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血管紧张素转换酶抑制剂、钙通道拮抗剂及α-肾上腺素能阻滞剂对非胰岛素依赖型糖尿病合并高血压患者糖脂代谢的影响

Effects of angiotensin-converting enzyme inhibitors, Ca2+ channel antagonists, and alpha-adrenergic blockers on glucose and lipid metabolism in NIDDM patients with hypertension.

作者信息

Giordano M, Matsuda M, Sanders L, Canessa M L, DeFronzo R A

机构信息

Department of Medicine, University of Texas Health Sciences Center, San Antonio 78284-7886, USA.

出版信息

Diabetes. 1995 Jun;44(6):665-71. doi: 10.2337/diab.44.6.665.

Abstract

We compared the effects of captopril, nifedipine, and doxazosin on glucose and lipid metabolism in 30 hypertensive non-insulin-dependent diabetes mellitus (NIDDM) patients (age = 50 +/- 3 years; body mass index = 30 +/- 1 kg/m2). Of these patients, 9 were treated with captopril, 11 with nifedipine, and 10 with doxazosin for 12 weeks. Blood pressure, fasting plasma glucose (FPG) concentration, HbA1c, oral glucose tolerance test (OGTT), euglycemic insulin clamp, and plasma lipids were measured before and after a 3-month period. Mean arterial blood pressure (114 +/- 2 mmHg) was similar in all groups before initiating antihypertensive therapy and declined to 102 +/- 2 (captopril), 103 +/- 1 (nifedipine), and 103 +/- 2 (doxazosin) mmHg (P < 0.001). Baseline FPG (148 +/- 11 mg/dl) and HbA1c (6.3 +/- 1%) were similar in all groups and did not change significantly with treatment. Plasma glucose, insulin, and free fatty acid (FFA) concentrations during the OGTT were similar in all groups before antihypertensive treatment and did not change with captopril and nifedipine; after doxazosin, plasma glucose and FFA concentrations during the OGTT decreased (both P < 0.05) without change in plasma insulin response. Insulin-mediated glucose uptake (144 +/- 11 mg.m-2.min-1), glucose oxidation (76 +/- 4 mg.m-2.min-1), and nonoxidative glucose disposal (71 +/- 6 mg.m-2.min-1) were similar in all groups before the start of antihypertensive treatment and did not change in captopril and nifedipine groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们比较了卡托普利、硝苯地平和多沙唑嗪对30例高血压非胰岛素依赖型糖尿病(NIDDM)患者(年龄=50±3岁;体重指数=30±1kg/m²)糖脂代谢的影响。这些患者中,9例接受卡托普利治疗,11例接受硝苯地平治疗,10例接受多沙唑嗪治疗,为期12周。在3个月疗程前后测量血压、空腹血糖(FPG)浓度、糖化血红蛋白(HbA1c)、口服葡萄糖耐量试验(OGTT)、正常血糖胰岛素钳夹试验及血脂。在开始抗高血压治疗前,所有组的平均动脉血压(114±2mmHg)相似,治疗后分别降至102±2(卡托普利)、103±1(硝苯地平)和103±2(多沙唑嗪)mmHg(P<0.001)。所有组的基线FPG(148±11mg/dl)和HbA1c(6.3±1%)相似,治疗后无显著变化。在抗高血压治疗前,所有组OGTT期间的血糖、胰岛素和游离脂肪酸(FFA)浓度相似,卡托普利和硝苯地平治疗后无变化;多沙唑嗪治疗后,OGTT期间的血糖和FFA浓度降低(均P<0.05),血浆胰岛素反应无变化。在开始抗高血压治疗前,所有组的胰岛素介导的葡萄糖摄取(144±11mg·m⁻²·min⁻¹)、葡萄糖氧化(76±4mg·m⁻²·min⁻¹)和非氧化葡萄糖处置(71±6mg·m⁻²·min⁻¹)相似,卡托普利和硝苯地平组无变化。(摘要截断于250字)

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