...
首页> 外文期刊>Journal of Pharmacy and Pharmacology >Hypoxic preconditioning facilitates acclimatization to hypobaric hypoxia in rat heart.
【24h】

Hypoxic preconditioning facilitates acclimatization to hypobaric hypoxia in rat heart.

机译:缺氧预处理可促进大鼠心脏的低压缺氧适应。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVES: Acute systemic hypoxia induces delayed cardioprotection against ischaemia-reperfusion injury in the heart. As cobalt chloride (CoCl) is known to elicit hypoxia-like responses, it was hypothesized that this chemical would mimic the preconditioning effect and facilitate acclimatization to hypobaric hypoxia in rat heart. METHODS: Male Sprague-Dawley rats treated with distilled water or cobalt chloride (12.5 mg Co/kg for 7 days) were exposed to simulated altitude at 7622 m for different time periods (1, 2, 3 and 5 days). KEY FINDINGS: Hypoxic preconditioning with cobalt appreciably attenuated hypobaric hypoxia-induced oxidative damage as observed by a decrease in free radical (reactive oxygen species) generation, oxidation of lipids and proteins. Interestingly, the observed effect was due to increased expression of the antioxidant proteins hemeoxygenase and metallothionein, as no significant change was observed in antioxidant enzyme activity. Hypoxic preconditioning with cobalt increased hypoxia-inducible factor 1alpha (HIF-1alpha) expression as well as HIF-1 DNA binding activity, which further resulted in increased expression of HIF-1 regulated genes such as erythropoietin, vascular endothelial growth factor and glucose transporter. A significant decrease was observed in lactate dehydrogenase activity and lactate levels in the heart of preconditioned animals compared with non-preconditioned animals exposed to hypoxia. CONCLUSIONS: The results showed that hypoxic preconditioning with cobalt induces acclimatization by up-regulation of hemeoxygenase 1 and metallothionein 1 via HIF-1 stabilization.
机译:目的:急性全身性缺氧诱导心脏保护作用,以防止心脏缺血再灌注损伤。由于已知氯化钴(CoCl)会引起类似缺氧的反应,因此推测该化学物质会模仿预处理效应,并有助于适应大鼠心脏的低压缺氧。方法:用蒸馏水或氯化钴(12.5 mg Co / kg进行7天)处理的雄性Sprague-Dawley大鼠在不同时间段(1、2、3和5天)暴露于7622 m的模拟高度。主要发现:通过自由基(活性氧)生成的减少,脂质和蛋白质的氧化所观察到的,用钴进行的缺氧预处理可明显减轻低压缺氧引起的氧化损伤。有趣的是,观察到的效果是由于抗氧化剂蛋白血氧合酶和金属硫蛋白的表达增加,因为未观察到抗氧化剂酶活性的显着变化。钴的缺氧预处理增加了缺氧诱导因子1α(HIF-1alpha)的表达以及HIF-1 DNA的结合活性,这进一步导致了HIF-1调控基因(如促红细胞生成素,血管内皮生长因子和葡萄糖转运蛋白)的表达增加。与暴露于低氧的非预处理动物相比,在预处理动物的心脏中观察到乳酸脱氢酶活性和乳酸水平的显着降低。结论:结果表明,通过HIF-1稳定作用,钴的低氧预处理可通过上调血氧合酶1和金属硫蛋白1来诱导适应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号