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α受体阻滞剂和选择性β受体阻滞剂控制高血压对血浆脂蛋白、载脂蛋白、脂蛋白亚类及餐后血脂的影响。

Effect of alpha- and selective beta-blockade for hypertension control on plasma lipoproteins, apoproteins, lipoprotein subclasses, and postprandial lipemia.

作者信息

Superko H R, Wood P D, Krauss R M

机构信息

Stanford Center for Research in Disease Prevention, Stanford University School of Medicine, California.

出版信息

Am J Med. 1989 Jan 23;86(1B):26-31. doi: 10.1016/0002-9343(89)90125-3.

Abstract

Fourteen male patients (mean age +/- SD, 52 +/- 11 years) with a history of hypertension (systolic blood pressure, 148 +/- 10 mm Hg; diastolic blood pressure, 99 +/- 2 mm Hg) were enrolled in a cross-over trial of prazosin and atenolol, with a minimum of eight weeks of treatment with each drug. Measures of lipoprotein metabolism included levels of: total plasma cholesterol, triglycerides, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and high-density lipoprotein2 cholesterol. Lipoprotein mass was measured by analytical ultracentrifugation in low-density to very low-density lipoprotein flotation rate intervals of 0 to 12, 12 to 20, and 20 to 400, and high-density lipoprotein flotation rate intervals of 0 to 3.5 and 3.5 to 9.0. Apolipoproteins A1 and B, postheparin lipoprotein and hepatic lipase activities, and magnitude of postprandial lipemia also were determined. Mass of intermediate-density lipoproteins (flotation rate, 12 to 20) was significantly lower (p = 0.05) following prazosin therapy compared with atenolol therapy. Other lipid parameters, including triglycerides and low- and high-density lipoprotein cholesterol, were not significantly different for the two drug treatments.

摘要

14名有高血压病史(收缩压148±10mmHg;舒张压99±2mmHg)的男性患者(平均年龄±标准差,52±11岁)参与了一项哌唑嗪和阿替洛尔的交叉试验,每种药物至少治疗8周。脂蛋白代谢指标包括:血浆总胆固醇、甘油三酯、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇和高密度脂蛋白2胆固醇水平。通过分析超速离心法在低密度至极低密度脂蛋白漂浮率区间0至12、12至20和20至400以及高密度脂蛋白漂浮率区间0至3.5和3.5至9.0测量脂蛋白质量。还测定了载脂蛋白A1和B、肝素后脂蛋白和肝脂酶活性以及餐后血脂水平。与阿替洛尔治疗相比,哌唑嗪治疗后中密度脂蛋白(漂浮率12至20)质量显著降低(p=0.05)。两种药物治疗的其他脂质参数,包括甘油三酯以及低密度和高密度脂蛋白胆固醇,没有显著差异。

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