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选择性α1和β1肾上腺素能受体阻滞剂对高血压患者脂蛋白和碳水化合物代谢的影响,特别关注胰岛素敏感性。

Effects of selective alfa 1 and beta 1-adrenoreceptor blockade on lipoprotein and carbohydrate metabolism in hypertensive subjects, with special emphasis on insulin sensitivity.

作者信息

Andersson P E, Johansson J, Berne C, Lithell H

机构信息

Department of Geriatrics, Kungsgärdets Hospital, Uppsala, Sweden.

出版信息

J Hum Hypertens. 1994 Mar;8(3):219-26.

PMID:8006923
Abstract

The central role of insulin resistance in patients with essential hypertension was the impetus for the present study, in which carbohydrate and lipid metabolism were examined before and after three months treatment with doxazosin (n = 14) and atenolol (n = 15). After completion of a randomised parallel group trial, the study was extended in a subgroup of the patients who continued treatment with doxazosin for a further nine months (n = 18). Insulin sensitivity was measured with the euglycemic hyperinsulinaemic clamp. Blood glucose and plasma insulin were analysed in the fasting state and during an intravenous glucose tolerance test (IVGTT). Lipoprotein fractions were analysed in serum. After three months, SBP and DBP in the standing position decreased to the same extent after the two drugs whereas the decrease in supine SBP did not reach statistical significance in the doxazosin group. Doxazosin, in contrast to atenolol, decreased serum triglycerides (-17%, P < 0.04) by lowering the VLDL and LDL fractions. Serum cholesterol fell after doxazosin (-7%, P < 0.02) but not after atenolol. The effects of doxazosin on serum lipids remained the same during the long-term follow-up. At three months neither drug had significantly affected variables reflecting insulin sensitivity although atenolol tended to decrease the insulin sensitivity index (-17%, P = 0.08). After 12 months the doxazosin group showed a significant increase in the insulin sensitivity index and a significant decrease in both basal plasma insulin and in the late insulin response at IVGTT.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

胰岛素抵抗在原发性高血压患者中的核心作用是本研究的动力,本研究对14例服用多沙唑嗪和15例服用阿替洛尔的患者在治疗三个月前后的碳水化合物和脂质代谢进行了检查。在完成随机平行组试验后,对继续服用多沙唑嗪九个月的患者亚组(n = 18)进行了研究扩展。采用正常血糖高胰岛素钳夹技术测量胰岛素敏感性。在空腹状态和静脉葡萄糖耐量试验(IVGTT)期间分析血糖和血浆胰岛素。分析血清中的脂蛋白组分。三个月后,两种药物使站立位收缩压(SBP)和舒张压(DBP)下降程度相同,而多沙唑嗪组仰卧位SBP的下降未达到统计学意义。与阿替洛尔相比,多沙唑嗪通过降低极低密度脂蛋白(VLDL)和低密度脂蛋白(LDL)组分降低血清甘油三酯(-17%,P < 0.04)。多沙唑嗪治疗后血清胆固醇下降(-7%,P < 0.02),而阿替洛尔治疗后未下降。多沙唑嗪对血清脂质的影响在长期随访中保持不变。三个月时,两种药物均未显著影响反映胰岛素敏感性的指标,尽管阿替洛尔有降低胰岛素敏感性指数的趋势(-17%,P = 0.08)。12个月后,多沙唑嗪组胰岛素敏感性指数显著升高,基础血浆胰岛素和IVGTT后期胰岛素反应均显著降低。(摘要截短于250字)

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引用本文的文献

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Metabolic effects of long-term angiotensin-converting enzyme inhibition with fosinopril in patients with essential hypertension: relationship to angiotensin-converting enzyme inhibition.福辛普利长期抑制血管紧张素转换酶对原发性高血压患者的代谢影响:与血管紧张素转换酶抑制的关系
Eur J Clin Pharmacol. 1994;46(5):431-6. doi: 10.1007/BF00191906.
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Doxazosin. An update of its clinical pharmacology and therapeutic applications in hypertension and benign prostatic hyperplasia.多沙唑嗪。其临床药理学及在高血压和良性前列腺增生症治疗应用方面的最新进展。
Drugs. 1995 Feb;49(2):295-320. doi: 10.2165/00003495-199549020-00011.