Soman V R, DeFronzo R A
Diabetes. 1980 Feb;29(2):159-63. doi: 10.2337/diab.29.2.159.
To directly examine whether physiologic hyperinsulinemia regulates insulin receptors in normal man, we studied the effect of insulin infusion (employing the euglycemic insulin clamp technique) on 125I-insulin binding to monocytes. In Study I (9 subjects), when the steady-state plasma insulin concentration was raised to approximately 100 muU/ml, insulin binding to monocytes remained unchanged at 1 h, but decreased significantly by 3 h (20%, P less than 0.01) and fell further by 5 h (37%, P less than 0.001) following the insulin infusion. In Study II (5 subjects) increments in plasma insulin concentration to 31 muU/ml resulted in no change in insulin binding at 3 h (P greater than 0.5) but resulted in a significant decrease at 5 h (25%, P less than 0.01). The plasma glucose concentration was maintained at basal levels in both infusion protocols. The decrease in insulin binding in both studies was due to a decrease in insulin receptor concentration. No significant change in receptor affinity was observed. In a control study (5 subjects) 5 h of saline infusion had no effect on insulin binding to monocytes. We conclude that in normal humans, increments in the plasma insulin concentration in the physiologic range downregulates the number of insulin receptors in a dose- and time-dependent manner.
为了直接研究生理性高胰岛素血症是否调节正常人的胰岛素受体,我们采用正常血糖胰岛素钳夹技术,研究了胰岛素输注对125I胰岛素与单核细胞结合的影响。在研究I(9名受试者)中,当稳态血浆胰岛素浓度升至约100 μU/ml时,胰岛素与单核细胞的结合在1小时时保持不变,但在胰岛素输注后3小时显著下降(20%,P<0.01),5小时时进一步下降(37%,P<0.001)。在研究II(5名受试者)中,血浆胰岛素浓度增加至31 μU/ml,3小时时胰岛素结合无变化(P>0.5),但5小时时显著下降(25%,P<0.01)。在两种输注方案中,血浆葡萄糖浓度均维持在基础水平。两项研究中胰岛素结合的下降是由于胰岛素受体浓度降低所致。未观察到受体亲和力的显著变化。在一项对照研究(5名受试者)中,输注生理盐水5小时对胰岛素与单核细胞的结合无影响。我们得出结论,在正常人体内,生理性范围内的血浆胰岛素浓度升高以剂量和时间依赖性方式下调胰岛素受体的数量。