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普瑞地洛对原发性高血压患者血压、心率、儿茶酚胺、肾素和醛固酮的急性影响。

Acute effects of prizidilol on blood pressure, heart rate, catecholamines, renin and aldosterone in essential hypertension.

作者信息

Bianchetti M G, Boehringer K, Weidmann P, Link L, Schiffl H, Ziegler W H

出版信息

Eur J Clin Pharmacol. 1982 Oct;23(4):289-96. doi: 10.1007/BF00613608.

Abstract

Prizidilol is a new antihypertensive agent reported to possess combined precapillary vasodilator and betareceptor-blocking properties. To clarify the profile of the acute effects of prizidilol in man, a variable dose study was performed in 8 patients with benign essential hypertension. Blood pressure, heart rate, plasma renin activity, aldosterone, plasma and urinary catecholamines and electrolytes were determined at short intervals before and up to 23 h after oral administration of placebo and prizidilol 150, 300 and 600 mg. The 4 studies were performed at weekly intervals according to a Latin square design. Prizidilol produced dose-dependent decreases in supine and upright blood pressure, with an initial change after about 2 h and maximal effects from 4 to 8 h after drug ingestion. Following a high dose of prizidilol, supine mean blood pressure (average 128 mmHg prior to treatment) was normalised (less than 107 mmHg) from 3 to 7 h and was still below predose level 23 h after ingestion. The only reported side effects were postural dizziness in 2 cases (corresponding to a fall in systolic upright blood pressure to less than 95 mmHg) and headache in one case. A biphasic variation in heart rate and plasma renin activity, with an early drop and a subsequent tendency to a slight rise, was observed after an intermediate or high dose of prizidilol. Plasma norepinephrine levels were increased by a high dose of prizidilol, while plasma epinephrine, aldosterone and plasma and urinary electrolytes were not consistently changed. Prizidilol in a a single oral dose appeared to be a potent antihypertensive agent. The profile of heart rate and plasma renin point to early dominance of beta-blockade followed by appearance of the concomitant vasodilator properties of prizidiol.

摘要

普齐地洛是一种新的抗高血压药物,据报道它具有毛细血管前血管扩张剂和β受体阻断剂的联合特性。为了阐明普齐地洛对人体的急性作用特征,对8例良性原发性高血压患者进行了可变剂量研究。在口服安慰剂和150、300和600毫克普齐地洛之前及之后长达23小时的短时间间隔内,测定血压、心率、血浆肾素活性、醛固酮、血浆和尿儿茶酚胺以及电解质。这4项研究按照拉丁方设计每周进行一次。普齐地洛可使仰卧位和直立位血压呈剂量依赖性下降,服药后约2小时开始出现初始变化,4至8小时达到最大效果。服用高剂量普齐地洛后,仰卧位平均血压(治疗前平均为128 mmHg)在3至7小时恢复正常(低于107 mmHg),服药后23小时仍低于服药前水平。唯一报告的副作用是2例出现体位性头晕(对应于直立位收缩压降至低于95 mmHg)和1例头痛。服用中等剂量或高剂量普齐地洛后,观察到心率和血浆肾素活性呈双相变化,早期下降,随后有轻微上升的趋势。高剂量普齐地洛可使血浆去甲肾上腺素水平升高,而血浆肾上腺素、醛固酮以及血浆和尿电解质未见持续变化。单次口服普齐地洛似乎是一种有效的抗高血压药物。心率和血浆肾素的变化特征表明,早期以β受体阻断作用为主,随后出现普齐地洛的血管扩张剂特性。

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