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线粒体功能障碍与胰岛素抵抗相关心脏病的相关性。

Relevance of mitochondrial dysfunction in heart disease associated with insulin resistance conditions.

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

Pflugers Arch. 2022 Jan;474(1):21-31. doi: 10.1007/s00424-021-02638-8. Epub 2021 Nov 22.

Abstract

Insulin resistance plays a key role in the development and progression of obesity, diabetes, and their complications. Moreover, insulin resistance is considered the principal link between metabolic diseases and cardiovascular diseases. Heart disease associated with insulin resistance is one of the most important consequences of both obesity and diabetes, and it is characterized by impaired cardiac energetics, diastolic dysfunction, and finally heart failure. Mitochondrion plays a key role in cell energy homeostasis and is the main source of reactive oxygen species. Obesity and diabetes are associated with alterations in mitochondrial function and dynamics. Mitochondrial dysfunction is characterized by changes in mitochondrial respiratory chain with reduced ATP production and elevated reactive oxygen species production. These mitochondrial alterations together with inflammation contribute to the development and progression of heart disease under insulin resistance conditions. Finally, numerous miRNAs participate in the regulation of energy substrate metabolism, reactive oxygen species production, and apoptotic pathways within the mitochondria. This notion supports the relevance of interactions between miRNAs and mitochondrial dysfunction in the pathophysiology of metabolic heart disease.

摘要

胰岛素抵抗在肥胖、糖尿病及其并发症的发生和发展中起着关键作用。此外,胰岛素抵抗被认为是代谢性疾病和心血管疾病之间的主要联系。与胰岛素抵抗相关的心脏病是肥胖和糖尿病的最重要后果之一,其特征是心脏能量代谢受损、舒张功能障碍,最终导致心力衰竭。线粒体在细胞能量稳态中起着关键作用,是活性氧的主要来源。肥胖和糖尿病与线粒体功能和动力学的改变有关。线粒体功能障碍的特征是线粒体呼吸链改变,导致 ATP 生成减少和活性氧生成增加。这些线粒体改变与炎症一起,导致胰岛素抵抗状态下心脏病的发生和发展。最后,许多 miRNA 参与调节线粒体中的能量底物代谢、活性氧生成和凋亡途径。这一观点支持 miRNA 与线粒体功能障碍在代谢性心脏病病理生理学中的相互作用的相关性。

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