自噬和肝脏脂质代谢:对 MASLD 的机理认识和治疗潜力。

Sana Raza, Sangam Rajak, Paul M. Yen, Rohit A. Sinha
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摘要

代谢功能障碍相关性脂肪性肝病(MASLD)源于肝脏脂质代谢的平衡失调。代谢功能障碍相关性脂肪性肝病患者肝脏中脂肪沉积增加,易导致进一步的代谢紊乱,包括糖尿病、代谢功能障碍相关性脂肪性肝炎(MASH)和其他终末期肝病。遗憾的是,迄今为止,针对 MASLD 的药物疗法十分有限。自噬是一种细胞分解代谢过程,已成为哺乳动物肝细胞脂质代谢的主要机制。此外,使用自噬调节剂进行的临床前研究显示,自噬调节剂在缓解MASLD和减轻其发展为有害肝脏病变方面具有良好的效果。在这篇综述中,我们将讨论我们目前对自噬介导的肝脏脂质代谢的理解、自噬对治疗 MASLD 的调节作用以及目前的局限性和临床转化的范围。
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Autophagy and hepatic lipid metabolism: mechanistic insight and therapeutic potential for MASLD
Metabolic dysfunction-associated steatotic liver disease (MASLD) originates from a homeostatic imbalance in hepatic lipid metabolism. Increased fat deposition in the liver of people suffering from MASLD predisposes them to develop further metabolic derangements, including diabetes mellitus, metabolic dysfunction-associated steatohepatitis (MASH), and other end-stage liver diseases. Unfortunately, only limited pharmacological therapies exist for MASLD to date. Autophagy, a cellular catabolic process, has emerged as a primary mechanism of lipid metabolism in mammalian hepatocytes. Furthermore, preclinical studies with autophagy modulators have shown promising results in resolving MASLD and mitigating its progress into deleterious liver pathologies. In this review, we discuss our current understanding of autophagy-mediated hepatic lipid metabolism, its therapeutic modulation for MASLD treatment, and current limitations and scope for clinical translation.
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