Ferrari R, Bongrani S
G Ital Cardiol. 1979;9(4):411-6.
Experiments were undertaken to determine if some drugs (propranolol, reserpine, verapamil and deslanoside) have an effect on CPK release from hypoxic heart muscle. Hypoxia was induced in isolated Langerdorff perfused rabbit hearts by gassing the perfusate with 95% N2 + 5% CO2. Hypoxic induced damage of the rabbit heart muscle has been quantited in terms of the relase of the intracellular enzymes creatinephosphokinase (CPK) into the extracellular space. Propranolol was either added at the start of the hypoxic perfusion or the rabbit were pretreated with it. Verpamil, dl-propranolol and reserpine provided protection evidenced by a reduction of hypoxic induced CPK release, while lanatoside C and d-propranolol failed to prevent the hypoxic muscle from releasing CPK.
进行实验以确定某些药物(普萘洛尔、利血平、维拉帕米和毛花苷丙)是否对缺氧心肌释放肌酸磷酸激酶(CPK)有影响。通过用95% N₂ + 5% CO₂对灌注液进行通气,在离体Langendorff灌注兔心脏中诱导缺氧。缺氧诱导的兔心肌损伤已根据细胞内酶肌酸磷酸激酶(CPK)释放到细胞外空间的情况进行定量。普萘洛尔要么在缺氧灌注开始时添加,要么对兔子进行预处理。维拉帕米、消旋普萘洛尔和利血平提供了保护,表现为缺氧诱导的CPK释放减少,而毛花苷C和右旋普萘洛尔未能阻止缺氧肌肉释放CPK。