Xu Jianchao, Desir Gary V
Department of Medicine, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Curr Opin Nephrol Hypertens. 2007 Jul;16(4):373-8. doi: 10.1097/MNH.0b013e3281bd8877.
Renalase is a secreted amine oxidase that metabolizes catecholamines. The approach used to identify this novel renal hormone will be discussed, as will the experimental data suggesting it regulates cardiovascular function, and its deficiency contributes to heightened cardiovascular risks in patients with chronic kidney disease.
The sympathetic nervous system is activated in chronic kidney disease and end-stage renal disease, and patients have a significant increase in cardiovascular disease. Parenteral administration of either native or recombinant renalase lowers blood pressure and heart rate by metabolizing circulating catecholamines. Plasma levels are markedly reduced in patients with chronic kidney disease and end-stage renal disease. Renalase deficiency occurs in salt-sensitive Dahl rats as they develop hypertension. Renalase inhibition by antisense RNA increases baseline blood pressure, and leads to an exaggerated blood pressure response to adrenergic stress. Most recently, two single nucleotide polymorphisms in the renalase gene were found to be associated with essential hypertension in humans.
The renalase pathway is a previously unrecognized mechanism for regulating circulating catecholamines, and, therefore, cardiac function, and blood pressure. Abnormalities in the renalase pathway are evident in animal models of chronic kidney disease and hypertension. Collectively, these data suggest that renalase replacement may be an important therapeutic modality.
肾酶是一种可代谢儿茶酚胺的分泌型胺氧化酶。本文将讨论鉴定这种新型肾激素所采用的方法,以及提示其调节心血管功能且其缺乏会导致慢性肾病患者心血管风险增加的实验数据。
慢性肾病和终末期肾病患者的交感神经系统被激活,心血管疾病显著增加。注射天然或重组肾酶可通过代谢循环中的儿茶酚胺来降低血压和心率。慢性肾病和终末期肾病患者的血浆水平明显降低。盐敏感型 Dahl 大鼠在发生高血压时会出现肾酶缺乏。反义 RNA 抑制肾酶会升高基础血压,并导致对肾上腺素能应激的血压反应过度。最近发现,肾酶基因中的两个单核苷酸多态性与人类原发性高血压有关。
肾酶途径是一种以前未被认识的调节循环儿茶酚胺、进而调节心脏功能和血压的机制。在慢性肾病和高血压动物模型中,肾酶途径存在异常。总体而言,这些数据表明肾酶替代可能是一种重要的治疗方式。