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哌唑嗪和普萘洛尔对高血压患者脂蛋白的影响。

Effect of prazosin and propranolol on lipoproteins of hypertensive patients.

作者信息

Hurt E, Velasco M, Silva H, Camejo G

出版信息

Biomed Biochim Acta. 1987;46(1):111-8.

PMID:3107546
Abstract

A comparative study between prazosin and propranolol with twenty male patients with mild to moderate essential hypertension was used to study the effects of these antihypertensive agents on plasma lipoproteins, and more specifically high density lipoproteins-2 and Apo A-I. After 4 weeks on placebo, the patients were randomly assigned to prazosin therapy (Group A) and other ten patients to propranolol therapy (Group B) for 8 weeks. Doses required for normalization of blood pressure ranged between 1 to 8 mg/day for prazosin and 20 to 240 mg/day for propranolol. The mean blood pressure was lowered to normal by both drugs. The results indicate that prazosin has no adverse effects on plasma lipids and lipoproteins separated by density gradient centrifugation. In contrast, propranolol increased total plasma triglycerides and decreased high density lipoprotein-2 apoprotein A-I and cholesterol levels by 50% in the group of ten patients. Since low levels of high density lipoproteins have been found to be associated with an increased incidence of coronary artery disease, the data obtained suggest that propranolol may induce significant, potentially atherogenic changes on lipid metabolism in hypertensive patients.

摘要

一项针对20名轻度至中度原发性高血压男性患者的哌唑嗪与普萘洛尔的对比研究,旨在探究这些抗高血压药物对血浆脂蛋白,尤其是高密度脂蛋白-2和载脂蛋白A-I的影响。在服用安慰剂4周后,患者被随机分为两组,10名患者接受哌唑嗪治疗(A组),另外10名患者接受普萘洛尔治疗(B组),为期8周。使血压恢复正常所需的剂量,哌唑嗪为每日1至8毫克,普萘洛尔为每日20至240毫克。两种药物均能使平均血压降至正常水平。结果表明,哌唑嗪对通过密度梯度离心分离的血浆脂质和脂蛋白没有不良影响。相比之下,在10名患者组成的B组中,普萘洛尔使血浆总甘油三酯升高,高密度脂蛋白-2载脂蛋白A-I和胆固醇水平降低了50%。由于已发现高密度脂蛋白水平较低与冠状动脉疾病发病率增加有关,所得数据表明普萘洛尔可能会在高血压患者的脂质代谢中引发显著的、潜在的致动脉粥样硬化变化。

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