氧化炎症、线粒体功能障碍和脂肪毒性之间复杂的相互作用:关注它们在骨骼肌胰岛素抵抗发病机制中的作用以及膳食脂肪酸的调节作用

Angelina Passaro , Juana Maria Sanz , Nenad Naumovski , Domenico Sergi
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引用次数: 0

摘要

骨骼肌胰岛素抵抗是 2 型糖尿病(T2DM)发病机制中的关键因素。氧化性炎症,即炎症与氧化应激的共存和密切关系,以及线粒体功能障碍和脂肪毒性都与骨骼肌胰岛素抵抗的发病机制有关。最重要的是,这些胰岛素抵抗的效应因子能够相互促进,从而产生复杂的恶性循环。这篇综述旨在对氧化炎症、线粒体功能障碍和脂肪毒性之间密切的相互影响进行最新的批判性概述,它们是胰岛素抵抗的关键分子机制。此外,还将详细讨论膳食脂肪酸在调节这一恶性循环的关键参与者中的作用以及对骨骼肌胰岛素敏感性的影响。
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The complex interplay between oxinflammation, mitochondrial dysfunction and lipotoxicity: Focus on their role in the pathogenesis of skeletal muscle insulin resistance and modulation by dietary fatty acids

Skeletal muscle insulin resistance is pivotal in the pathogenesis of type 2 diabetes mellitus (T2DM). Oxinflammation, referred to as the coexistence of and tight relationship between inflammation and oxidative stress, along with mitochondrial dysfunction and lipotoxicity have all been implicated in the pathogenesis of skeletal muscle insulin resistance. Most importantly, these effectors of insulin resistance are able to fuel one another, thereby generating a complex vicious cycle. This review aims at providing an updated and critical overview on the intimate cross-talk between oxinflammation, mitochondrial dysfunction and lipotoxicity as key molecular mechanisms underpinning insulin resistance. Additionally, the role of dietary fatty acids in modulating the key actors of this vicious cycle and the repercussions on skeletal muscle insulin sensitivity will be discussed in detail.

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CiteScore
2.60
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0.00%
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审稿时长
46 days
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