秦连红曲煎剂调节FXR/TGR5/GLP-1通路改善非酒精性脂肪肝小鼠胰岛素抵抗的生物信息学和实验研究

IF 3.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY ACS Omega Pub Date : 2024-11-03 eCollection Date: 2024-11-12 DOI:10.1021/acsomega.4c07463
Zhongyi Zhang, Yunliang He, Mei Zhao, Xin He, Zubing Zhou, Yuanyuan Yue, Tao Shen, Juncheng Liu, Gan Zhang, Yong Zhang
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引用次数: 0

摘要

背景:青莲红曲水煎剂(QLHQD)是一种传统中药,在缓解与非酒精性脂肪肝(NAFLD)相关的代谢问题方面具有潜力。然而,其确切的作用模式仍不确定。研究目的本研究旨在评估 QLHQD 治疗非酒精性脂肪肝的疗效和机制。研究方法本研究利用非酒精性脂肪肝小鼠模型评估 QLHQD 对脂质代谢(包括血脂和肝脂肪变性)以及糖代谢(包括血糖水平、OGTT 结果和血清胰岛素)的影响。研究人员利用网络药理学、生物信息学和分子对接来探索 QLHQD 如何改善非酒精性脂肪肝的治疗。通过WB和免疫组化验证了参与这些机制的关键蛋白。此外,还检测了下游通路靶点的表达,以进一步验证 QLHQD 改善非酒精性脂肪肝的胰岛素抵抗机制。结果:动物实验表明,QLHQD可减轻非酒精性脂肪肝小鼠的血脂异常、肝脏脂肪变性、血糖水平、胰岛素抵抗指数和OGTT结果(P < 0.05或0.01)。网络药理学和生物信息学分析表明,QLHQD对非酒精性脂肪肝的影响可能涉及胆汁酸分泌途径。随后通过 Western 印迹、免疫组化和 qPCR 验证表明,QLHQD 可通过 FXR/TGR5/GLP-1 信号通路影响 NAFLD 小鼠的脂肪代谢和胰岛素敏感性。结论QLHQD能明显缓解高脂饮食诱导的非酒精性脂肪肝小鼠模型的糖脂代谢紊乱。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。
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Qinlian Hongqu Decoction Modulates FXR/TGR5/GLP-1 Pathway to Improve Insulin Resistance in NAFLD Mice: Bioinformatics and Experimental Study.

Background: 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. Objective: This study aims to evaluate the efficacy and mechanisms of QLHQD in treating NAFLD. Methods: 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. Results: Animal studies demonstrated that QLHQD alleviated lipid abnormalities, hepatic steatosis, blood glucose levels, the insulin resistance index, and the OGTT results in NAFLD mice (P < 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. Conclusion: 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.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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