Regulation of obesity and insulin resistance by hypoxia-inducible factors

J. Ban, Robin J. Ruthenborg, Kevin w Cho, Jung-whan Kim
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引用次数: 42

Abstract

In obesity, dysregulated metabolism and aberrant expansion of adipose tissue lead to the development of tissue hypoxia that plays an important role in contributing to obesity-associated metabolic disorders. Recent studies utilizing adipocyte-specific hypoxia-inducible factor-α (HIF-α) gain- or loss-of-function animal models highlight the pivotal involvement of hypoxic responses in the pathogenesis of obesity-associated inflammation and insulin resistance. HIF-1α, a master transcription factor of oxygen homeostasis, induces inflammation and insulin resistance in obesity, whereas its isoform, HIF-2α, exerts opposing functions in these obesity-associated metabolic phenotypes. In this review, recent evidence elucidating functional implications of adipocyte HIFs in obesity and, more importantly, how these regulate obesity-associated inflammation, fibrosis, and insulin resistance will be discussed. Further, we propose that modulation of HIF-1 could be a potential novel therapeutic strategy for antidiabetic treatment.
低氧诱导因子对肥胖和胰岛素抵抗的调节
在肥胖中,代谢失调和脂肪组织的异常扩张导致组织缺氧的发展,这在肥胖相关的代谢紊乱中起着重要作用。最近利用脂肪细胞特异性缺氧诱导因子-α (HIF-α)获得或丧失功能的动物模型的研究强调了缺氧反应在肥胖相关炎症和胰岛素抵抗的发病机制中的关键作用。HIF-1α是一种主要的氧稳态转录因子,在肥胖中诱导炎症和胰岛素抵抗,而其同型异构体HIF-2α在这些肥胖相关的代谢表型中发挥相反的功能。在这篇综述中,最近的证据阐明脂肪细胞hif在肥胖中的功能意义,更重要的是,这些如何调节肥胖相关的炎症、纤维化和胰岛素抵抗将被讨论。此外,我们提出调节HIF-1可能是一种潜在的抗糖尿病治疗新策略。
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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