Scoparone 可通过调节 PPARα 信号通路缓解非酒精性脂肪肝。

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
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引用次数: 0

摘要

Scoparone(Scop)是从茵陈蒿(Artemisia capillaris Thunb)中提取的一种天然化合物,已被证明具有改善非酒精性脂肪肝(NAFLD)的功效。本研究旨在探索其潜在机制。先用高脂饮食诱导 C57BL/6J 小鼠患上非酒精性脂肪肝,然后用 Scop 治疗 8 周。对肝组织进行 mRNA 测序以确定潜在靶点,并通过棕榈酸诱导的 AML12 肝细胞体外实验进行验证。mRNA 测序发现过氧化物酶体增殖激活受体α(PPARα)信号通路是 Scop 的靶点,体内和体外实验进一步证实了这一点。分子对接研究表明,Scop 可与人 PPARα 稳定结合。总之,Scop被证明能通过靶向PPARα信号通路缓解脂质代谢障碍和炎症,这为其在非酒精性脂肪肝治疗中的潜在应用提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scoparone alleviates nonalcoholic fatty liver disease by modulating the PPARα signaling pathway
Scoparone (Scop), a natural compound derived from Artemisia capillaris Thunb, has demonstrated efficacy in improving nonalcoholic fatty liver disease (NAFLD). This study aims to explore the underlying mechanism. NAFLD was induced by a high-fat diet in C57BL/6J mice, followed by an 8-week treatment with Scop. The effect of Scop on mice NAFLD was assessed. mRNA sequencing of liver tissues was performed to identify potential targets, which were validated through in vitro experiments using palmitic acid-induced AML12 hepatocytes. The results demonstrated that Scop promoted lipid metabolism, insulin sensitivity, and liver function, and alleviated inflammation in NAFLD mice. mRNA sequencing identified the peroxisome proliferator-activated receptor α (PPARα) signaling pathway as a target of Scop, which was further confirmed by in vivo and in vitro experiments. Molecular docking studies showed that Scop could bind stably to human PPARα. In summary, Scop was proven to alleviate lipid metabolism dysfunction and inflammation by targeting the PPARα signaling pathway, which provides a basis for its potential application in NAFLD treatment.
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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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