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美托洛尔在原发性高血压患者中的血药浓度及其对血压、肾上腺素能β受体阻滞和血浆肾素活性的影响。

Plasma levels and effects of metoprolol on blood pressure, adrenergic beta receptor blockade, and plasma renin activity in essential hypertension.

作者信息

von Bahr C, Collste P, Frisk-Holmberg M, Haglund K, Jorfelt L, Orme M, Ostman J, Sjoqvist F

出版信息

Clin Pharmacol Ther. 1976 Aug;20(2):130-7. doi: 10.1002/cpt1976202130.

Abstract

The effects of metoprolol, a selective beta adrenergic receptor antagonist, on blood pressure, beta receptor blockade (antagoinst of isoproterenol and exercise tachycardia), and plasma renin activity (PRA) have been compared with those of placebo in 16 patients with essential hypertension. The dose of metroprolol was 25 mg three times daily for 1 wk and thereafter 100 mg three times daily for 5 wk. The mean decrease in blood pressure during treatment with metoprolol was 24 +/- 3.8 (SEM)/10 +/- 2.1 mm Hg in the lying position and 23 +/- 4.4/9 +/- 3.1 mm Hg after 1 min in the standing position. At a dose of 2.9 to 5.4 mg/kg, steady-state plasma concentrations of metoprolol varied 17-fold (from 20 to 341 ng/ml) between patients and correlated with the interindividual variability in isoproterenol antagonism (r = 0.58, p less than 0.05) and decrease in exercise tachycardia (r = 0.65, p less than 0.01). By contrast, neither of these variables correlated with the dose of metoprolol in mg/kg. Metoprolol decreased PRA by 67 +/- 1.9 and 71 +/- 1.2% in the lying and standing positions, respectively. The decrease in the mean arterial blood pressure in the lying position was significantly correlated to the PRA during the placebo period (r = 0.61, p less than 0.05) but not to the plasma steady-state levels of metoprolol, the degree of beta receptor blockade, and the decrease in PRA.

摘要

在16例原发性高血压患者中,比较了选择性β肾上腺素能受体拮抗剂美托洛尔对血压、β受体阻滞(异丙肾上腺素和运动性心动过速的拮抗剂)以及血浆肾素活性(PRA)的影响与安慰剂的效果。美托洛尔的剂量为每日3次,每次25mg,服用1周,此后每日3次,每次100mg,服用5周。美托洛尔治疗期间,卧位血压平均下降24±3.8(SEM)/10±2.1mmHg,立位1分钟后血压平均下降23±4.4/9±3.1mmHg。在2.9至5.4mg/kg的剂量下,患者之间美托洛尔的稳态血浆浓度变化了17倍(从20至341ng/ml),并与异丙肾上腺素拮抗作用的个体间变异性相关(r = 0.58,p<0.05)以及运动性心动过速的降低相关(r = 0.65,p<0.01)。相比之下,这些变量均与美托洛尔mg/kg剂量无关。美托洛尔使卧位和立位的PRA分别降低67±1.9%和71±1.2%。卧位平均动脉血压的降低与安慰剂期的PRA显著相关(r = 0.61,p<0.05),但与美托洛尔的血浆稳态水平、β受体阻滞程度以及PRA的降低无关。

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