3.8 Article

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

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/S1071-5576(03)00074-1

关键词

fetus; chronic hypoxia; heart; ischemia-reperfusion injury; apoptosis

资金

  1. NHLBI NIH HHS [HL-67745, HL-57787] Funding Source: Medline
  2. NICHD NIH HHS [HD-31226] Funding Source: Medline

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据