Xia Huijing, Lazartigues Eric
Department of Pharmacology and Experimental Therapeutics and Cardiovascular Center of Excellence, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
J Neurochem. 2008 Dec;107(6):1482-94. doi: 10.1111/j.1471-4159.2008.05723.x. Epub 2008 Nov 5.
Angiotensin (Ang)-converting enzyme (ACE) 2 cleaves Ang-II into the vasodilator peptide Ang-(1-7), thus acting as a pivotal element in balancing the local effects of these peptides. ACE2 has been identified in various tissues and is supposed to be a modulator of cardiovascular function. Decreases in ACE2 expression and activity have been reported in models of hypertension, heart failure, atherosclerosis, diabetic nephropathy and others. In addition, the expression level and/or activity are affected by other renin-angiotensin system components (e.g., ACE and AT1 receptors). Local inhibition or global deletion of brain ACE2 induces a reduction in baroreflex sensitivity. Moreover, ACE2-null mice have been shown to exhibit either blood pressure or cardiac dysfunction phenotypes. On the other hand, over-expression of ACE2 exerts protective effects in local tissues, including the brain. In this review, we will first summarize the major findings linking ACE2 to cardiovascular function in the periphery then focus on recent discoveries related to ACE2 in the CNS. Finally, we will unveil new tools designed to address the importance of central ACE2 in various diseases, and discuss the potential for this carboxypeptidase as a new target in the treatment of hypertension and other cardiovascular diseases.
血管紧张素(Ang)转换酶(ACE)2可将Ang-II裂解为血管舒张肽Ang-(1-7),因此在平衡这些肽的局部作用中起着关键作用。ACE2已在多种组织中被鉴定出来,被认为是心血管功能的调节因子。在高血压、心力衰竭、动脉粥样硬化、糖尿病肾病等模型中,已报道ACE2的表达和活性降低。此外,其表达水平和/或活性还受其他肾素-血管紧张素系统成分(如ACE和AT1受体)的影响。局部抑制或整体敲除脑内ACE2会导致压力反射敏感性降低。此外,已证明ACE2基因敲除小鼠表现出血压或心脏功能障碍的表型。另一方面,ACE2的过表达在包括脑在内的局部组织中发挥保护作用。在本综述中,我们将首先总结将ACE2与外周心血管功能联系起来的主要发现,然后重点关注中枢神经系统中与ACE2相关的最新发现。最后,我们将介绍旨在阐明中枢ACE2在各种疾病中的重要性的新工具,并讨论这种羧肽酶作为高血压和其他心血管疾病治疗新靶点的潜力。