Larsson R, Karlberg B E, Norlander B, Wirsén A
Clin Pharmacol Ther. 1981 May;29(5):588-93. doi: 10.1038/clpt.1981.82.
Single oral doses of 1.5, 3.0, 4.5 and 6.0 mg/kg prizidilol HCl, an antihypertensive with vasodilator and beta-adrenoceptor blocking actions, were given to 12 patients with primary hypertension on separate days. Systolic and diastolic blood pressure (BP) decreased after 4.5 and 6.0 mg/kg and systolic BP also after 3.0 mg/kg. The antihypertensive effect was evident in 1 to 2 hr with maximum effect in 4 to 5 hr (supine systolic BP 20 and diastolic 13 mm Hg after 6.0 mg/kg); the effect was sustained for more than 8 hr. An initial slight reduction in heart rate (HR) after 1 to 2 hr was followed by a slight rise after 6 to 8 hr. There were higher plasma drug levels and greater antihypertensive effects after the 6.0-mg/kg dose in slow acetylators (n = 5) than in rapid acetylators (n = 7). Due to its hydrazine moiety, prizidilol, like hydralazine, seems to be a substrate for the polymorphic N-acetyltransferase enzyme system.
对12例原发性高血压患者在不同日期分别单次口服1.5、3.0、4.5和6.0mg/kg的盐酸普齐地洛,这是一种具有血管舒张和β-肾上腺素能受体阻断作用的抗高血压药。4.5mg/kg和6.0mg/kg剂量后收缩压和舒张压下降,3.0mg/kg剂量后收缩压也下降。降压作用在1至2小时内明显,4至5小时达到最大效应(6.0mg/kg后仰卧位收缩压下降20mmHg,舒张压下降13mmHg);该效应持续超过8小时。心率在1至2小时后最初略有下降,随后在6至8小时后略有上升。慢乙酰化者(n = 5)服用6.0mg/kg剂量后的血浆药物水平更高,降压效果也比快乙酰化者(n = 7)更显著。由于其肼基部分,普齐地洛与肼屈嗪一样,似乎是多态性N-乙酰转移酶系统的底物。