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The renin angiotensin aldosterone system and insulin resistance in humans

机译:肾素血管紧张素醛固酮系统与人类胰岛素抵抗

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Alterations in the renin angiotensin aldosterone system (RAAS) contribute to the underlying pathophysiology of insulin resistance in humans; however, individual differences in the treatment response of insulin resistance to RAAS blockade persist. Thus, understanding inter-individual differences in the relationship between the RAAS and insulin resistance may provide insights into improved personalized treatments and improved outcomes. The effects of the systemic RAAS on blood pressure regulation and glucose metabolism have been studied extensively; however, recent discoveries on the influence of local tissue RAAS in the skeletal muscle, heart, vasculature, adipocytes, and pancreas have led to an improved understanding of how activated tissue RAAS influences the development of insulin resistance and diabetes in humans. Angiotensin II (ANGII) is the predominant RAAS component contributing to insulin resistance; however, other players such as aldosterone, renin, and ACE2 are also involved. This review examines the role of local ANGII activity on insulin resistance development in skeletal muscle, adipocytes, and pancreas, followed by a discussion of the other RAAS components implicated in insulin resistance, including ACE2, Ang1-7, renin, and aldosterone.
机译:肾素血管紧张素醛固酮系统(RAAS)的改变有助于人类胰岛素抵抗的潜在病理生理。但是,胰岛素抵抗RAAS阻滞的治疗反应仍存在个体差异。因此,了解RAAS与胰岛素抵抗之间关系的个体差异可能会为改进个性化治疗和改善结局提供真知灼见。已经广泛研究了全身性RAAS对血压调节和葡萄糖代谢的影响。然而,最近关于骨骼肌,心脏,脉管系统,脂肪细胞和胰腺中局部组织RAAS影响的发现,使人们对活化组织RAAS如何影响人类胰岛素抵抗和糖尿病的发展有了更好的了解。血管紧张素II(ANGII)是导致RAAS产生胰岛素抵抗的主要因素。但是,还涉及其他参与者,如醛固酮,肾素和ACE2。这篇综述检查了局部ANGII活性对骨骼肌,脂肪细胞和胰腺胰岛素抵抗发展的作用,然后讨论了与胰岛素抵抗有关的其他RAAS成分,包括ACE2,Ang1-7,肾素和醛固酮。

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