Rosenberger L B, Jacobs L W, Stanton H C
Life Sci. 1984 Apr 2;34(14):1379-87. doi: 10.1016/0024-3205(84)90010-9.
The effects of severe global ischemia on cardiac high energy phosphate (HEP) stores were investigated in an in vitro rat model. The heart was removed from the rat in this model, sealed in a plastic bag and incubated for varying times and temperatures (20-45 degrees C). The rat, in the in vivo anoxic model, was subjected to cervical dislocation which resulted in respiratory arrest. In both models the hearts were removed and analyzed for HEP at appropriate times following the onset of anoxia or ischemia. Verapamil and nifedipine, administered intravenously 10 minutes before the start of the experiments, preserved HEP stores in both models. The degree of protection provided by the Ca+2 blockers was related to both the dose of drug and the duration of the ischemia/anoxia. Verapamil was more active than nifedipine in both models.
在体外大鼠模型中研究了严重全身性缺血对心脏高能磷酸酯(HEP)储备的影响。在此模型中,将大鼠心脏取出,密封于塑料袋中,并在不同时间和温度(20 - 45摄氏度)下孵育。在体内缺氧模型中,对大鼠进行颈椎脱臼导致呼吸停止。在这两种模型中,缺氧或缺血发作后在适当时间取出心脏并分析HEP。在实验开始前10分钟静脉注射维拉帕米和硝苯地平,在两种模型中均能保留HEP储备。钙通道阻滞剂提供的保护程度与药物剂量和缺血/缺氧持续时间均有关。在两种模型中,维拉帕米比硝苯地平更有效。