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肾脏中的肾素-血管紧张素系统:有哪些新进展?

Renin-angiotensin system in the kidney: What is new?

作者信息

Ferrão Fernanda M, Lara Lucienne S, Lowe Jennifer

机构信息

Fernanda M Ferrão, Jennifer Lowe, Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.

出版信息

World J Nephrol. 2014 Aug 6;3(3):64-76. doi: 10.5527/wjn.v3.i3.64.

Abstract

The renin-angiotensin system (RAS) has been known for more than a century as a cascade that regulates body fluid balance and blood pressure. Angiotensin II(Ang II) has many functions in different tissues; however it is on the kidney that this peptide exerts its main functions. New enzymes, alternative routes for Ang IIformation or even active Ang II-derived peptides have now been described acting on Ang II AT1 or AT2 receptors, or in receptors which have recently been cloned, such as Mas and AT4. Another interesting observation was that old members of the RAS, such as angiotensin converting enzyme (ACE), renin and prorenin, well known by its enzymatic activity, can also activate intracellular signaling pathways, acting as an outside-in signal transduction molecule or on the renin/(Pro)renin receptor. Moreover, the endocrine RAS, now is also known to have paracrine, autocrine and intracrine action on different tissues, expressing necessary components for local Ang II formation. This in situ formation, especially in the kidney, increases Ang II levels to regulate blood pressure and renal functions. These discoveries, such as the ACE2/Ang-(1-7)/Mas axis and its antangonistic effect rather than classical deleterious Ang II effects, improves the development of new drugs for treating hypertension and cardiovascular diseases.

摘要

肾素-血管紧张素系统(RAS)作为调节体液平衡和血压的级联反应,已为人所知达一个多世纪之久。血管紧张素II(Ang II)在不同组织中具有多种功能;然而,这种肽的主要功能是在肾脏发挥的。现在已经描述了新的酶、Ang II形成的替代途径,甚至是源自活性Ang II的肽,它们作用于Ang II的AT1或AT2受体,或作用于最近克隆的受体,如Mas和AT4。另一个有趣的发现是,RAS的一些旧成员,如血管紧张素转换酶(ACE)、肾素和前肾素,因其酶活性而广为人知,它们也可以激活细胞内信号通路,作为一种由外向内的信号转导分子或作用于肾素/(原)肾素受体。此外,现在还已知内分泌RAS对不同组织具有旁分泌、自分泌和胞内分泌作用,表达局部Ang II形成所需的成分。这种原位形成,尤其是在肾脏中,会增加Ang II水平以调节血压和肾功能。这些发现,如ACE2/Ang-(1-7)/Mas轴及其拮抗作用而非经典的有害Ang II作用,促进了治疗高血压和心血管疾病新药的开发。

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