Cardiovascular Effects of Insulin-Like Growth Factor-1 and Growth Hormone in Chronic Left Ventricular Failure in the Rat

医学 内科学 心脏病学 心肌梗塞 心室重构 心力衰竭 射血分数 血管阻力 内分泌学 心输出量 安慰剂 舒张末期容积 舒张期 冲程容积 血流动力学 血压 替代医学 病理
作者
Robert Duerr,M. Dan McKirnan,Ronald Gim,Ross Clark,Kenneth R. Chien,John Ross
出处
期刊:Circulation [Lippincott Williams & Wilkins]
卷期号:93 (12): 2188-2196 被引量:152
标识
DOI:10.1161/01.cir.93.12.2188
摘要

Background Insulin-like growth factor-1 (IGF-1) appears to have favorable cardiac effects associated with left ventricular remodeling early after myocardial infarction in the rat. The present study was designed to determine whether IGF-1 combined with growth hormone would be beneficial later as well, when infarct healing and cardiac remodeling have occurred. Methods and Results Four weeks after coronary occlusion, 36 rats were randomized to IGF-1 (3 mg·kg −1 ·d −1 ) plus growth hormone (0.1 mg BID) or to placebo for 4 weeks. Treated rats had significant increases in body weight (22%), while the ratio of heart weight to body weight was unchanged. Under anesthesia, cardiac output (fluorescent microspheres) increased 46%, and systemic vascular resistance decreased by 21% ( P <.001) in the treated group; a significant (22%) increase of the cardiac index was limited to treated rats with large myocardial infarctions. Small increases in the reduced left ventricular ejection fractions and left ventricular dP/dt max values with treatment were not significant. Treated rats showed a borderline (16%) increase in left ventricular end-diastolic volume (angiography), whereas the ratio of left ventricular end-diastolic volume to body weight was reduced in the treated group. Conclusions IGF-1 plus growth hormone administered to rats with left ventricular failure starting 1 month after MI was associated with substantial body growth, decreased systemic vascular resistance, and increased cardiac output. The failing heart also underwent treatment-induced increases in left and right ventricular weights in proportion to body growth, but left ventricular remodeling was minor, and a decrease in the ratio of left ventricular end-diastolic volume to body weight reflected relatively less chamber dilation compared with controls. A significant interaction between size of the myocardial infarction and treatment was observed for several variables, and IGF-1 and growth hormone increased the cardiac index ( P <.035) in rats with a large myocardial infarction.

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