Autolysosomal Dysfunction in Obesity-induced Metabolic Inflammation and Related Disorders.

IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Lenny Yi Tong Cheong, Eka Norfaishanty Saipuljumri, Gavin Wen Zhao Loi, Jialiu Zeng, Chih Hung Lo
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Abstract

Purpose of review: Obesity is a global health crisis affecting individuals across all age groups, significantly increasing the risk of metabolic disorders such as type 2 diabetes (T2D), metabolic dysfunction-associated fatty liver disease (MAFLD), and cardiovascular diseases. The World Health Organization reported in 2022 that 2.5 billion adults were overweight, with 890 million classified as obese, emphasizing the urgent need for effective interventions. A critical aspect of obesity's pathophysiology is meta-inflammation-a chronic, systemic low-grade inflammatory state driven by excess adipose tissue, which disrupts metabolic homeostasis. This review examines the role of autolysosomal dysfunction in obesity-related metabolic disorders, exploring its impact across multiple metabolic organs and evaluating potential therapeutic strategies that target autophagy and lysosomal function.

Recent findings: Emerging research highlights the importance of autophagy in maintaining cellular homeostasis and metabolic balance. Obesity-induced lysosomal dysfunction impairs the autophagic degradation process, contributing to the accumulation of damaged organelles and toxic aggregates, exacerbating insulin resistance, lipotoxicity, and chronic inflammation. Studies have identified autophagic defects in key metabolic tissues, including adipose tissue, skeletal muscle, liver, pancreas, kidney, heart, and brain, linking autophagy dysregulation to the progression of metabolic diseases. Preclinical investigations suggest that pharmacological and nutritional interventions-such as AMPK activation, caloric restriction mimetics, and lysosomal-targeting compounds-can restore autophagic function and improve metabolic outcomes in obesity models. Autolysosomal dysfunction is a pivotal contributor to obesity-associated metabolic disorders , influencing systemic inflammation and metabolic dysfunction. Restoring autophagy and lysosomal function holds promise as a therapeutic strategy to mitigate obesity-driven pathologies. Future research should focus on translating these findings into clinical applications, optimizing targeted interventions to improve metabolic health and reduce obesity-associated complications.

肥胖引起的代谢性炎症及相关疾病的自溶酶体功能障碍。
综述目的:肥胖是影响所有年龄组个体的全球性健康危机,显著增加代谢性疾病的风险,如2型糖尿病(T2D)、代谢功能障碍相关脂肪性肝病(MAFLD)和心血管疾病。世界卫生组织在2022年报告称,有25亿成年人超重,其中8.9亿人被列为肥胖,强调迫切需要采取有效干预措施。肥胖病理生理学的一个关键方面是炎症-一种由过量脂肪组织驱动的慢性、全身性低级别炎症状态,它破坏了代谢稳态。本文综述了自噬酶体功能障碍在肥胖相关代谢疾病中的作用,探讨了其在多个代谢器官中的影响,并评估了针对自噬和溶酶体功能的潜在治疗策略。最新发现:新兴研究强调了自噬在维持细胞稳态和代谢平衡中的重要性。肥胖诱导的溶酶体功能障碍会损害自噬降解过程,导致受损细胞器和毒性聚集体的积累,加剧胰岛素抵抗、脂肪毒性和慢性炎症。研究已经确定了关键代谢组织中的自噬缺陷,包括脂肪组织、骨骼肌、肝脏、胰腺、肾脏、心脏和大脑,将自噬失调与代谢性疾病的进展联系起来。临床前研究表明,药物和营养干预-如AMPK激活,热量限制模拟物和溶酶体靶向化合物-可以恢复肥胖模型的自噬功能并改善代谢结果。自溶酶体功能障碍是肥胖相关代谢障碍的关键因素,影响全身炎症和代谢功能障碍。恢复自噬和溶酶体功能有望作为减轻肥胖驱动病理的治疗策略。未来的研究应侧重于将这些发现转化为临床应用,优化有针对性的干预措施,以改善代谢健康,减少肥胖相关并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Obesity Reports
Current Obesity Reports Medicine-General Medicine
CiteScore
16.40
自引率
1.10%
发文量
25
期刊介绍: The main objective of Current Obesity Reports is to provide expert review articles on recent advancements in the interdisciplinary field of obesity research. Our aim is to offer clear, insightful, and balanced contributions that will benefit all individuals involved in the treatment and prevention of obesity, as well as related conditions such as cardiovascular diseases, endocrine disorders, gynecological issues, cancer, mental health, respiratory complications, and rheumatological diseases. We strive to redefine the way knowledge is expressed and provide organized content for the benefit of our readership.
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