Effect of fetal hypoxia on heart susceptibility to ischemia and reperfusion injury in the adult rat

被引:158
作者
Li, GH [1 ]
Xiao, YH [1 ]
Estrella, JL [1 ]
Ducsay, CA [1 ]
Gilbert, RD [1 ]
Zhang, LB [1 ]
机构
[1] Loma Linda Univ, Sch Med, Ctr Perinatal Biol, Dept Pharmacol & Physiol, Loma Linda, CA 92350 USA
关键词
fetus; chronic hypoxia; heart; ischemia-reperfusion injury; apoptosis; NITRIC-OXIDE SYNTHASE; CARDIAC MYOCYTES; PRECONDITIONING DECREASES; INFARCT SIZE; ISCHEMIA/REPERFUSION INJURY; MYOCARDIAL-ISCHEMIA; SHOCK PROTEINS; APOPTOSIS; EXPRESSION; INCREASES;
D O I
10.1016/S1071-5576(03)00074-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Epidemiologic studies showed an association between adverse intrauterine environment and ischemic heart disease in the adult. We tested the hypothesis that prenatal hypoxia increased the susceptibility of adult heart to ischemia-reperfusion (I-R) injury. METHODS: Time-dated pregnant rats were divided between normoxic and hypoxic (10.5% oxygen from day 15 to 21) groups. Hearts of 6-month-old male progeny were studied using Langendorff preparation and were subjected to two protocols of I-R: 10 minutes of ischemia and 3 hours of reperfusion (I-R-10) or 25 minutes of ischemia and 3 hours of reperfusion (I-R-25). RESULTS: Prenatal hypoxia did not change basal left ventricular (LV) function. I-R-10 produced myocardial stunning and a transient decrease in LV function in control hearts but caused myocardial infarction and a persistent decrease in postischemic recovery of LV function in hypoxic hearts. I-R-25 caused myocardial infarction in both control and hypoxic hearts, which was significantly higher in hypoxic hearts. The postischemic recovery of LV function was significantly reduced in hypoxic hearts. I-R-25-induced activation of caspase-3 and apoptosis in the left ventricle were significantly higher in hypoxic than control hearts. There was a significant decrease in LV heat shock protein 70 and endothelial nitric oxide synthase levels in hypoxic hearts. Prenatal hypoxia did not change beta(1)-adrenoreceptor levels but significantly increased beta(2)-adrenoreceptor in the left ventricle. In addition, it increased G(s)alpha but decreased G(i)alpha. CONCLUSION: Prenatal chronic hypoxia increases the susceptibility of adult heart to I-R injury. Several possible mechanisms may be involved, including an increase in beta(2)-adrenoreceptor and the G(s)alpha/G(i)alpha. ratio, and a decrease in heat shock protein 70 and endothelial nitric oxide synthase in the left ventricle. (J Soc Gynecol Invesug 2003;10:265-74) Copyright (C) 2003 by the Societyfor Gynecologic Investigation.
引用
收藏
页码:265 / 274
页数:10
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