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钙拮抗剂对原发性高血压的急性降压及激素效应

Acute antihypertensive and hormonal effects of a calcium antagonist in essential hypertension.

作者信息

Thibonnier M, Corvol P, Banzet O, Menard J

出版信息

J Cardiovasc Pharmacol. 1982;4 Suppl 3:S335-9.

PMID:6184564
Abstract

In a double-blind versus placebo preliminary study conducted in seven mildly hypertensive patients, the 10-mg capsule form of nifedipine was able to reduce significantly systolic and diastolic blood pressure (-14%) for 3 h. In a single-dose, cross-over study, captopril (1 mg/kg) and nifedipine (20 mg) significantly reduced blood pressure in 12 patients with moderate essential hypertension, but the mean maximum arterial pressure reduction was faster and greater with nifedipine than with captopril (-23 +/- 2% at 37 +/- 15 min and -17 +/- 1% at 86 +/- 25 min, respectively). Nifedipine did not significantly alter the renin angiotensin aldosterone system in supine and upright positions, and the blood pressure drop it induced was not related to the initial level of activation of that system. Associated with the stimulation of the sympathetic nervous system, an increased release of vasopressin was noted during nifedipine administration. Finally, nifedipine, a calcium antagonist, was a potent antihypertensive drug through its vasodilating properties. It provoked specific hormonal alterations, i.e., stimulation of catecholamines and vasopressin release, whereas the renin angiotensin aldosterone system was not significantly altered.

摘要

在一项针对7名轻度高血压患者进行的双盲对照安慰剂初步研究中,10毫克胶囊剂型的硝苯地平能够在3小时内显著降低收缩压和舒张压(降低14%)。在一项单剂量交叉研究中,卡托普利(1毫克/千克)和硝苯地平(20毫克)使12名中度原发性高血压患者的血压显著降低,但硝苯地平使平均最大动脉压降低的速度更快、幅度更大,分别在37±15分钟时降低23±2%,在86±25分钟时降低17±1%。硝苯地平在仰卧位和直立位时并未显著改变肾素 - 血管紧张素 - 醛固酮系统,其引起的血压下降与该系统的初始激活水平无关。在硝苯地平给药期间,伴随着交感神经系统的刺激,观察到血管加压素释放增加。最后,硝苯地平作为一种钙拮抗剂,通过其血管舒张特性成为一种有效的降压药物。它引发了特定的激素变化,即刺激儿茶酚胺和血管加压素释放,而肾素 - 血管紧张素 - 醛固酮系统并未显著改变。

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