Chiglitazar 通过调节小鼠体内的多种途径减轻高脂饮食诱发的非酒精性脂肪肝。

IF 3.8 3区 医学 Q2 CELL BIOLOGY Molecular and Cellular Endocrinology Pub Date : 2024-08-02 DOI:10.1016/j.mce.2024.112337
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引用次数: 0

摘要

非酒精性脂肪性肝病(NAFLD)是全球最常见的慢性肝病之一,但目前仍缺乏有效的非酒精性脂肪性肝病干预策略。本研究旨在探讨泛 PPAR 激动剂 chiglitazar 对小鼠非酒精性脂肪肝的保护功效及其潜在的分子机制。雄性 C57BL/6J 小鼠连续 8 周摄入高脂饮食(HFD)以产生非酒精性脂肪肝,然后在没有或有 5 mg/kg/d 或 10 mg/kg/d chiglitazar 灌胃的情况下继续摄入高脂饮食 10 周。奇格列扎显著改善了非酒精性脂肪肝小鼠的血脂异常和胰岛素抵抗,改善了肝脏脂肪变性,减轻了肝脏炎症和氧化应激。RNA-seq发现,吉格列氮通过多种途径,包括脂肪酸代谢调节、胰岛素信号通路和AMPK信号通路,缓解了HFD诱导的小鼠非酒精性脂肪肝。这项研究证明了吉格列扎对非酒精性脂肪肝的潜在治疗作用。吉格列嗪通过调节多种途径改善非酒精性脂肪肝。
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Chiglitazar attenuates high-fat diet-induced nonalcoholic fatty liver disease by modulating multiple pathways in mice

Nonalcoholic fatty liver disease (NAFLD) is one of the most common chronic liver diseases worldwide; however, effective intervention strategies for NAFLD are still unavailable. The present study sought to investigate the efficacy of chiglitazar, a pan-PPAR agonist, in protecting against NAFLD in mice and its underlying molecular mechanism. Male C57BL/6 J mice were fed a high-fat diet (HFD) for 8 weeks to generate NAFLD and the HFD was continued for an additional 10 weeks in the absence or presence of 5 mg/kg/d or 10 mg/kg/d chiglitazar by gavage. Chiglitazar significantly improved dyslipidemia and insulin resistance, ameliorated hepatic steatosis and reduced liver inflammation and oxidative stress in NAFLD mice. RNA-seq revealed that chiglitazar alleviated HFD-induced NAFLD in mice through multiple pathways, including fatty acid metabolism regulation, insulin signaling pathway, and AMPK signaling pathway. This study demonstrated the potential therapeutic effect of chiglitazar on NAFLD. Chiglitazar ameliorated NAFLD by modulating multiple pathways.

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来源期刊
Molecular and Cellular Endocrinology
Molecular and Cellular Endocrinology 医学-内分泌学与代谢
CiteScore
9.00
自引率
2.40%
发文量
174
审稿时长
42 days
期刊介绍: Molecular and Cellular Endocrinology was established in 1974 to meet the demand for integrated publication on all aspects related to the genetic and biochemical effects, synthesis and secretions of extracellular signals (hormones, neurotransmitters, etc.) and to the understanding of cellular regulatory mechanisms involved in hormonal control.
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