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原发性高血压中的α-1肾上腺素能阻断与脂蛋白代谢

Alpha-1-adrenergic blockade and lipoprotein metabolism in essential hypertension.

作者信息

Ferrier C, Beretta-Piccoli C, Weidmann P, Mordasini R

出版信息

Clin Pharmacol Ther. 1986 Nov;40(5):525-30. doi: 10.1038/clpt.1986.218.

Abstract

The effect of the selective alpha 1-antagonist terazosin on serum lipoproteins and certain blood pressure-regulating factors was assessed in 15 patients with essential hypertension. Terazosin given during 8 weeks reduced arterial pressure (from 153/103 +/- 3/2 (SE) to 143/96 +/- 5/2 mm Hg; P less than 0.02) but did not modify body weight, heart rate, blood volume, plasma renin activity, aldosterone and catecholamine levels, or serum cholesterol, triglycerides, and their lipoprotein fractions. In nine of the patients, blood pressure control was not achieved with terazosin monotherapy and the diuretic methyclothiazide, 2.5 mg, was added. After 8 weeks of combined treatment, blood pressure decreased further (P less than 0.05); serum lipids and lipoprotein fractions did not change as compared with placebo or terazosin conditions. These findings indicate that terazosin in monotherapy does not unfavorably influence lipid metabolism.

摘要

在15例原发性高血压患者中评估了选择性α1拮抗剂特拉唑嗪对血清脂蛋白及某些血压调节因子的影响。在8周期间给予特拉唑嗪可降低动脉压(从153/103±3/2(标准误)降至143/96±5/2 mmHg;P<0.02),但未改变体重、心率、血容量、血浆肾素活性、醛固酮及儿茶酚胺水平,或血清胆固醇、甘油三酯及其脂蛋白组分。在9例患者中,单用特拉唑嗪未实现血压控制,遂加用2.5 mg利尿药甲氯噻嗪。联合治疗8周后,血压进一步下降(P<0.05);与安慰剂或特拉唑嗪治疗情况相比,血清脂质及脂蛋白组分未发生变化。这些发现表明,单用特拉唑嗪不会对脂质代谢产生不利影响。

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