Rönn O, Johnsson G, Lundborg P
J Cardiovasc Pharmacol. 1981 May-Jun;3(3):477-84. doi: 10.1097/00005344-198105000-00007.
We studied the hemodynamic effects of the selective beta 1-adrenoceptor agonist prenalterol in healthy subjects before and after intravenous infusion of the nonselective beta-adrenoceptor blocker propranolol or the beta 1-selective adrenoceptor blocker metoprolol. Intravenous infusions of 0.1, 0.25, and 0.5 mg prenalterol induced a dose-dependent decrease in total electromechanical systole and pre-injection period, whereas left ventricular ejection time remained unchanged. Stoke volume as determined by impedance cardiography was not changed, but a dose-dependent increase in cardiac output due to an increase in heart rate was observed. Systolic blood pressure was significantly increased, but diastolic blood pressure remained unchanged. After intravenous administration of either 10 mg propranolol or 20 mg metoprolol, prenalterol was infused in a 10 times higher dose than before. The hemodynamic effects were similar to those observed before the beta-blockers. Whether propranolol or metoprolol was administered did not influence the effects induced by prenalterol. It is suggested that prenalterol might be a useful drug to counteract undesired hemodynamic effects of beta-adrenoceptor blockers.
我们研究了在健康受试者静脉输注非选择性β肾上腺素能受体阻滞剂普萘洛尔或β1选择性肾上腺素能受体阻滞剂美托洛尔之前和之后,选择性β1肾上腺素能受体激动剂普瑞特罗的血流动力学效应。静脉输注0.1、0.25和0.5毫克普瑞特罗可导致总机电收缩期和注射前期呈剂量依赖性缩短,而左心室射血时间保持不变。通过阻抗心动图测定的每搏输出量未改变,但由于心率增加,观察到心输出量呈剂量依赖性增加。收缩压显著升高,但舒张压保持不变。静脉注射10毫克普萘洛尔或20毫克美托洛尔后,以比之前高10倍的剂量输注普瑞特罗。血流动力学效应与β受体阻滞剂给药前观察到的效应相似。给予普萘洛尔还是美托洛尔并不影响普瑞特罗诱导的效应。提示普瑞特罗可能是一种有用的药物,可抵消β肾上腺素能受体阻滞剂不良的血流动力学效应。