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脂毒性驱动的代谢功能障碍相关脂肪性肝病(MASLD)。

Lipotoxicity-driven metabolic dysfunction-associated steatotic liver disease (MASLD).

作者信息

Iturbe-Rey Santiago, Maccali Claudia, Arrese Marco, Aspichueta Patricia, Oliveira Claudia P, Castro Rui E, Lapitz Ainhoa, Izquierdo-Sanchez Laura, Bujanda Luis, Perugorria Maria J, Banales Jesus M, Rodrigues Pedro M

机构信息

Department of Liver and Gastrointestinal Diseases, Biogipuzkoa Health Research Institute, Donostia University Hospital, University of the Basque Country (UPV/EHU), Donostia-San Sebastian, Spain.

Clinical and Experimental Gastroenterology Laboratory LIM-07, Department of Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

出版信息

Atherosclerosis. 2025 Jan;400:119053. doi: 10.1016/j.atherosclerosis.2024.119053. Epub 2024 Nov 14.

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) encompasses a spectrum of liver lesions, ranging from simple steatosis to metabolic dysfunction-associated steatohepatitis (MASH), that may further progress to cirrhosis. MASLD is estimated to affect more than one third of the general population and it represents a risk factor for end-stage liver failure and liver cancer, substantially contributing to liver-related morbidity and mortality. Although the pathogenesis of MASLD is incompletely understood, it is known to consist of a multifactorial process influenced by extrinsic and intrinsic factors such as metabolic, environmental and demographic features, gut microbiota and genetics. Dysregulation of both extracellular and intracellular lipid composition is known to promote the generation of toxic lipid species, thereby triggering lipotoxicity and cellular stress. These events ultimately lead to the activation of distinct cell death pathways, resulting in inflammation, fibrogenesis and, eventually, carcinogenesis. In this manuscript, we provide a comprehensive review of the role of lipotoxicity during MASLD pathogenesis, discussing the most relevant lipid species and related molecular mechanisms, summarizing the cell type-specific effects and highlighting the most promising putative therapeutic strategies for modulating lipotoxicity and lipid metabolism in MASLD.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)涵盖了一系列肝脏病变,从单纯性脂肪变性到代谢功能障碍相关脂肪性肝炎(MASH),后者可能进一步发展为肝硬化。据估计,MASLD影响超过三分之一的普通人群,是终末期肝衰竭和肝癌的危险因素,对肝脏相关的发病率和死亡率有重大影响。尽管MASLD的发病机制尚未完全明确,但已知它是一个受外在和内在因素影响的多因素过程,这些因素包括代谢、环境和人口统计学特征、肠道微生物群和遗传学。细胞外和细胞内脂质组成的失调已知会促进有毒脂质种类的产生,从而引发脂毒性和细胞应激。这些事件最终导致不同细胞死亡途径的激活,进而引发炎症、纤维化,最终导致癌变。在本手稿中,我们全面综述了脂毒性在MASLD发病机制中的作用,讨论了最相关的脂质种类和相关分子机制,总结了细胞类型特异性效应,并强调了调节MASLD中脂毒性和脂质代谢最有前景的潜在治疗策略。

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