Defence Institute of Physiology and Allied Sciences, Defence Research and Development Organization, Lucknow Road, Timarpur, Delhi, India.
J Pharm Pharmacol. 2010 Dec;62(12):1729-39. doi: 10.1111/j.2042-7158.2010.01163.x. Epub 2010 Oct 4.
Acute systemic hypoxia induces delayed cardioprotection against ischaemia-reperfusion injury in the heart. As cobalt chloride (CoCl₂) 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.
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).
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 1α (HIF-1α) 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.
The results showed that hypoxic preconditioning with cobalt induces acclimatization by up-regulation of hemeoxygenase 1 and metallothionein 1 via HIF-1 stabilization.
急性全身缺氧可诱导心脏对缺血再灌注损伤产生延迟性保护作用。已知氯化钴(CoCl₂)可引起类似缺氧的反应,因此假设这种化学物质可以模拟预处理效应,并促进大鼠心脏对低氧环境的适应。
用蒸馏水或氯化钴(12.5mg Co/kg,连续 7 天)处理雄性 Sprague-Dawley 大鼠,然后将其暴露于模拟海拔 7622 米的环境中不同时间(1、2、3 和 5 天)。
钴的低氧预处理显著减轻了低氧诱导的氧化损伤,表现为自由基(活性氧)生成、脂质和蛋白质氧化减少。有趣的是,观察到的效果是由于抗氧化蛋白血红素加氧酶和金属硫蛋白表达增加所致,因为抗氧化酶活性没有明显变化。钴的低氧预处理增加了缺氧诱导因子 1α(HIF-1α)的表达以及 HIF-1 DNA 结合活性,这进一步导致 HIF-1 调节的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。与未进行预处理的缺氧动物相比,预处理动物的心脏中乳酸脱氢酶活性和乳酸水平显著降低。
结果表明,钴的低氧预处理通过 HIF-1 稳定诱导血红素加氧酶 1 和金属硫蛋白 1 的上调来诱导适应。