛋白质免疫印迹法、免疫组织化学法和定量聚合酶链反应(qPCR)验证表明,QLHQD可能通过法尼醇X受体(FXR)/G蛋白偶联胆汁酸受体5(TGR5)/胰高血糖素样肽-1(GLP-1)信号通路影响NAFLD小鼠的脂肪代谢和胰岛素敏感性。QLHQD可显著减轻高脂饮食诱导的NAFLD小鼠模型中的葡萄糖和脂质代谢紊乱。其作用机制可能涉及激活肠道中的FXR/TGR5/GLP-1信号通路,从而减少脂质积累和胰岛素抵抗。