Kingston W J, Livingston J N, Moxley R T
J Clin Invest. 1986 Apr;77(4):1153-62. doi: 10.1172/JCI112416.
Previous investigations in normal humans and rats have shown an increase in insulin sensitivity and binding affinity of adipocytes isolated 1-3 h after glucose ingestion. To determine whether a rapid enhancement of the action of insulin follows glucose ingestion in vivo, the present studies have utilized 120-min 20 mU/m2 X min euglycemic insulin infusions before and after 7.5-, 15-, 25-, and 100-g oral glucose loads. Euglycemic insulin infusions after the carbohydrate challenge were begun after arterialized blood glucose and insulin values had returned to baseline. After 15- and 25-g oral glucose loads during the 20-120-min interval of insulin infusion, glucose infusion rates increased by 44 +/- 6% (P less than 0.0001) and 47 +/- 9% (P less than 0.0002), respectively. No significant differences in arterialized glucose or insulin values existed between basal and post-glucose insulin infusions. In addition, no significant differences in hepatic glucose production or counter-regulatory hormone levels were found between basal and post-glucose insulin infusions. Control infusion studies including subjects who ingested saline or mannitol failed to show an increase in insulin action. Studies were carried out to mimic the insulin curve seen after 15- and 25-g oral glucose loads. Euglycemic insulin infusions after these insulin simulation studies show a 34 +/- 7% enhancement compared to baseline euglycemic insulin infusions. These results demonstrate a rapid enhancement of insulin action after oral glucose challenge in normal humans. The insulin simulation studies suggest that insulin itself either directly or through release of another factor acts on muscle to increase insulin sensitivity. The increase in insulin action demonstrated in these investigations may represent an important regulatory mechanism to modulate tissue insulin sensitivity.
先前对正常人和大鼠的研究表明,在摄入葡萄糖后1 - 3小时分离的脂肪细胞,其胰岛素敏感性和结合亲和力会增加。为了确定在体内摄入葡萄糖后是否会迅速增强胰岛素的作用,本研究在口服7.5克、15克、25克和100克葡萄糖负荷前后,进行了120分钟、20 mU/m²×分钟的正常血糖胰岛素输注。在碳水化合物激发后进行正常血糖胰岛素输注,是在动脉化血糖和胰岛素值恢复到基线后开始的。在胰岛素输注的20 - 120分钟间隔内,口服15克和25克葡萄糖负荷后,葡萄糖输注率分别增加了44±6%(P<0.0001)和47±9%(P<0.0002)。基础胰岛素输注和葡萄糖后胰岛素输注之间,动脉化血糖或胰岛素值没有显著差异。此外,基础胰岛素输注和葡萄糖后胰岛素输注之间,肝葡萄糖生成或对抗调节激素水平也没有显著差异。包括摄入盐水或甘露醇的受试者的对照输注研究,未能显示胰岛素作用增加。进行了研究以模拟口服15克和25克葡萄糖负荷后出现的胰岛素曲线。与基线正常血糖胰岛素输注相比,这些胰岛素模拟研究后的正常血糖胰岛素输注显示增强了34±7%。这些结果表明,在正常人体中口服葡萄糖激发后胰岛素作用迅速增强。胰岛素模拟研究表明,胰岛素本身要么直接作用,要么通过释放另一种因子作用于肌肉,以增加胰岛素敏感性。在这些研究中证明的胰岛素作用增加,可能代表了一种调节组织胰岛素敏感性的重要调节机制。