Rossetti L, Shulman G I, Zawalich W, DeFronzo R A
Yale University School of Medicine, New Haven, Connecticut 06510.
J Clin Invest. 1987 Oct;80(4):1037-44. doi: 10.1172/JCI113157.
We have examined the effect of chronic (4 wk) hyperglycemia on insulin secretion in vivo in an awake, unstressed rat model. Three groups of animals were examined: control, partial (90%) pancreatectomy, and partial pancreatectomy plus phlorizin, in order to normalize plasma glucose levels. Insulin secretion in response to arginine (2 mM), hyperglycemia (+100 mg/dl), and arginine plus hyperglycemia was evaluated. In diabetic compared with control animals three specific alterations were observed: (a) a deficient insulin response, in both first and second phases, to hyperglycemia; (b) an augmented insulin response to the potentiating effect of arginine under basal glycemic conditions; and (c) an inability of hyperglycemia to augment the potentiating effect of arginine above that observed under basal glycemic conditions. Normalization of the plasma glucose profile by phlorizin treatment in diabetic rats completely corrected all three beta cell abnormalities. These results indicate that chronic hyperglycemia can lead to a defect in in vivo insulin secretion which is reversible when normoglycemia is restored.
我们在清醒、无应激的大鼠模型中研究了慢性(4周)高血糖对体内胰岛素分泌的影响。研究了三组动物:对照组、部分(90%)胰腺切除术组以及部分胰腺切除术加根皮苷组,后者用于使血糖水平正常化。评估了对精氨酸(2 mM)、高血糖(+100 mg/dl)以及精氨酸加高血糖的胰岛素分泌情况。与对照动物相比,糖尿病动物出现了三种特定改变:(a)在高血糖的第一和第二阶段,胰岛素反应不足;(b)在基础血糖条件下,对精氨酸增强作用的胰岛素反应增强;(c)高血糖无法增强精氨酸的增强作用,使其超过基础血糖条件下观察到的水平。用根皮苷治疗糖尿病大鼠使血糖水平正常化,完全纠正了所有这三种β细胞异常。这些结果表明,慢性高血糖可导致体内胰岛素分泌缺陷,当恢复正常血糖时该缺陷是可逆的。