Acosta D, Puckett M, Li C P
In Vitro. 1980 Feb;16(2):93-6. doi: 10.1007/BF02831498.
An in vitro model to study myocardial cell injury was developed with primary monolayer cultures of rat myocardial cells. Two important conditions associated with myocardial ischemia were simulated by depriving the cultures of oxygen and glucose for a specified period of time. Cellular injury caused by hypoxia and glucose deprivation resulted in significant leakage of lactate dehydrogenase (LDH) from the cells into the culture medium. The cells were not lethally injured by treatments as reflected by a lack of change in cell viability and protein content when compared to controls. Pretreatment of cultures with methylprednisolone for 24 hr provided protection to the cells when challenged by hypoxia and glucose deprivation. Methylprednisolone exhibited a dose-response effect in reducing LDH leakage in cultures, which were subsequently deprived of oxygen and glucose for 4 hr. Similar pretreatment with hydrocortisone had no effect in limiting cellular injury in hypoxic and glucose-deprived cultures.
利用大鼠心肌细胞的原代单层培养建立了一种用于研究心肌细胞损伤的体外模型。通过在特定时间段内剥夺培养物中的氧气和葡萄糖来模拟与心肌缺血相关的两个重要条件。缺氧和葡萄糖剥夺导致的细胞损伤致使乳酸脱氢酶(LDH)从细胞大量泄漏到培养基中。与对照组相比,细胞活力和蛋白质含量没有变化,这表明这些处理并未对细胞造成致命损伤。用甲基泼尼松龙对培养物进行24小时预处理,在受到缺氧和葡萄糖剥夺挑战时可为细胞提供保护。甲基泼尼松龙在减少随后被剥夺氧气和葡萄糖4小时的培养物中LDH泄漏方面表现出剂量反应效应。用氢化可的松进行类似的预处理对限制缺氧和葡萄糖剥夺培养物中的细胞损伤没有效果。