Waal-Manning H J
N Z Med J. 1976 Apr 14;83(561):223-6.
The antihypertensive and pulse-slowing effects of racemic propranolol, oxprenolol, pindolol, practolol and d-propranolol were assessed in 54 hypertensive patients. Drug dosage was selected to be proportionate to beta-adrenoreceptor-blocking potency; d-propranolol dosage equalled approximately that of racemic propranolol. D-propranolol had onlyslight antihypertensive effect; the four other drugs were found to have a considerable and approximately equal antihypertensive effect. The degree of slowing of heart rate varied with the different drugs, being greatest with racemic propanolol. The effect on pulse rate did not correlate with the effect on blood pressure for most of the drugs. The falls in blood pressure induced by racemic propanolol were strongly correlated with those induced by each of the other drugs. The small falls in blood pressured induced by d-propranolol correlated also with those induced by practolol (which had no membrane activity) and are presumably due to its weak beta-adrenoreceptor-blocking action. The beta-adrenoreceptor-blocking action per se is responsible for the antihypertensive action of these drugs.
在54例高血压患者中评估了消旋普萘洛尔、氧烯洛尔、吲哚洛尔、普拉洛尔和d-普萘洛尔的降压及减慢心率作用。药物剂量选择与β-肾上腺素能受体阻断效能成比例;d-普萘洛尔剂量约等于消旋普萘洛尔的剂量。d-普萘洛尔仅有轻微的降压作用;发现其他四种药物有相当且大致相等的降压作用。心率减慢程度因药物不同而有所差异,消旋普萘洛尔引起的心率减慢最为明显。大多数药物对脉率的影响与对血压的影响不相关。消旋普萘洛尔引起的血压下降与其他每种药物引起的血压下降密切相关。d-普萘洛尔引起的小幅度血压下降也与普拉洛尔(无膜活性)引起的血压下降相关,推测是由于其较弱的β-肾上腺素能受体阻断作用。这些药物的降压作用本身是由β-肾上腺素能受体阻断作用引起的。