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缺氧和葡萄糖剥夺对大鼠心脏内皮细胞原代培养物的损伤。

Injury to primary cultures of rat heart endothelial cells by hypoxia and glucose deprivation.

作者信息

Acosta D, Li C P

出版信息

In Vitro. 1979 Nov;15(11):929-34. doi: 10.1007/BF02618051.

Abstract

Primary cultures of rat heart endothelial cells were subjected to simulated conditions of ischemia: hyposia and glucose deprivation for 4 and 24 hr. Cellular injury was evaluated by measuring changes in viability, total protein, cellular morphology, and leakage of cytoplasmic enzymes from the cells into the culture medium. Deprivation of oxygen and glucose for 4 or 24 hr did not lethally injure the cells as noted by no change in cell viability, morphology, and total protein when compared to controls. However, reversible or non-lethal cellular injury was produced as reflected by a significant release of lactate dehydrogenase (LDH) from the cells into the medium after treatment with hypoxia and glucose deprivation for 4 or 24 hr. When the cultures were deprived of glucose, but were oxygenated, cellular injury was not evident after 24 hr. Deprivation of oxygen but not glucose resulted in significant loss of LDH after 4 or 24 hr. When the cultures were allowed to recover after oxygen and glucose deprivation in complete medium containing 1000 mg glucose per 1 and a normal atmosphere of 20% O2, they had levels of LDH leakage comparable to those of control cultures.

摘要

大鼠心脏内皮细胞的原代培养物被置于模拟缺血条件下

低氧和葡萄糖剥夺4小时和24小时。通过测量细胞活力、总蛋白、细胞形态的变化以及细胞质酶从细胞渗漏到培养基中的情况来评估细胞损伤。与对照组相比,4小时或24小时的缺氧和葡萄糖剥夺并未导致细胞发生致命损伤,这表现为细胞活力、形态和总蛋白没有变化。然而,在用缺氧和葡萄糖剥夺处理4小时或24小时后,细胞内乳酸脱氢酶(LDH)大量释放到培养基中,这反映出细胞发生了可逆性或非致命性损伤。当培养物被剥夺葡萄糖但进行了充氧处理时,24小时后细胞损伤并不明显。仅缺氧而不剥夺葡萄糖在4小时或24小时后会导致LDH显著损失。当培养物在含有每升1000毫克葡萄糖且氧气含量为20%的正常大气环境的完全培养基中经历缺氧和葡萄糖剥夺后恢复时,它们的LDH渗漏水平与对照培养物相当。

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