Department of Cardiology, State Key Laboratory of Transvascular Implantation Devices, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Translational Medicine Center, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Lipids Health Dis. 2024 Apr 22;23(1):117. doi: 10.1186/s12944-024-02108-x.
Metabolic dysfunction-associated steatotic liver disease (MASLD) has garnered considerable attention globally. Changing lifestyles, over-nutrition, and physical inactivity have promoted its development. MASLD is typically accompanied by obesity and is strongly linked to metabolic syndromes. Given that MASLD prevalence is on the rise, there is an urgent need to elucidate its pathogenesis. Hepatic lipid accumulation generally triggers lipotoxicity and induces MASLD or progress to metabolic dysfunction-associated steatohepatitis (MASH) by mediating endoplasmic reticulum stress, oxidative stress, organelle dysfunction, and ferroptosis. Recently, significant attention has been directed towards exploring the role of gut microbial dysbiosis in the development of MASLD, offering a novel therapeutic target for MASLD. Considering that there are no recognized pharmacological therapies due to the diversity of mechanisms involved in MASLD and the difficulty associated with undertaking clinical trials, potential targets in MASLD remain elusive. Thus, this article aimed to summarize and evaluate the prominent roles of lipotoxicity, ferroptosis, and gut microbes in the development of MASLD and the mechanisms underlying their effects. Furthermore, existing advances and challenges in the treatment of MASLD were outlined.
代谢相关脂肪性肝病(MAFLD)已引起全球广泛关注。生活方式改变、营养过剩和体力活动不足促进了其发展。MAFLD 通常伴有肥胖症,与代谢综合征密切相关。鉴于 MAFLD 的患病率呈上升趋势,迫切需要阐明其发病机制。肝内脂质蓄积通常会引发脂毒性,并通过介导内质网应激、氧化应激、细胞器功能障碍和铁死亡,诱导 MAFLD 或进展为代谢相关脂肪性肝炎(MASH)。最近,人们越来越关注肠道微生物失调在 MAFLD 发展中的作用,为 MAFLD 提供了一个新的治疗靶点。由于 MAFLD 涉及的机制多样性以及临床试验的难度,目前尚无公认的药物治疗方法,因此,MAFLD 的潜在靶点仍难以确定。因此,本文旨在总结和评估脂毒性、铁死亡和肠道微生物在 MAFLD 发展中的突出作用及其影响的机制,并概述 MAFLD 治疗的现有进展和挑战。