葛根素通过抑制交感神经流出诱导的脂肪分解缓解酒精性肝病。

IF 5.5
Ke Zheng, Liu Yang, Rui-Shuo Zhang, Yi-Han Qian, Yu-Ge Zhou, Wei-Fan Huang, Jia-Cheng Lin, Yan-Jun Shi, Xiao-Ni Kong
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引用次数: 0

摘要

本研究旨在评价葛根素(PUE)对酒精性肝病(ALD)的治疗效果,并从脂肪分解和肝脂肪变性的角度探讨其可能的作用机制。采用血清生化指标及苏木精和伊红(H&E)染色对肝脏和脂肪组织进行组织学检查,评估PUE对ALD的疗效。采用Western blotting (WB)分析和免疫荧光(IHC)染色研究PUE改善ALD的潜在机制。我们证明PUE通过减轻乙醇诱导的肝损伤和脂质积累,抑制脂质合成基因的表达,上调脂质代谢基因的表达,以及通过抑制脂肪甘油三酯脂肪酶(ATGL)的激活和激素敏感脂肪酶(HSL)的磷酸化来减少脂肪分解,从而减轻ALD中的脂肪变性。综上所述,PUE通过抑制交感神经外流介导的关键脂解酶ATGL和HSL的激活来改善ALD。这些发现为PUE在ALD临床治疗中的潜在应用提供了坚实的理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Puerarin Alleviates Alcoholic Liver Disease via Suppressing Lipolysis Induced by Sympathetic Outflow.

The aim of this study was to evaluate the therapeutic effect of puerarin (PUE) on alcoholic liver disease (ALD) and elucidate the potential mechanism from the perspective of lipolysis and hepatic steatosis. Assessment of PUE efficacy against ALD was performed using serum biochemical parameters and the histological examination of liver and adipose tissue via Hematoxylin and eosin (H&E) staining. The potential mechanisms underlying the amelioration of ALD by PUE were investigated using Western blotting (WB) analysis and immunofluorescence (IHC) staining. We demonstrated that PUE attenuated steatosis in ALD by alleviating ethanol-induced liver damage and lipid accumulation, suppressing the expression of lipid synthesis genes, upregulating the expression of lipid metabolism genes, and reducing lipolysis by inhibiting adipose triglyceride lipase (ATGL) activation and the phosphorylation of hormone-sensitive lipase (HSL). In conclusion, PUE ameliorates ALD by inhibiting the sympathetic outflow-mediated activation of key lipolysis enzymes ATGL and HSL. These findings provide a solid theoretical foundation for the potential application of PUE in the clinical treatment of ALD.

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