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慢性高胰岛素血症会降低胰岛素作用,但不会降低胰岛素敏感性。

Chronic hyperinsulinemia decreases insulin action but not insulin sensitivity.

作者信息

McGuinness O P, Myers S R, Neal D, Cherrington A D

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN 37232.

出版信息

Metabolism. 1990 Sep;39(9):931-7. doi: 10.1016/0026-0495(90)90303-t.

Abstract

Hyperinsulinemia and insulin resistance are commonly seen in obese and non-insulin-dependent diabetes mellitus (NIDDM) patients, suggesting a causal link exists between hyperinsulinemia and insulin resistance. In a previous study, we demonstrated that chronic (28 days) intraportal hyperinsulinemia (50% increase in basal insulin levels) resulted in a decrease in insulin action as assessed by a one-step euglycemic hyperinsulinemic clamp. Since only one dose of insulin was used during the clamp, it was not possible to determine if the decrease in insulin action was due to a change in insulin sensitivity and/or maximal insulin responsiveness. In the present study, insulin resistance was induced as before, but insulin action was assessed in overnight fasted conscious dogs using a four-step euglycemic hyperinsulinemic clamp (1, 2, 10, and 15 mU/kg/min). Insulin responsiveness was assessed before the induction of chronic hyperinsulinemia (day 0), and after 28 days of hyperinsulinemia (day 28). Transhepatic glucose balance and whole-body glucose utilization were measured to allow assessment of both the hepatic and peripheral effects of insulin. Chronic hyperinsulinemia increased basal insulin levels from 13 +/- 2 to 21 +/- 4 microU/mL. After 4 weeks of chronic hyperinsulinemia, maximal insulin-stimulated glucose utilization was decreased 23% +/- 4% (P less than .05) and insulin sensitivity (ED50) was not significantly altered. During the four-step clamp, the liver was a major site of glucose utilization. The liver was responsible for 13% of the total glucose disposal rate on day 0 (2.9 mg/kg/min) at the highest insulin infusion rate (15 mU/kg/min; 2,000 microU/mL).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

高胰岛素血症和胰岛素抵抗常见于肥胖及非胰岛素依赖型糖尿病(NIDDM)患者中,这表明高胰岛素血症与胰岛素抵抗之间存在因果联系。在之前的一项研究中,我们证明,通过一步法正常血糖高胰岛素钳夹试验评估,慢性(28天)门静脉内高胰岛素血症(基础胰岛素水平增加50%)会导致胰岛素作用降低。由于在钳夹试验期间仅使用了一剂胰岛素,因此无法确定胰岛素作用的降低是由于胰岛素敏感性变化和/或最大胰岛素反应性变化所致。在本研究中,像之前一样诱导胰岛素抵抗,但在过夜禁食的清醒犬中使用四步法正常血糖高胰岛素钳夹试验(1、2、10和15 mU/kg/分钟)评估胰岛素作用。在诱导慢性高胰岛素血症之前(第0天)和高胰岛素血症28天后(第28天)评估胰岛素反应性。测量经肝葡萄糖平衡和全身葡萄糖利用情况,以评估胰岛素的肝脏和外周效应。慢性高胰岛素血症使基础胰岛素水平从13±2微U/mL增至21±4微U/mL。慢性高胰岛素血症4周后,最大胰岛素刺激的葡萄糖利用率降低了23%±4%(P<0.05),胰岛素敏感性(ED50)未显著改变。在四步法钳夹试验期间,肝脏是葡萄糖利用的主要部位。在第0天,当胰岛素输注速率最高(15 mU/kg/分钟;2,000微U/mL)时,肝脏占总葡萄糖处置率的13%(2.9 mg/kg/分钟)。(摘要截选至250词)

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