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线粒体功能障碍作为代谢功能障碍相关脂肪性肝病的发病机制及治疗策略

Mitochondrial Dysfunction as a Pathogenesis and Therapeutic Strategy for Metabolic-Dysfunction-Associated Steatotic Liver Disease.

作者信息

Li Xiangqiong, Chen Wenling, Jia Zhuangzhuang, Xiao Yahui, Shi Anhua, Ma Xuan

机构信息

School of Basic Medical Sciences, Yunnan University of Chinese Medicine, Kunming 650500, China.

Yunnan Key Laboratory of Integrated Traditional Chinese and Western Medicine for Chronic Disease in Prevention and Treatment, Kunming 650500, China.

出版信息

Int J Mol Sci. 2025 Apr 30;26(9):4256. doi: 10.3390/ijms26094256.

Abstract

Metabolic-dysfunction-associated steatotic liver disease (MASLD) has emerged as a significant public health concern, attributed to its increasing prevalence and correlation with metabolic disorders, including obesity and type 2 diabetes. Recent research has highlighted that mitochondrial dysfunction can result in the accumulation of lipids in non-adipose tissues, as well as increased oxidative stress and inflammation. These factors are crucial in advancing the progression of MASLD. Despite advances in the understanding of MASLD pathophysiology, challenges remain in identifying effective therapeutic strategies targeting mitochondrial dysfunction. This review aims to consolidate current knowledge on how mitochondrial imbalance affects the development and progression of MASLD, while addressing existing research gaps and potential avenues for future research. This review was conducted after a systematic search of comprehensive academic databases such as PubMed, Embase, and Web of Science to gather information on mitochondrial dysfunction as well as mitochondrial-based treatments for MASLD.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)已成为一个重大的公共卫生问题,这归因于其患病率的不断上升以及与代谢紊乱(包括肥胖症和2型糖尿病)的相关性。最近的研究强调,线粒体功能障碍会导致非脂肪组织中脂质的积累,以及氧化应激和炎症的增加。这些因素在推进MASLD的进展中至关重要。尽管在理解MASLD病理生理学方面取得了进展,但在确定针对线粒体功能障碍的有效治疗策略方面仍存在挑战。本综述旨在整合当前关于线粒体失衡如何影响MASLD发展和进展的知识,同时解决现有研究差距以及未来研究的潜在途径。本综述是在对PubMed、Embase和Web of Science等综合学术数据库进行系统检索后进行的,以收集有关线粒体功能障碍以及MASLD基于线粒体的治疗方法的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b46/12072025/8a29d381a09a/ijms-26-04256-g002.jpg

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