Nesher R, Tuch B, Hage C, Levy J, Cerasi E
Diabetologia. 1984 Feb;26(2):142-5. doi: 10.1007/BF00281122.
Brief stimulation of the pancreas with arginine causes a refractory state which reduces the insulin response to subsequent stimulations (time-dependent inhibition). In control subjects, a pair of arginine injections (75 mg/kg) at a 30-min interval resulted in 20% reduction of peak and integrated insulin responses to the second injection. In Type 2 (non-insulin-dependent) diabetic patients and in obese subjects, the inhibitory effect of repeated arginine stimuli was abolished. Healthy subjects were made acutely hyperglycaemic (9.3 +/- 0.3 mmol/l) by the glucose clamp technique. This induced a three- to fivefold greater insulin response to arginine. Compared to the response of diabetic subjects with similar hyperglycaemia, the control subjects secreted four to nine times more insulin. When the arginine stimulation was repeated 30 min later, no inhibition was observed, the second insulin response being instead augmented 1.5- to 1.8-fold. We conclude that (1) the insulin response to arginine is markedly reduced in Type 2 diabetes; (2) arginine-induced time-dependent inhibition of insulin release is abolished in patients with minimal to moderate hyperglycaemia; (3) this is probably due to the acute synergistic action of glucose and arginine on the B cell; (4) time-dependent inhibition of insulin release may be a protective mechanism against insulin oversecretion following repetitive stimulation of the pancreas; its abolition in hyperglycaemic states may be a compensatory mechanism, allowing substantial increases in insulin output.
用精氨酸对胰腺进行短暂刺激会导致一种不应期状态,从而降低胰岛素对后续刺激的反应(时间依赖性抑制)。在对照受试者中,以30分钟的间隔注射一对精氨酸(75毫克/千克)会使对第二次注射的胰岛素峰值和积分反应降低20%。在2型(非胰岛素依赖型)糖尿病患者和肥胖受试者中,重复精氨酸刺激的抑制作用消失。通过葡萄糖钳夹技术使健康受试者急性高血糖(9.3±0.3毫摩尔/升)。这导致对精氨酸的胰岛素反应增加三到五倍。与具有相似高血糖的糖尿病受试者的反应相比,对照受试者分泌的胰岛素多四到九倍。当30分钟后重复精氨酸刺激时,未观察到抑制作用,第二次胰岛素反应反而增加了1.5到1.8倍。我们得出结论:(1)2型糖尿病患者对精氨酸的胰岛素反应明显降低;(2)在轻度至中度高血糖患者中,精氨酸诱导的胰岛素释放时间依赖性抑制作用消失;(3)这可能是由于葡萄糖和精氨酸对B细胞的急性协同作用;(4)胰岛素释放的时间依赖性抑制可能是一种保护机制,可防止胰腺重复刺激后胰岛素分泌过多;在高血糖状态下其消失可能是一种补偿机制,可使胰岛素输出大幅增加。