Genovese A, Chiariello M, Cacciapuoti A A, De Alfieri W, Latte S, Condorelli M
Basic Res Cardiol. 1980 Nov-Dec;75(6):757-63. doi: 10.1007/BF01910453.
Male Sprague-Dawley rats (200-220 g) were employed to study the effect of a calcium antagonistic drug on hypoxia-induced myocardial hypertrophy. The hypoxic condition was obtained by exposure of animals to reduced barometric pressure in a hypobaric chamber. The rats, divided in groups, were exposed to acute or chronic intermittent hypoxia (0.42 atmospheres of air for 24 hrs or 0.42 atm for 12 hrs per day for 10 days, respectively). Verapamil (VRP) was given subcutaneously in a total dose of 200 mg/kg/b.w./rat. In hypoxic rats, the drug significantly reduced the values of dry heart weight calculated on the basis of its relationship to total body weight. This phenomenon is probably due to: (1) reduced activation of the contractile system and a thereby resulting decrease in ATP breakdown as a result of blocking of Ca++ inflow into myocardial cells; (2) the effect of Verapamil on hypoxia-induced pulmonary hypertension and/or (3) a direct effect of the drug on the myocardial cell.
选用雄性Sprague-Dawley大鼠(体重200 - 220克)来研究一种钙拮抗药物对缺氧诱导的心肌肥大的影响。通过将动物置于低压舱中使其暴露于降低的气压来制造缺氧条件。将大鼠分组,分别暴露于急性或慢性间歇性缺氧环境(分别为每天在0.42个大气压的空气中暴露24小时或每天在0.42个大气压下暴露12小时,持续10天)。维拉帕米(VRP)以200毫克/千克/体重/大鼠的总剂量皮下注射。在缺氧大鼠中,该药物显著降低了基于心脏干重与总体重的关系计算得出的值。这种现象可能是由于:(1)收缩系统的激活减少,以及由于阻止Ca++流入心肌细胞而导致的ATP分解减少;(2)维拉帕米对缺氧诱导的肺动脉高压的作用和/或(3)该药物对心肌细胞的直接作用。