Samuel Chrishan S, Du Xiao-Jun, Bathgate Ross A D, Summers Roger J
Howard Florey Institute, University of Melbourne, Victoria 3010, Australia; Department of Biochemistry and Molecular Biology, University of Melbourne, Victoria 3010, Australia.
Pharmacol Ther. 2006 Nov;112(2):529-52. doi: 10.1016/j.pharmthera.2005.05.012. Epub 2006 Jul 11.
Although originally characterised as a reproductive hormone, relaxin has emerged as a multi-functional endocrine and paracrine factor that plays a number of important roles in several organs, including the normal and diseased cardiovascular system. The recent discovery of the H3/relaxin-3 gene, and the elusive receptors for relaxin (Relaxin family peptide receptor; RXFP1) and relaxin-3 (RXFP3/RXFP4) have led to the re-classification of a distinct relaxin peptide/receptor family. Additionally, the identification of relaxin and RXFP1 mRNA and/or relaxin binding sites in the heart and blood vessels has confirmed that the cardiovascular system is a target for relaxin peptides. While evidence for the production of relaxins within the cardiovascular system is limited, several studies have established that the relaxin genes are upregulated in the diseased human and rodent heart where they likely act as cardioprotective agents. The ability of relaxin to protect the heart is most likely mediated via its antifibrotic, anti-hypertrophic, anti-inflammatory and vasodilatory actions, but it may also directly stimulate myocardial regeneration and repair. This review describes relaxin and its primary receptor (RXFP1) in relation to the roles and effects of relaxin in the normal and pathological cardiovascular system. It is becoming increasingly clear that relaxin has a number of diverse physiological and pathological roles in the cardiovascular system that may have important therapeutic and clinical implications.
尽管松弛素最初被表征为一种生殖激素,但它已成为一种多功能的内分泌和旁分泌因子,在包括正常和患病心血管系统在内的多个器官中发挥着许多重要作用。最近发现的H3/松弛素-3基因,以及难以捉摸的松弛素受体(松弛素家族肽受体;RXFP1)和松弛素-3受体(RXFP3/RXFP4),导致了一个独特的松弛素肽/受体家族的重新分类。此外,在心脏和血管中鉴定出松弛素和RXFP1 mRNA和/或松弛素结合位点,证实了心血管系统是松弛素肽的作用靶点。虽然心血管系统内产生松弛素的证据有限,但多项研究已证实,在患病的人类和啮齿动物心脏中,松弛素基因上调,它们可能起到心脏保护剂的作用。松弛素保护心脏的能力很可能是通过其抗纤维化、抗肥大、抗炎和血管舒张作用介导的,但它也可能直接刺激心肌再生和修复。本综述描述了松弛素及其主要受体(RXFP1)与松弛素在正常和病理心血管系统中的作用及影响的关系。越来越清楚的是,松弛素在心血管系统中具有多种不同的生理和病理作用,这可能具有重要的治疗和临床意义。