Martin Sheree D, McGee Sean L
Metabolic Remodelling Laboratory, Metabolic Research Unit, School of Medicine, Deakin University, Waurn Ponds 3217, Australia.
Metabolic Remodelling Laboratory, Metabolic Research Unit, School of Medicine, Deakin University, Waurn Ponds 3217, Australia.
Biochim Biophys Acta. 2014 Apr;1840(4):1303-12. doi: 10.1016/j.bbagen.2013.09.019. Epub 2013 Sep 20.
The prevalence of type 2 diabetes is rapidly increasing world-wide and insulin resistance is central to the aetiology of this disease. The biology underpinning the development of insulin resistance is not completely understood and the role of impaired mitochondrial function in the development of insulin resistance is controversial.
This review will provide an overview of the major processes regulated by mitochondria, before examining the evidence that has investigated the relationship between mitochondrial function and insulin action. Further considerations aimed at clarifying some controversies surrounding this issue will also be proposed.
Controversy on this issue is fuelled by our lack of understanding of some of the basic biological interactions between mitochondria and insulin regulated processes in the context of insults thought to induce insulin resistance. Aspects that have not yet been considered are tissue/cell type specific responses, mitochondrial responses to site-specific impairments in mitochondrial function and as yet uncharacterised retrograde signalling from mitochondria.
Further investigation of the relationship between mitochondria and insulin action could reveal novel mechanisms contributing to insulin resistance in specific patient subsets. This article is part of a Special Issue entitled Frontiers of Mitochondrial Research.
2型糖尿病在全球的患病率正在迅速上升,胰岛素抵抗是该疾病病因的核心。胰岛素抵抗发生发展的生物学机制尚未完全明确,线粒体功能受损在胰岛素抵抗发生中的作用也存在争议。
本综述将概述线粒体调控的主要过程,然后审视研究线粒体功能与胰岛素作用之间关系的证据。还将提出旨在阐明围绕该问题的一些争议的进一步思考。
在被认为可诱导胰岛素抵抗的损伤背景下,我们对线粒体与胰岛素调控过程之间的一些基本生物学相互作用缺乏了解,这加剧了该问题上的争议。尚未考虑的方面包括组织/细胞类型特异性反应、线粒体对线粒体功能位点特异性损伤的反应以及尚未明确的线粒体逆行信号传导。
进一步研究线粒体与胰岛素作用之间的关系可能揭示特定患者亚群中导致胰岛素抵抗的新机制。本文是名为《线粒体研究前沿》的特刊的一部分。