Ramírez-Expósito María Jesús, Martínez-Martos José Manuel
Department of Health Sciences/Physiology, Faculty of Experimental and Health Sciences, University of Jaén, Jaen, Spain.
Heart Fail Rev. 2008 Sep;13(3):355-65. doi: 10.1007/s10741-008-9082-1. Epub 2008 Jan 24.
Hypertension is the major risk factor for coronary heart disease, stroke, and renal disease. Also, it is probably the most important risk factor for peripheral vascular disease and vascular dementia. Although hypertension occurs in both men and women, gender differences have been observed. However, whether sex hormones are responsible for the observed gender-associated differences in arterial blood pressure, and which is their mechanism of action, remains unclear. Local and circulating renin-angiotensin systems (RAS) are examples of systems that may be involved in the pathogenesis of hypertension. Classically, angiotensin II (Ang II) has been considered as the effector peptide of the RAS, but Ang II is not the only active peptide. Several of its degradation products, including angiotensin III (Ang III) and angiotensin IV (Ang IV) also possess biological functions. These peptides are formed via the activity of several aminopeptidases. This review will briefly summarize what is known about gender differences in RAS-regulating aminopeptidase activities, their relationship with sex hormones, and their potential role in controlling blood pressure acting through local and circulating RAS.
高血压是冠心病、中风和肾病的主要危险因素。此外,它可能是外周血管疾病和血管性痴呆最重要的危险因素。虽然高血压在男性和女性中都有发生,但已观察到性别差异。然而,性激素是否导致了所观察到的动脉血压的性别相关差异,以及它们的作用机制是什么,仍不清楚。局部和循环肾素-血管紧张素系统(RAS)是可能参与高血压发病机制的系统实例。传统上,血管紧张素II(Ang II)被认为是RAS的效应肽,但Ang II不是唯一的活性肽。它的几种降解产物,包括血管紧张素III(Ang III)和血管紧张素IV(Ang IV)也具有生物学功能。这些肽是通过几种氨肽酶的活性形成的。本综述将简要总结关于RAS调节氨肽酶活性的性别差异、它们与性激素的关系以及它们通过局部和循环RAS控制血压的潜在作用的已知信息。