Choong C Y, Roubin G S, Harris P J, Tokuyasu Y, Shen W F, Bautovich G J, Kelly D T
J Cardiovasc Pharmacol. 1986 May-Jun;8(3):441-8. doi: 10.1097/00005344-198605000-00001.
The effects on hemodynamics and left ventricular function of propranolol and pindolol, beta-blockers without and with intrinsic sympathomimetic activity (ISA), respectively, were compared in six men with stable exertional angina at rest and during symptom-limited bicycle exercise. The study was controlled and double blinded, and the order of drug administration was randomized. The dosage of each drug (propranolol 0.15 mg/kg i.v., pindolol 0.02 mg/kg i.v.) was chosen to reduce exercise tachycardia by approximately 18%. Exercise capacity and duration were similar after each drug, and both drugs similarly reduced ST depression during exercise. At rest, propranolol significantly reduced heart rate, systolic arterial pressure, rate-pressure product, stroke volume index, cardiac index, and left ventricular ejection fraction, and increased systemic vascular resistance. In contrast, pindolol significantly reduced only the rate-pressure product and cardiac index, and to a lesser extent than propranolol. During exercise on the other hand, both drugs reduced the heart rate, arterial pressure, rate-pressure product, and cardiac index to a similar degree. Neither drug altered pulmonary artery wedge pressure, systemic vascular resistance, stroke volume index, left ventricular ejection fraction, or left ventricular end-diastolic and end-systolic volume indices. At equipotent beta-blocking dosages, ISA in pindolol reduced the effects of beta-blockade on resting hemodynamics and left ventricular function compared to propranolol, but during exercise the influence of ISA was reduced; and both pindolol and propranolol exert similar effects on hemodynamics and left ventricular function.
分别比较了无内在拟交感活性(ISA)的普萘洛尔和有ISA的吲哚洛尔对6名稳定型劳力性心绞痛男性患者静息时和症状限制性自行车运动期间血流动力学及左心室功能的影响。该研究为对照双盲试验,药物给药顺序随机。选择每种药物的剂量(普萘洛尔0.15mg/kg静脉注射,吲哚洛尔0.02mg/kg静脉注射)以将运动性心动过速降低约18%。每种药物给药后运动能力和持续时间相似,且两种药物在运动期间均同样程度地减少ST段压低。静息时,普萘洛尔显著降低心率、收缩期动脉压、心率-血压乘积、每搏量指数、心脏指数和左心室射血分数,并增加全身血管阻力。相比之下,吲哚洛尔仅显著降低心率-血压乘积和心脏指数,且程度小于普萘洛尔。另一方面,在运动期间,两种药物均将心率、动脉压、心率-血压乘积和心脏指数降低至相似程度。两种药物均未改变肺动脉楔压、全身血管阻力、每搏量指数、左心室射血分数或左心室舒张末期和收缩末期容积指数。在等效的β受体阻滞剂剂量下,与普萘洛尔相比,吲哚洛尔中的ISA降低了β受体阻滞剂对静息血流动力学和左心室功能的影响,但在运动期间ISA的影响减弱;吲哚洛尔和普萘洛尔对血流动力学和左心室功能均产生相似的影响。