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门静脉内高胰岛素血症会降低犬体内胰岛素刺激的葡萄糖摄取。

Intraportal hyperinsulinemia decreases insulin-stimulated glucose uptake in the dog.

作者信息

McGuinness O P, Friedman A, Cherrington A D

机构信息

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

出版信息

Metabolism. 1990 Feb;39(2):127-32. doi: 10.1016/0026-0495(90)90064-j.

Abstract

Hyperinsulinemia and insulin resistance are commonly seen in obese and non-insulin-dependent diabetes mellitis (NIDDM) patients. While it is known that chronic exposure to severe hyperinsulinemia can lead to an insulin-resistant state and mild hyperinsulinemia for rather short durations (20 to 40 hours) and can also lead to insulin resistance, it is less clear whether mild hyperinsulinemia for a more prolonged duration can lead to insulin resistance. In the present study we determined the effects of chronic (28 days) exposure to mild hyperinsulinemia on insulin-stimulated glucose use. Chronic hyperinsulinemia was produced by an intraportal infusion of porcine insulin (425 microU/kg/min), which raised the basal peripheral insulin levels by approximately 50%. Insulin responsiveness was assessed using the euglycemic hyperinsulinemic clamp (2 mU/kg/min) in dogs before the induction of chronic hyperinsulinemia (day 0), after 28 days of hyperinsulinemia (day 28), and 28 days after discontinuation of the chronic insulin infusion (day 56). The amount of glucose (M) required to maintain euglycemia during the euglycemic hyperinsulinemic clamp was decreased (relative to day 0) 39% +/- 3% on day 28 and 18% +/- 3% on day 56 (P less than .05). In control animals that received a chronic infusion of saline for the 28-day period the glucose infusion rate (M) was not changed significantly (decreasing 2% +/- 5% and 5% +/- 10% on days 28 and 56, respectively). In conclusion insulin resistance can be produced by a mild hypersecretion of insulin and discontinuation of the chronic insulin infusion tends to reverse the resistance.

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。虽然已知长期暴露于严重的高胰岛素血症会导致胰岛素抵抗状态,而短期(20至40小时)的轻度高胰岛素血症也会导致胰岛素抵抗,但对于持续时间更长的轻度高胰岛素血症是否会导致胰岛素抵抗尚不清楚。在本研究中,我们确定了长期(28天)暴露于轻度高胰岛素血症对胰岛素刺激的葡萄糖利用的影响。通过门静脉内输注猪胰岛素(425微单位/千克/分钟)产生慢性高胰岛素血症,这使基础外周胰岛素水平提高了约50%。在诱导慢性高胰岛素血症前(第0天)、高胰岛素血症28天后(第28天)以及停止慢性胰岛素输注28天后(第56天),使用正常血糖高胰岛素钳夹技术(2毫单位/千克/分钟)评估犬的胰岛素反应性。在正常血糖高胰岛素钳夹期间维持正常血糖所需的葡萄糖量(M)在第28天相对于第0天降低了39%±3%,在第56天降低了18%±3%(P<0.05)。在接受为期28天生理盐水慢性输注的对照动物中,葡萄糖输注速率(M)没有显著变化(分别在第28天和第56天降低了2%±5%和5%±10%)。总之,胰岛素轻度分泌过多可导致胰岛素抵抗,停止慢性胰岛素输注往往会使这种抵抗逆转。

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