Central mineralocorticoid receptor blockade improves volume regulation and reduces sympathetic drive in heart failure

被引:128
作者
Francis, J
Weiss, RM
Wei, SG
Johnson, AK
Beltz, TG
Zimmerman, K
Felder, RB
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Psychol, Iowa City, IA 52242 USA
[3] Univ Iowa, Coll Med, Dept Vet Affairs Med Ctr, Res Serv, Iowa City, IA 52242 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2001年 / 281卷 / 05期
关键词
myocardial infarction; renin-angiotensin system; aldosterone; spironolactone; rat;
D O I
10.1152/ajpheart.2001.281.5.H2241
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mineralocorticoid (MC) receptor antagonist spironolactone (SL) improves morbidity and mortality in patients with congestive heart failure (CHF). We tested the hypothesis that the central nervous system actions of SL contribute to its beneficial effects. SL (100 ng/h for 28 days) or ethanol vehicle (VEH) was administered intracerebroventricularly or intraperitoneally to rats with CHF induced by coronary artery ligation (CL) and to SHAM-operated controls. The intracerebroventricular SL treatment prevented the increase in sodium appetite and the decreases in sodium and water excretion observed within a week of CL in VEH-treated CHF rats. Intraperitoneal SL also improved volume regulation in the CHF rats, but only after 3 wk of treatment. Four weeks of SL treatment, either intracerebroventricularly or intraperitoneally, ameliorated both the increase in sympathetic drive and the impaired baroreflex function observed in VEH-treated CHF rats. These findings suggest that activation of MC receptors in the central nervous system plays a critical role in the altered volume regulation and augmented sympathetic drive that characterize clinical heart failure.
引用
收藏
页码:H2241 / H2251
页数:11
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