Molecular mechanisms of myocardial remodeling. The role of aldosterone

被引:172
作者
Delcayre, C [1 ]
Swynghedauw, B [1 ]
机构
[1] Hop Lariboisiere, CNRS, INSERM U217, F-75475 Paris, France
关键词
aldosterone; cardiac remodeling; evolutionary medicine; fibrosis; renin-angiotensin system; myocardial infarction; heart failure;
D O I
10.1006/jmcc.2002.2088
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Cardiac remodeling, CR, is a complex and rather controversial issue and results from the, sometimes opposite, trophic effects of pure mechanical overload, and susceptibility factors, as senescence, aetiologies, as ischemia, and the neurohormonal reaction. The molecular mechanisms of CR are heritable and had, in the past, increased fitness, as such CR belongs to evolutionary medicine. Aldosterone production plays an important role in the remodeling of the heart. (i) There are numerous evidences that aldosterone induces fibrosis in all the cardiovascular system in the presence of high sodium diet. The aldosterone receptor is a transcriptional factor and the pathways that lead to aldosterone-induced fibrosis are multiple. Aldosterone induces the expression of the angiotensin II receptors subtype I and that of the glucocorticoid receptors. The RALES trial have recently evidenced a significant beneficial effect of spironolactone on both mortality and morbidity in heart failure, and a substudy has shown that these effects are linked to a reduction is fibrosis. (ii) An intracardiac production of aldosterone and corticosterone have been evidenced in the rat. Aldosterone production is regulated by low sodium/high potassium diets and by angiotensin II and is predominant in atria, cardiac production is low as compared to the adrenal production, nevertheless it results in high local concentrations, just like angiotensin II. In rats, myocardial infarction activates aldosterone production and this activation is prevented by losartan. Heart failure, in human, activates aldosterone production and is accompanied by a significant increase of the arteriovenous difference in aldosterone by the myocardium. To conclude (i) after a myocardial infarction local production of aldosterone and angiotensin II are likely to play a major role in regulating collagen turnover and fibrous tissue formation; (ii) during heart failure, the activation of adrenal and cardiovascular production of aldosterone belongs to the neurohormonal reaction and would play a detrimental role in producing reactive fibrosis. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1577 / 1584
页数:8
相关论文
共 51 条
[1]
Alpert N.R., 1992, HEART CARDIOVASCULAR, P111
[2]
[Anonymous], 1999, EVOLUTIONARY MED
[3]
Effects of sustained low-flow ischemia on myocardial function and calcium-regulating proteins in adult and senescent rat hearts [J].
Assayag, P ;
Charlemagne, D ;
Marty, I ;
de Leiris, J ;
Lompré, AM ;
Boucher, F ;
Valère, PE ;
Lortet, S ;
Swynghedauw, B ;
Besse, S .
CARDIOVASCULAR RESEARCH, 1998, 38 (01) :169-180
[4]
Bénitah JP, 1999, CIRC RES, V85, P1139
[5]
IS THE SENESCENT HEART OVERLOADED AND ALREADY FAILING [J].
BESSE, S ;
DELCAYRE, C ;
CHEVALIER, B ;
HARDOUIN, S ;
HEYMES, C ;
BOURGEOIS, F ;
MOALIC, JM ;
SWYNGHEDAUW, B .
CARDIOVASCULAR DRUGS AND THERAPY, 1994, 8 (04) :581-587
[6]
COLLAGEN-METABOLISM IN CULTURED ADULT-RAT CARDIAC FIBROBLASTS - RESPONSE TO ANGIOTENSIN-II AND ALDOSTERONE [J].
BRILLA, CG ;
ZHOU, GP ;
MATSUBARA, L ;
WEBER, KT .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1994, 26 (07) :809-820
[7]
REMODELING OF THE RAT RIGHT-AND-LEFT-VENTRICLES IN EXPERIMENTAL-HYPERTENSION [J].
BRILLA, CG ;
PICK, R ;
TAN, LB ;
JANICKI, JS ;
WEBER, KT .
CIRCULATION RESEARCH, 1990, 67 (06) :1355-1364
[8]
MYOCARDIAL FIBROSIS IN THE RAT WITH MINERALOCORTICOID EXCESS - PREVENTION OF SCARRING BY AMILORIDE [J].
CAMPBELL, SE ;
JANICKI, JS ;
MATSUBARA, BB ;
WEBER, KT .
AMERICAN JOURNAL OF HYPERTENSION, 1993, 6 (06) :487-495
[9]
CHARLEMAGNE D, 1994, J BIOL CHEM, V269, P1541
[10]
PERINATAL CHANGES IN PLASMA AND ADRENAL CORTICOSTERONE AND ALDOSTERONE CONCENTRATIONS IN MOUSE [J].
DALLE, M ;
GIRY, J ;
GAY, M ;
DELOST, P .
JOURNAL OF ENDOCRINOLOGY, 1978, 76 (02) :303-309