期刊
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
卷 288, 期 4, 页码 H1674-H1682出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00945.2004
关键词
myocardial infarction; cardiac gene expression; renin-angiotensin system
This study was designed to test the hypothesis that blockade of the renin- angiotensin system improves cardiac function in congestive heart failure by preventing changes in gene expression of sarcoplasmic reticulum ( SR) proteins. We employed rats with myocardial infarction ( MI) to examine effects of an angiotensin- converting enzyme inhibitor, imidapril, on SR Ca2+ transport, protein content, and gene expression. Imidapril ( 1 mg (.) kg (-1) (.) day (-1)) was given for 4 wk starting 3 wk after coronary artery occlusion. Infarcted rats exhibited a fourfold increase in left ventricular end- diastolic pressure, whereas rates of pressure development and decay were decreased by 60 and 55%, respectively. SR Ca2+ uptake and Ca2+ pump ATPase, as well as Ca2+ release and ryanodine receptor binding activities, were depressed in the failing hearts; protein content and mRNA levels for Ca2+ pump ATPase, phospholamban, and ryanodine receptor were also decreased by similar to 55 -65%. Imidapril treatment of infarcted animals improved cardiac performance and attenuated alterations in SR Ca2+ pump and Ca2+ release activities. Changes in protein content and mRNA levels for SR Ca2+ pump ATPase, phospholamban, and ryanodine receptor were also prevented by imidapril treatment. Beneficial effects of imidapril on cardiac function and SR Ca2+ transport were not only seen at different intervals of MI but were also simulated by another angiotensinconverting enzyme inhibitor, enalapril, and an ANG II receptor antagonist, losartan. These results suggest that blockade of the reninangiotensin system may increase the abundance of mRNA for SR proteins and, thus, may prevent the depression in SR Ca2+ transport and improve cardiac function in congestive heart failure due to MI.
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