Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Curr Hypertens Rep. 2013 Feb;15(1):59-70. doi: 10.1007/s11906-012-0323-2.
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.
肾素-血管紧张素-醛固酮系统(RAAS)的改变导致了人类胰岛素抵抗的潜在病理生理学变化;然而,胰岛素抵抗对 RAAS 阻断的治疗反应存在个体差异。因此,了解 RAAS 和胰岛素抵抗之间的个体差异关系可能为改善个体化治疗和改善预后提供思路。RAAS 对血压调节和葡萄糖代谢的影响已经得到了广泛的研究;然而,最近关于局部组织 RAAS 在骨骼肌、心脏、血管、脂肪细胞和胰腺中的影响的发现,使人们更好地理解了激活的组织 RAAS 如何影响人类胰岛素抵抗和糖尿病的发展。血管紧张素 II(ANGII)是导致胰岛素抵抗的主要 RAAS 成分;然而,其他如醛固酮、肾素和 ACE2 等也参与其中。这篇综述探讨了局部 ANGII 活性在骨骼肌、脂肪细胞和胰腺中对胰岛素抵抗发展的作用,随后讨论了其他与胰岛素抵抗相关的 RAAS 成分,包括 ACE2、Ang1-7、肾素和醛固酮。