Chappell M C, Iyer S N, Diz D I, Ferrario C M
Hypertension and Vascular Disease Center, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1032, USA.
Braz J Med Biol Res. 1998 Sep;31(9):1205-12. doi: 10.1590/s0100-879x1998000900014.
Accumulating evidence suggests that angiotensin-(1-7)(Ang-(1-7)) is an important component of the renin-angiotensin system and that the actions of the peptide may either contribute to or oppose those of Ang II. Ang-(1-7) can be converted directly from Ang I bypassing prerequisite formation of Ang II. Formation of Ang-(1-7) is under the control of at least three endopeptidases depending on the tissue compartment and include neprilysin, thimet oligopeptidase and prolyl oligopeptidase. Both neprilysin and thimet oligopeptidase are also involved in the metabolism of bradykinin and the atrial natriuretic peptide. Moreover, recent studies suggest that in addition to Ang I and bradykinin, Ang-(1-7) is an endogenous substrate for angiotensin converting enzyme. These enzymatic pathways may contribute to a complex relationship between the hypertensive actions of Ang II and various vasodepressor peptides from either the renin-angiotensin system or other peptide systems. Ang-(1-7) is devoid of the vasoconstrictor, central pressor, or thirst-stimulating actions associated with Ang II. In fact, new findings reveal depressor, vasodilator, and antihypertensive actions that may be more apparent in hypertensive animals or humans. Thus, Ang-(1-7) may oppose the actions of Ang II directly or as a result of increasing prostaglandins or nitric oxide. In this review, we examine the mechanisms by which Ang-(1-7) may contribute to cardiovascular regulation.
越来越多的证据表明,血管紧张素-(1-7)(Ang-(1-7))是肾素-血管紧张素系统的重要组成部分,该肽的作用可能有助于或对抗Ang II的作用。Ang-(1-7)可以直接从Ang I转化而来,而无需先形成Ang II。Ang-(1-7)的形成受至少三种内肽酶的控制,这取决于组织部位,包括中性内肽酶、硫醚内肽酶和脯氨酰内肽酶。中性内肽酶和硫醚内肽酶也参与缓激肽和心房利钠肽的代谢。此外,最近的研究表明,除了Ang I和缓激肽外,Ang-(1-7)还是血管紧张素转换酶的内源性底物。这些酶促途径可能导致Ang II的高血压作用与肾素-血管紧张素系统或其他肽系统的各种血管舒张肽之间存在复杂的关系。Ang-(1-7)没有与Ang II相关的血管收缩、中枢升压或刺激口渴的作用。事实上,新的研究结果揭示了降压、血管舒张和抗高血压作用,这些作用在高血压动物或人类中可能更为明显。因此,Ang-(1-7)可能直接对抗Ang II的作用,或者通过增加前列腺素或一氧化氮来对抗其作用。在这篇综述中,我们研究了Ang-(1-7)可能参与心血管调节的机制。