Sako Y, Grill V E
Department of Endocrinology, Karolinska Hospital, Stockholm, Sweden.
Diabetes. 1990 Dec;39(12):1580-3. doi: 10.2337/diab.39.12.1580.
Nondiabetic rats were infused with glucose for 48 h to maintain moderate or marked hyperglycemia (mean blood glucose 13.2 +/- 0.7 or 22.8 +/- 0.3 mM, respectively). The two levels of hyperglycemia increased plasma insulin levels severalfold but decreased the insulin response to 27 mM glucose by 19 and 95%, respectively, versus saline infusion. Diazoxide (5 mg.kg-1.h-1), when continuously infused during the hyperglycemia protocols, completely inhibited the glucose-induced rise in plasma insulin levels. Diazoxide transformed beta-cell insensitivity to stimulation: glucose-induced insulin release was thus increased 318% after moderate hyperglycemia and 707% after marked hyperglycemia. These stimulatory effects of diazoxide were reversed by exogenous insulin infusion (8 or 2 U/24 h) in a dose-dependent manner. It is concluded that excessive beta-cell stimulation rather than glucotoxicity underlies hyperglycemia-induced beta-cell insensitivity. Effects of hyperinsulinemia can form part of the mechanisms whereby excessive stimulation affects beta-cell secretion.
将非糖尿病大鼠输注葡萄糖48小时以维持中度或显著高血糖(平均血糖分别为13.2±0.7或22.8±0.3 mM)。与输注生理盐水相比,这两种高血糖水平使血浆胰岛素水平升高了几倍,但使胰岛素对27 mM葡萄糖的反应分别降低了19%和95%。在高血糖方案期间持续输注二氮嗪(5 mg·kg-1·h-1),可完全抑制葡萄糖诱导的血浆胰岛素水平升高。二氮嗪改变了β细胞对刺激的不敏感性:因此,中度高血糖后葡萄糖诱导的胰岛素释放增加了318%,显著高血糖后增加了707%。外源性胰岛素输注(8或2 U/24 h)以剂量依赖的方式逆转了二氮嗪的这些刺激作用。得出的结论是,高血糖诱导的β细胞不敏感性的基础是β细胞过度刺激而非糖毒性。高胰岛素血症的影响可能是过度刺激影响β细胞分泌的机制的一部分。