Relaxin and Nitric Oxide Signalling

被引:36
作者
Baccari, M. C. [1 ]
Bani, D. [2 ]
机构
[1] Univ Florence, Dept Physiol Sci, I-50134 Florence, Italy
[2] Univ Florence, Dept Anat Histol & Forens Med, I-50134 Florence, Italy
关键词
Relaxin; nitric oxide;
D O I
10.2174/138920308786733921
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peptide hormone relaxin (RLX) has been shown to exert a variety of functions in both reproductive and non-reproductive tissues. The molecular mechanism of RLX on its target cells appears to involve multiple intracellular signalling systems, including the nitric oxide ( NO) pathway. NO is an ubiquitous molecule synthesised from L-arginine under the catalytic action of different nitric oxide synthase ( NOS) isoforms and its altered production has been reported to be involved in several diseases. RLX has been demonstrated to promote NO biosynthesis by up-regulating NOS expression; its influence on the different NOS appears to depend on the cell type studied. In addition to its physiological roles, RLX has been postulated as a potential therapeutic agent in several diseases. In particular, based on its property to promote NO biosynthesis, RLX may be regarded as a therapeutic tool in diseases characterized pathogenically by an impaired NO production. The aim of the present mini-review is to summarize and discuss the pathophysiological actions of RLX, strictly related to its ability to activate the endogenous NO pathway in reproductive and non-reproductive target organs.
引用
收藏
页码:638 / 645
页数:8
相关论文
共 125 条
  • [91] Nistri Silvia, 2007, Cardiovascular & Hematological Agents in Medicinal Chemistry, V5, P101, DOI 10.2174/187152507780363179
  • [92] Relaxin receptors and nitric oxide synthases: Search for the missing link
    Silvia Nistri
    Daniele Bani
    [J]. Reproductive Biology and Endocrinology, 1 (1)
  • [93] Relaxin is essential for renal vasodilation during pregnancy in conscious rats
    Novak, J
    Danielson, LA
    Kerchner, LJ
    Sherwood, OD
    Ramirez, RJ
    Moalli, PA
    Conrad, KP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (11) : 1469 - 1475
  • [94] Myogenic reactivity is reduced in small renal arteries isolated from relaxin-treated rats
    Novak, J
    Ramirez, RJJ
    Gandley, RE
    Sherwood, OD
    Conrad, KP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (02) : R349 - R355
  • [95] OSHEROFF PL, 1993, J BIOL CHEM, V268, P15193
  • [96] Effects of relaxin on rat atrial myocytes .1. Inhibition of I-to via PKA-dependent phosphorylation
    PiedrasRenteria, ES
    Sherwood, OD
    Best, PM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (04): : H1791 - H1797
  • [97] Relaxin potentiates the expression of inducible nitric oxide synthase by endothelial cells from human umbilical vein in in vitro culture
    Quattrone, S
    Chiappini, L
    Scapagnini, G
    Bigazzi, B
    Bani, D
    [J]. MOLECULAR HUMAN REPRODUCTION, 2004, 10 (05) : 325 - 330
  • [98] NITRERGIC TRANSMISSION - NITRIC-OXIDE AS A MEDIATOR OF NONADRENERGIC, NONCHOLINERGIC NEUROEFFECTOR TRANSMISSION
    RAND, MJ
    [J]. CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1992, 19 (03): : 147 - 169
  • [99] Endothelial function, vascular reactivity and gender differences in the cardiovascular system
    Sader, MA
    Celermajer, DS
    [J]. CARDIOVASCULAR RESEARCH, 2002, 53 (03) : 597 - 604
  • [100] Drugs of the future: the hormone relaxin
    Samuel, C. S.
    Hewitson, T. D.
    Unemori, E. N.
    Tang, M. L. -K.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (12) : 1539 - 1557