Laury M C, Takao F, Bailbe D, Penicaud L, Portha B, Picon L, Ktorza A
Laboratoire de Physiologie du Développement, CNRS URA 307, Université Paris VII, France.
Endocrinology. 1991 May;128(5):2526-33. doi: 10.1210/endo-128-5-2526.
The purpose of this study was to investigate the effects of a 48-h glucose (30% wt/vol) infusion in unrestrained catheterized healthy rats (HG) on subsequent in vivo and in vitro insulin response to glucose. High hyperglycemia (400-450 mg/dl) and resulting hyperinsulinemia (1.2 +/- 0.1 mU/ml vs. 0.15 +/- 0.03 mU/ml in controls) were maintained throughout the infusion period. Glucose-induced insulin secretion was examined in vivo 3 h after the end of infusion by performing either a glucose tolerance test or a hyperglycemic clamp (225 mg/dl for 60 min). In addition, in vivo insulin secretion was studied on day 1, 3, 5, and 7 after the end of glucose infusion by performing glucose tolerance tests. Insulin secretion was also investigated in vitro, using the isolated perfused pancreas technique, 3 h and 1 day post glucose infusion. During glucose tolerance tests and hyperglycemic clamps performed at 3 h, insulin secretion was much greater in HG rats than in controls, and remained increased until day 5. By contrast, when studied in vitro 3 h after the end of the infusion, glucose-induced insulin release from isolated perfused pancreases was impaired in HG rats as compared with controls, and the insulin response to arginine was dramatically increased. However, insulin secretion in vitro returned partially to normal after day 1. These data indicate that prolonged hyperglycemia has quite different effects on the subsequent insulin secretion in vivo or in vitro. It impairs, but reversibly, glucose-induced insulin secretion in vitro, whereas it increases it durably in vivo. This suggests that humoral and/or nervous interferences can counterbalance the possible perturbing effects of prolonged hyperglycemia on the normal B cell responsiveness to glucose.
本研究的目的是调查在无束缚且插有导管的健康大鼠(高糖组,HG)中进行48小时葡萄糖(30%重量/体积)输注对随后体内和体外胰岛素对葡萄糖反应的影响。在整个输注期间维持高血糖(400 - 450mg/dl)及由此导致的高胰岛素血症(1.2±0.1mU/ml,而对照组为0.15±0.03mU/ml)。输注结束3小时后,通过进行葡萄糖耐量试验或高血糖钳夹(225mg/dl,持续60分钟)在体内检测葡萄糖诱导的胰岛素分泌。此外,在葡萄糖输注结束后的第1、3、5和7天,通过进行葡萄糖耐量试验研究体内胰岛素分泌。在葡萄糖输注后3小时和1天,还使用离体灌注胰腺技术在体外研究胰岛素分泌。在3小时进行的葡萄糖耐量试验和高血糖钳夹期间,高糖组大鼠的胰岛素分泌比对照组大得多,并且一直增加到第5天。相比之下,在输注结束3小时后进行体外研究时,与对照组相比,高糖组大鼠离体灌注胰腺中葡萄糖诱导的胰岛素释放受损,并且对精氨酸的胰岛素反应显著增加。然而,体外胰岛素分泌在第1天后部分恢复正常。这些数据表明,长期高血糖对随后的体内或体外胰岛素分泌有截然不同的影响。它在体外损害但可逆地损害葡萄糖诱导的胰岛素分泌,而在体内则持久地增加胰岛素分泌。这表明体液和/或神经干扰可以抵消长期高血糖对正常B细胞对葡萄糖反应性可能产生的干扰作用。