Ferrannini E, Pilo A
J Clin Invest. 1979 Jul;64(1):243-54. doi: 10.1172/JCI109445.
Plasma insulin concentrations after pulse intravenous injection of glucose show an early rise, which declines towards the prestimulation level smoothly. This pattern is the effect of both continuing secretion and hormone disappearance from the plasma. To reconstruct the time-course of the acutal secretory response, we measured insulin disappearance from the plasma of 17 healthy volunteers by means of a bolus intravenous injection of 125I-insulin, and then performed an intravenous glucose tolerance test with frequent blood sampling. The data were analyzed by deconvolution, which made it possible to compute the glucose-induced posthepatic insulin delivery rate minute by minute. Under basal conditions, 2.64 +/- 0.28 (mean +/-SEM) mU/min.m2 reaches the systemic circulation. In the 90 min that follow acute glucose stimulation, 0.86 +/- 0.11 U/m2, a 270% increment over the basal production rate, is made available to the periphery. A wide individual variability was found to exist in both the basal and the glucose-stimulated delivery. They were strongly (P less than 0.001) related to each other in a direct fashion. A first spike of insulin release (107 +/- 12 mU/min) occurred in all the subjects at 2.2 +/- 0.2 min followed, in 16 subjects, by a second spike (38 +/- 6 mU/min), at 11.3 +/- 0.9 min. Two-thirds of the total postglucose insulin output were associated with the initial, oscillatory phase (from 0 to 25 min, on average), and one-third with the "tail" phase (from 25 to 90 min), during which the average delivery rate was 5.0 +/- 0.9 mU/min.m2. The delivery curves were closely (mean squared deviation of 4.5 +/- 0.5 mU/min) reproduced by computer stimulation upon assuming that insulin secretion is a function of both glucose concentration and glucose rate of change. Both the first and the second spike of insulin delivery, but not the total insulin output during the test, showed a significant, positive correlation with the plasma glucose disappearance rate computed between 10 and 60 min. Furthermore, with a time shift of approximately equal to 15 min, a significant relationship between the phases of insulin secretion and the glucose decay rates, computed over corresponding time intervals, was evident throughout the test.
脉冲静脉注射葡萄糖后血浆胰岛素浓度早期升高,随后平稳下降至刺激前水平。这种模式是持续分泌和激素从血浆中消失共同作用的结果。为了重建实际分泌反应的时间进程,我们通过大剂量静脉注射125I - 胰岛素来测量17名健康志愿者血浆中胰岛素的消失情况,然后进行频繁采血的静脉葡萄糖耐量试验。通过去卷积分析数据,从而能够逐分钟计算葡萄糖诱导的肝后胰岛素输送率。在基础状态下,2.64±0.28(均值±标准误)mU/分钟·m²进入体循环。在急性葡萄糖刺激后的90分钟内,0.86±0.11 U/m²进入外周,较基础产生率增加了270%。发现基础和葡萄糖刺激后的输送量个体差异很大。两者呈强正相关(P<0.001)。所有受试者在2.2±0.2分钟时出现第一个胰岛素释放峰值(107±12 mU/分钟),16名受试者在11.3±0.9分钟时出现第二个峰值(38±6 mU/分钟)。葡萄糖刺激后胰岛素总输出量的三分之二与初始振荡期(平均从0到25分钟)相关,三分之一与“尾”期(从25到90分钟)相关,在此期间平均输送率为5.0±0.9 mU/分钟·m²。假设胰岛素分泌是葡萄糖浓度和葡萄糖变化率的函数,通过计算机模拟可紧密重现输送曲线(均方偏差为4.5±0.5 mU/分钟)。胰岛素输送的第一个和第二个峰值,而非试验期间的胰岛素总输出量,与10至60分钟计算的血浆葡萄糖消失率呈显著正相关。此外,大约有15分钟的时间偏移,在整个试验中,胰岛素分泌阶段与相应时间间隔计算的葡萄糖衰减率之间存在显著关系。