Imamura T, Koffler M, Helderman J H, Prince D, Thirlby R, Inman L, Unger R H
Center for Diabetes Research, University of Texas Health Science Center, Dallas 75235.
Diabetes. 1988 May;37(5):600-9. doi: 10.2337/diab.37.5.600.
Chronic clamping of plasma glucose levels at greater than or equal to 250 mg/dl in four partially depancreatized but previously nondiabetic dogs was followed within 2 wk by persistent hyperglycemia and glycosuria of less than or equal to 500 g/day, ketonuria, and weight loss. Three of the four dogs required daily insulin injections to control these catabolic manifestations. There was no evidence of spontaneous improvement of the severe diabetic state during the 39-69 days of observation after discontinuation of intravenous glucose infusion. Impairment of intravenous glucose tolerance, loss of the insulin response to glucose and arginine, fasting hyperglucagonemia, exaggerated glucagon responsiveness to arginine, and a significant reduction in sensitivity to insulin were characteristic of all diabetic dogs. Morphometric analysis of the endocrine pancreas revealed a profound reduction in the number and size of identifiable islets of the hyperglycemic dogs compared with islets from their own pancreases resected months earlier and with those from pancreatic remnants of eight subtotally depancreatized control dogs that had not been subjected to chronic hyperglycemic clamping. The reduction in number and size of islets of the hyperglycemic dogs was largely the consequence of depletion of insulin-containing cells and was similar to that of dogs with long-standing alloxan-induced diabetes. In the eight control dogs, clinical evidence of diabetes did not develop during a follow-up period of 193-296 days. In this group, there was no evidence of diminution of intravenous glucose tolerance, of the insulin response to glucose or arginine, or of insulin sensitivity as determined by an acute hyperinsulinemic hyperglycemic clamp. The number and size of islets and number of beta-cells in pancreatic remnants from these dogs did not differ morphometrically from those of the pancreatic segment that had been resected. We conclude that in subtotally depancreatized but nondiabetic dogs, maintenance of constant hyperglycemia of greater than or equal to 250 mg/dl by means of intravenous glucose infusion causes a severe, persistent, and often insulin-requiring diabetic state that does not occur in the absence of the hyperglycemia.
对四只部分胰腺切除但先前无糖尿病的狗持续钳夹血浆葡萄糖水平,使其维持在大于或等于250mg/dl,两周内出现持续高血糖和每日尿糖量小于或等于500g、酮尿和体重减轻。四只狗中有三只需要每日注射胰岛素以控制这些分解代谢表现。在停止静脉输注葡萄糖后的39 - 69天观察期内,未发现严重糖尿病状态有自发改善的迹象。静脉葡萄糖耐量受损、对葡萄糖和精氨酸的胰岛素反应丧失、空腹高胰高血糖素血症、胰高血糖素对精氨酸的反应性增强以及对胰岛素敏感性显著降低是所有糖尿病狗的特征。对内分泌胰腺的形态计量学分析显示,与数月前切除的自身胰腺中的胰岛以及八只接受次全胰腺切除但未进行慢性高血糖钳夹的对照狗的胰腺残余中的胰岛相比,高血糖狗中可识别胰岛的数量和大小显著减少。高血糖狗胰岛数量和大小的减少主要是含胰岛素细胞耗竭的结果,与长期用四氧嘧啶诱导糖尿病的狗相似。在八只对照狗中,在193 - 296天的随访期内未出现糖尿病的临床证据。在该组中,未发现静脉葡萄糖耐量、对葡萄糖或精氨酸的胰岛素反应或通过急性高胰岛素血症 - 高血糖钳夹测定的胰岛素敏感性有降低的迹象。这些狗胰腺残余中的胰岛数量、大小和β细胞数量在形态计量学上与切除的胰腺节段无差异。我们得出结论,在次全胰腺切除但无糖尿病的狗中,通过静脉输注葡萄糖维持大于或等于250mg/dl的持续高血糖会导致严重、持续且通常需要胰岛素治疗的糖尿病状态,若无高血糖则不会发生这种情况。