Kerner W, Beischer W, Maier V, Pfeiffer E F
Horm Metab Res Suppl. 1979(8):71-80.
The influence of different control modes for insulin infusion with an artificial beta cell was examined in 41 insulin-dependent diabetics. In 21 Patients, oral glucose tolerance tests were performed with control modes characterized either by low dynamic and high static gain (type I, 10 patients) or high dynamic and low static gain (type III, 11 patients). The change from type I to type III control mode effected an increase of initial insulin infusion rates (91 +/- 59 to 313 +/- 81 mU/min 10-20 min after glucose ingestion) and a decrease of infusion rates during the following phase of the 3-hour observation period (28.2 +/- 4.2 to 18.1 +/- 2.8 U) in patients whose blood glucose curves were completely normalized. Suppression of plasma glucagon levels, observed in 5 healthy control subjects, was not fully restored to normal in these patients. In another 20 insulin-dependent diabetics, daily insulin requirements form the artificial beta cell were determined by employing two control modes (types II and III) comparable in static control but different in dynamic control. Gain of dynamic control, especially in the range of falling glucose levels, was higher in type III control mode (15 patients) than in type II mode (5 patients). These insulin requirements were compared to the insulin doses necessary for subcutaneous treatment. While intravenous insulin requirements were much higher when type II control mode was employed (78.2 +/- 10.2%), during application of type III mode, intravenous insulin requirements were only 10.8 +/- 5.5% higher than subcutaneous doses. We conclude from these data that early increases in insulin infusion rates followed by a rapid decrease seem to reduce insulin requirements after glucose ingestion. A high-gain dynamic control is the basis for this insulin infusion profile.
在41例胰岛素依赖型糖尿病患者中,研究了人工β细胞输注胰岛素的不同控制模式的影响。对21例患者进行了口服葡萄糖耐量试验,其控制模式的特点为低动态增益和高静态增益(I型,10例患者)或高动态增益和低静态增益(III型,11例患者)。对于血糖曲线完全正常化的患者,从I型控制模式转变为III型控制模式,会使初始胰岛素输注速率增加(摄入葡萄糖后10 - 20分钟,从91±59增加至313±81 mU/分钟),并使3小时观察期后续阶段的输注速率降低(从28.2±4.2降至18.1±2.8 U)。在5名健康对照受试者中观察到的血浆胰高血糖素水平抑制,在这些患者中未完全恢复正常。在另外20例胰岛素依赖型糖尿病患者中,通过采用两种静态控制相当但动态控制不同的控制模式(II型和III型),确定了人工β细胞的每日胰岛素需求量。III型控制模式(15例患者)在动态控制增益方面,尤其是在血糖水平下降范围内,高于II型模式(5例患者)。将这些胰岛素需求量与皮下治疗所需的胰岛素剂量进行了比较。当采用II型控制模式时,静脉胰岛素需求量要高得多(78.2±10.2%),而在应用III型模式时,静脉胰岛素需求量仅比皮下剂量高10.8±5.5%。从这些数据中我们得出结论,摄入葡萄糖后胰岛素输注速率早期增加随后迅速降低似乎会减少胰岛素需求量。高增益动态控制是这种胰岛素输注模式的基础。