'Relaxin' the stiffened heart and arteries: The therapeutic potential for relaxin in the treatment of cardiovascular disease

被引:75
作者
Samuel, Chrishan S.
Du, Xiao-Jun
Bathgate, Ross A. D.
Summers, Roger J.
机构
[1] Monash Univ, Dept Pharmacol, Clayton, Vic 3800, Australia
[2] Univ Melbourne, Howard Florey Inst Expt Physiol & Med, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Dept Biochem & Mol Biol, Melbourne, Vic 3010, Australia
[4] Baker Heart Res Inst, Melbourne, Vic 3004, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
H1; relaxin; H2; H3; LGR7; RXFP1;
D O I
10.1016/j.pharmthera.2005.05.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 reclassification of a distinct relaxin peptide/receptor family. Additionally, the identification of relaxin and RXFPI 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. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:529 / 552
页数:24
相关论文
共 195 条
[21]   RELAXIN-DEPENDENT ADENOSINE-3',5'-MONOPHOSPHATE CONCENTRATION CHANGES IN MOUSE PUBIC SYMPHYSIS [J].
BRADDON, SA .
ENDOCRINOLOGY, 1978, 102 (04) :1292-1299
[22]   The trap-like relaxin-binding site of the leucine-rich G-protein-coupled receptor 7 [J].
Büllesbach, EE ;
Schwabe, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (14) :14051-14056
[23]   Restricted, but abundant, expression of the novel rat gene-3 (R3) relaxin in the dorsal tegmental region of brain [J].
Burazin, TCD ;
Bathgate, RAD ;
Macris, M ;
Layfield, S ;
Gundlach, AL ;
Tregear, GW .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (06) :1553-1557
[24]   Hypertension in mice lacking the proatrial natriuretic peptide convertase corin [J].
Chan, JCY ;
Knudson, O ;
Wu, FY ;
Morser, J ;
Dole, WP ;
Wu, QY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) :785-790
[25]   TARGET TISSUES FOR RELAXIN IN THE RAT - TISSUE DISTRIBUTION OF INJECTED I-125-LABELED RELAXIN AND TISSUE CHANGES IN ADENOSINE-3',5'-MONOPHOSPHATE LEVELS AFTER INVITRO RELAXIN INCUBATION [J].
CHEAH, SH ;
SHERWOOD, OD .
ENDOCRINOLOGY, 1980, 106 (04) :1203-1209
[26]   THE EFFECT OF RELAXIN ON CYCLIC ADENOSINE 3', 5'-MONOPHOSPHATE CONCENTRATIONS IN HUMAN ENDOMETRIAL GLANDULAR EPITHELIAL-CELLS [J].
CHEN, G ;
HUANG, JR ;
TSENG, L .
BIOLOGY OF REPRODUCTION, 1988, 39 (03) :519-525
[27]   Emerging role of relaxin in renal and cardiovascular function [J].
Conrad, KP ;
Novak, J .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2004, 287 (02) :R250-R261
[28]   Endothelin mediates renal vasodilation and hyperfiltration during pregnancy in chronically instrumented conscious rats [J].
Conrad, KP ;
Gandley, RE ;
Ogawa, T ;
Nakanishi, S ;
Danielson, LA .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 276 (05) :F767-F776
[29]   Relaxin modifies systemic arterial resistance and compliance in conscious, nonpregnant rats [J].
Conrad, KP ;
Debrah, DO ;
Novak, J ;
Danielson, LA ;
Shroff, SG .
ENDOCRINOLOGY, 2004, 145 (07) :3289-3296
[30]   Mechanisms of renal vasodilation and hyperfiltration during pregnancy [J].
Conrad, KP .
JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION, 2004, 11 (07) :438-448