Raza Sana, Rajak Sangam, Yen Paul M, Sinha Rohit A
Department of Endocrinology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, 226014 India.
Laboratory of Hormonal Regulation, Cardiovascular and Metabolic Disorders Program, Duke-NUS Medical School, Singapore, 169857 Singapore.
NPJ Metab Health Dis. 2024;2(1):19. doi: 10.1038/s44324-024-00022-5. Epub 2024 Aug 2.
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.
代谢功能障碍相关脂肪性肝病(MASLD)源于肝脏脂质代谢的稳态失衡。患有MASLD的人肝脏中脂肪沉积增加,使他们更容易出现进一步的代谢紊乱,包括糖尿病、代谢功能障碍相关脂肪性肝炎(MASH)和其他终末期肝病。不幸的是,迄今为止,针对MASLD的药物治疗方法有限。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,使用自噬调节剂的临床前研究在解决MASLD及其向有害肝脏病理进展的缓解方面显示出有前景的结果。在这篇综述中,我们讨论了我们目前对自噬介导的肝脏脂质代谢的理解、其对MASLD治疗的治疗性调节,以及当前临床转化的局限性和范围。