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脂肪组织中的替代性肾素-血管紧张素系统途径及其在肥胖发病机制中的作用。

Alternative renin-angiotensin system pathways in adipose tissue and their role in the pathogenesis of obesity.

作者信息

Slamkova M, Zorad S, Krskova K

出版信息

Endocr Regul. 2016 Oct 1;50(4):229-240. doi: 10.1515/enr-2016-0025.

Abstract

Adipose tissue expresses all the renin-angiotensin system (RAS) components that play an important role in the adipogenesis, lipid and glucose metabolism regulation in an auto/paracrine manner. The classical RAS has been found to be over-activated during the adipose tissue enlargement, thus elevated generation of angiotensin II (Ang II) may contribute to the obesity pathogenesis. The contemporary view on the RAS has become more complex with the discovery of alternative pathways, including angiotensin-converting enzyme 2 (ACE2)/angiotensin (Ang)-(1-7)/Mas receptor, (pro)renin receptor, as well as angiotensin IV(Ang IV)/AT4 receptor. Ang-(1-7) via Mas receptor counteracts with most of the deleterious effects of the Ang II-mediated by AT1 receptor implying its beneficial role in the glucose and lipid metabolism, oxidative stress, inflammation, and insulin resistance. Pro(renin) receptor may play a role (at least partial) in the pathogenesis of the obesity by increasing the local production of Ang II in adipose tissue as well as triggering signal transduction independently of Ang II. In this review, modulation of alternative RAS pathways in adipose tissue during obesity is discussed and the involvement of Ang-(1-7), (pro)renin and AT4 receptors in the regulation of adipose tissue homeostasis and insulin resistance is summarized.

摘要

脂肪组织表达所有肾素 - 血管紧张素系统(RAS)的组分,这些组分以自分泌/旁分泌方式在脂肪生成、脂质和葡萄糖代谢调节中发挥重要作用。已发现经典RAS在脂肪组织增大过程中过度激活,因此血管紧张素II(Ang II)生成增加可能促成肥胖症的发病机制。随着替代途径的发现,包括血管紧张素转换酶2(ACE2)/血管紧张素(Ang) - (1 - 7)/ Mas受体、(前)肾素受体以及血管紧张素IV(Ang IV)/ AT4受体,当代对RAS的观点变得更加复杂。Ang - (1 - 7)通过Mas受体抵消了由AT1受体介导的Ang II的大多数有害作用,这意味着其在葡萄糖和脂质代谢、氧化应激、炎症和胰岛素抵抗中具有有益作用。(前)肾素受体可能通过增加脂肪组织中Ang II的局部产生以及独立于Ang II触发信号转导在肥胖症发病机制中发挥作用(至少部分作用)。在本综述中,讨论了肥胖期间脂肪组织中替代RAS途径的调节,并总结了Ang - (1 - 7)、(前)肾素和AT4受体在脂肪组织稳态和胰岛素抵抗调节中的作用。

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