The endocrine function of the heart

被引:207
作者
McGrath, MF [1 ]
de Bold, MLK [1 ]
de Bold, AJ [1 ]
机构
[1] Univ Ottawa, Inst Heart, Cardiovasc Endocrinol Lab, Ottawa, ON K1Y 4W7, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.tem.2005.10.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atrial cardiocytes in the heart of mammals produce in a regulated manner the polypeptide hormones atrial natriuretic factor (ANF, ANP) and brain natriuretic peptide (BNP). The biological actions of ANF and BNP are similar; they include the modulation of systems that tend to increase extracellular fluid volume and blood pressure, such as the renin-angiotensin system and the sympathetic nervous system. Additionally, both hormones have potent growth-regulating properties. ANF and BNP signal by activating membrane-bound guanylyl cyclase receptors, leading to an increase in intracellular cGMP and thus affecting the activity of cGMP-regulated enzymes and ion channels. Under chronic hemodynamic overload, cardiac ANF and BNP synthesis and secretion are increased. This increase is viewed as a cardioprotective mechanism, given the beneficial effects of ANF and BNP on cardiac preload, afterload and cardiovascular growth. As discussed in this review, some basic facts regarding the synthesis and secretion of ANF and BNP and their peripheral effects remain to be clarified. Nevertheless, at the clinical level, the elevation of circulating ANF and BNP in heart failure or following acute coronary syndromes has been shown to have diagnostic and prognostic implications. Moreover, these peptides themselves hold promise as therapeutic agents in the treatment of heart failure. Additional pharmaceutical applications might be gleaned from current preclinical and clinical studies showing beneficial effects of ANF or BNP in the treatment of hypertension, bronchospasm and in tissue remodeling following acute myocardial infarction.
引用
收藏
页码:469 / 477
页数:9
相关论文
共 116 条
[61]   CLONING AND SEQUENCE-ANALYSIS OF CDNA-ENCODING A PRECURSOR FOR PORCINE BRAIN NATRIURETIC PEPTIDE [J].
MAEKAWA, K ;
SUDOH, T ;
FURUSAWA, M ;
MINAMINO, N ;
KANGAWA, K ;
OHKUBO, H ;
NAKANISHI, S ;
MATSUO, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (01) :410-416
[62]   STRETCH-INDUCED ATRIAL-NATRIURETIC-FACTOR RELEASE UTILIZES A RAPIDLY DEPLETING POOL OF NEWLY SYNTHESIZED HORMONE [J].
MANGAT, H ;
DEBOLD, AJ .
ENDOCRINOLOGY, 1993, 133 (03) :1398-1403
[63]   Natriuretic and antialdosterone actions of chronic oral NEP inhibition during progressive congestive heart failure [J].
Martin, FL ;
Stevens, TL ;
Cataliotti, A ;
Schirger, JA ;
Borgeson, DD ;
Redfield, MM ;
Luchner, A ;
Burnett, JC .
KIDNEY INTERNATIONAL, 2005, 67 (05) :1723-1730
[64]   Discoordinate modulation of natriuretic peptides during acute cardiac allograft rejection in humans [J].
Masters, RG ;
Davies, RA ;
Veinot, JP ;
Hendry, PJ ;
Smith, SJ ;
de Bold, AJ .
CIRCULATION, 1999, 100 (03) :287-291
[65]   ANP in regulation of arterial pressure and fluid-electrolyte balance: lessons from genetic mouse models [J].
Melo, LG ;
Steinhelper, ME ;
Pang, SC ;
Tse, Y ;
Ackermann, U .
PHYSIOLOGICAL GENOMICS, 2000, 3 (01) :45-58
[66]   Effects of therapeutic doses of human atrial natriuretic peptide on load and myocardial performance in patients with congestive heart failure [J].
Mizuno, O ;
Onishi, K ;
Dohi, K ;
Motoyasu, M ;
Okinaka, T ;
Ito, M ;
Isaka, N ;
Nakano, T .
AMERICAN JOURNAL OF CARDIOLOGY, 2001, 88 (08) :863-866
[67]  
Murakami Y, 2002, CAN J CARDIOL, V18, P1294
[68]   Identification of the G protein-activating domain of the natriuretic peptide clearance receptor (NPR-C) [J].
Murthy, KS ;
Makhlouf, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (25) :17587-17592
[69]   Evidence for load-dependent and load-independent determinants of cardiac natriuretic peptide production [J].
Ogawa, T ;
Linz, W ;
Stevenson, M ;
Bruneau, BG ;
deBold, MLK ;
Chen, JH ;
Eid, H ;
Scholkens, BA ;
deBold, AJ .
CIRCULATION, 1996, 93 (11) :2059-2067
[70]  
OGAWA T, 1995, J MOL CELL CARDIOL, V27, pA219