Yousef M Almoghrabi, Basmah M Eldakhakhny, Ghada Ajabnoor, Faisal Alandejani, Ahmad Jamal, Dareen Alyousfi, Ahmad M Alzahrani, Mostafa A Elsamanoudy, Taghreed Shamrani, Ayman Z Elsamanoudy
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引用次数: 0
Abstract
Insulin resistance (IR) is characterized by impaired insulin signaling in skeletal muscle, liver, and adipose tissue. Increasing evidence indicates mitochondrial dysfunction as a key factor contributing to IR. Mitochondrial resilience refers to the mitochondria's ability to adapt to metabolic stress by regulating biogenesis, dynamics, mitophagy, and redox homeostasis. Linking mitochondrial resilience with insulin signaling could be essential for maintaining metabolic health. This review aims to map and synthesize the existing literature on the relationship between mitochondrial resilience and insulin resistance, focusing on cellular and molecular mechanisms, tissue-specific roles, metabolic consequences, and translational evidence from both animal and human studies. This scoping review adhered to PRISMA-ScR guidelines and included comprehensive searches of PubMed, Scopus, Web of Science, Embase, and Google Scholar. It included experimental and observational studies, original articles, systematic reviews, and meta-analyses, while excluding non-English publications and animal studies without clinical relevance. A total of 7, 012 records were identified; after removing duplicates, screening, and assessing eligibility, 184 studies were included. The evidence shows that impaired mitochondrial biogenesis, defective mitochondrial dynamics, reduced mitophagy, and oxidative stress disturb insulin signaling and promote metabolic inflexibility. Conversely, enhancing mitochondrial resilience increases mitochondrial quantity and function. Lifestyle modification strategies and pharmacological intervention target these pathways to improve mitochondrial resilience. Importantly, understanding inter-individual differences in mitochondrial adaptive capacity may support the development of personalized therapeutic and nutritional strategies aimed at improving insulin sensitivity and metabolic outcomes. In conclusion, mitochondrial resilience provides a comprehensive framework connecting mitochondrial quality to insulin signaling and metabolic health. Focusing on mitochondrial resilience is a promising, mechanism-based strategy for preventing and managing insulin resistance and its related comorbidities.
胰岛素抵抗(IR)的特征是骨骼肌、肝脏和脂肪组织中的胰岛素信号受损。越来越多的证据表明,线粒体功能障碍是导致IR的关键因素。线粒体弹性是指线粒体通过调节生物发生、动力学、线粒体自噬和氧化还原稳态来适应代谢应激的能力。将线粒体弹性与胰岛素信号联系起来可能对维持代谢健康至关重要。这篇综述的目的是绘制和综合现有的关于线粒体弹性和胰岛素抵抗之间关系的文献,重点是细胞和分子机制,组织特异性作用,代谢后果,以及动物和人类研究的转化证据。该综述遵循PRISMA-ScR指南,包括PubMed、Scopus、Web of Science、Embase和谷歌Scholar的综合检索。它包括实验和观察性研究、原创文章、系统综述和荟萃分析,但不包括非英语出版物和没有临床相关性的动物研究。共确定了7012条记录;在剔除重复、筛选和评估合格性后,184项研究被纳入。有证据表明,线粒体生物发生受损、线粒体动力学缺陷、线粒体自噬减少和氧化应激干扰胰岛素信号传导并促进代谢不灵活性。相反,增强线粒体弹性可以增加线粒体的数量和功能。生活方式改变策略和药物干预针对这些途径,以提高线粒体的恢复能力。重要的是,了解线粒体适应能力的个体间差异可能有助于开发个性化的治疗和营养策略,以改善胰岛素敏感性和代谢结果。总之,线粒体弹性提供了一个将线粒体质量与胰岛素信号和代谢健康联系起来的综合框架。关注线粒体恢复力是预防和管理胰岛素抵抗及其相关合并症的一种有前途的、基于机制的策略。