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本文引用的文献

1
Triple-combination treatment with olmesartan medoxomil/amlodipine/ hydrochlorothiazide in Hispanic/Latino patients with hypertension: the TRINITY study.奥美沙坦酯/氨氯地平/氢氯噻嗪三联治疗高血压的西班牙裔/拉丁裔患者:TRINITY 研究。
Ethn Dis. 2014 Winter;24(1):41-7.
2
ANG-(3-4) inhibits renal Na+-ATPase in hypertensive rats through a mechanism that involves dissociation of ANG II receptors, heterodimers, and PKA.血管紧张素(3-4) 通过一种涉及血管紧张素 II 受体、异二聚体和 PKA 解离的机制抑制高血压大鼠的肾钠-ATP 酶。
Am J Physiol Renal Physiol. 2014 Apr 15;306(8):F855-63. doi: 10.1152/ajprenal.00488.2013. Epub 2014 Feb 12.
3
New frontiers in the intrarenal Renin-Angiotensin system: a critical review of classical and new paradigms.肾脏内肾素-血管紧张素系统的新前沿:对经典和新范例的批判性回顾。
Front Endocrinol (Lausanne). 2013 Nov 11;4:166. doi: 10.3389/fendo.2013.00166. eCollection 2013.
4
Dose-dependent effects of angiotensin-(1-7) on the NHE3 exchanger and [Ca(2+)](i) in in vivo proximal tubules.血管紧张素-(1-7)对体内近端小管 NHE3 交换器和 [Ca(2+)](i)的剂量依赖性作用。
Am J Physiol Renal Physiol. 2013 May 15;304(10):F1258-65. doi: 10.1152/ajprenal.00401.2012. Epub 2013 Mar 20.
5
Discovery and characterization of alamandine: a novel component of the renin-angiotensin system.发现并鉴定阿马林:肾素-血管紧张素系统的新组成部分。
Circ Res. 2013 Apr 12;112(8):1104-11. doi: 10.1161/CIRCRESAHA.113.301077. Epub 2013 Feb 27.
6
Proximal tubule-dominant transfer of AT(1a) receptors induces blood pressure responses to intracellular angiotensin II in AT(1a) receptor-deficient mice.近端小管优势转运 AT(1a) 受体导致血管紧张素 II 细胞内作用引起 AT(1a) 受体缺陷型小鼠血压反应。
Am J Physiol Regul Integr Comp Physiol. 2013 Apr 15;304(8):R588-98. doi: 10.1152/ajpregu.00338.2012. Epub 2013 Feb 20.
7
Cardiovascular effects of angiotensin A: a novel peptide of the renin-angiotensin system.血管紧张素A的心血管效应:肾素-血管紧张素系统的一种新型肽。
J Renin Angiotensin Aldosterone Syst. 2014 Dec;15(4):480-6. doi: 10.1177/1470320312474856. Epub 2013 Feb 5.
8
Opportunities for targeting the angiotensin-converting enzyme 2/angiotensin-(1-7)/mas receptor pathway in hypertension.靶向血管紧张素转换酶 2/血管紧张素-(1-7)/Mas 受体途径治疗高血压的机遇。
Curr Hypertens Rep. 2013 Feb;15(1):31-8. doi: 10.1007/s11906-012-0324-1.
9
Angiotensin II-independent upregulation of cyclooxygenase-2 by activation of the (Pro)renin receptor in rat renal inner medullary cells.血管紧张素 II 非依赖性通过激活大鼠肾髓质内细胞的(前)肾素受体上调环氧化酶-2。
Hypertension. 2013 Feb;61(2):443-9. doi: 10.1161/HYPERTENSIONAHA.112.196303. Epub 2012 Nov 26.
10
Mechanism of [Ca2+]i rise induced by angiotensin 1-7 in MDCK renal tubular cells.血管紧张素1-7诱导MDCK肾小管细胞内钙离子浓度升高的机制。
J Recept Signal Transduct Res. 2012 Dec;32(6):335-41. doi: 10.3109/10799893.2012.738690. Epub 2012 Nov 9.

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.

DOI:10.5527/wjn.v3.i3.64
PMID:25332897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4202493/
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。