Literature DB >> 3282947

Severe diabetes induced in subtotally depancreatized dogs by sustained hyperglycemia.

T Imamura1, M Koffler, J H Helderman, D Prince, R Thirlby, L Inman, R H Unger.   

Abstract

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.

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Year:  1988        PMID: 3282947     DOI: 10.2337/diab.37.5.600

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  21 in total

Review 1.  Canine diabetes mellitus: can old dogs teach us new tricks?

Authors:  B Catchpole; J M Ristic; L M Fleeman; L J Davison
Journal:  Diabetologia       Date:  2005-09-08       Impact factor: 10.122

2.  Preservation of insulin mRNA levels and insulin secretion in HIT cells by avoidance of chronic exposure to high glucose concentrations.

Authors:  R P Robertson; H J Zhang; K L Pyzdrowski; T F Walseth
Journal:  J Clin Invest       Date:  1992-08       Impact factor: 14.808

Review 3.  The beta cell lesion in type 2 diabetes: there has to be a primary functional abnormality.

Authors:  S E Kahn; S Zraika; K M Utzschneider; R L Hull
Journal:  Diabetologia       Date:  2009-03-27       Impact factor: 10.122

4.  Differentiation of glucose toxicity from beta cell exhaustion during the evolution of defective insulin gene expression in the pancreatic islet cell line, HIT-T15.

Authors:  A Moran; H J Zhang; L K Olson; J S Harmon; V Poitout; R P Robertson
Journal:  J Clin Invest       Date:  1997-02-01       Impact factor: 14.808

5.  Hyperglucagonemia precedes a decline in insulin secretion and causes hyperglycemia in chronically glucose-infused rats.

Authors:  Rachel A Jamison; Romana Stark; Jianying Dong; Shin Yonemitsu; Dongyan Zhang; Gerald I Shulman; Richard G Kibbey
Journal:  Am J Physiol Endocrinol Metab       Date:  2011-08-23       Impact factor: 4.310

6.  Intra-islet insulin permits glucose to directly suppress pancreatic A cell function.

Authors:  C J Greenbaum; P J Havel; G J Taborsky; L J Klaff
Journal:  J Clin Invest       Date:  1991-09       Impact factor: 14.808

7.  Chronic exposure of HIT cells to high glucose concentrations paradoxically decreases insulin gene transcription and alters binding of insulin gene regulatory protein.

Authors:  L K Olson; J B Redmon; H C Towle; R P Robertson
Journal:  J Clin Invest       Date:  1993-07       Impact factor: 14.808

8.  No glucotoxicity after 53 hours of 6.0 mmol/l hyperglycaemia in normal man.

Authors:  H Flax; D R Matthews; J C Levy; S W Coppack; R C Turner
Journal:  Diabetologia       Date:  1991-08       Impact factor: 10.122

9.  Prolonged exposure of human pancreatic islets to high glucose concentrations in vitro impairs the beta-cell function.

Authors:  D L Eizirik; G S Korbutt; C Hellerström
Journal:  J Clin Invest       Date:  1992-10       Impact factor: 14.808

10.  Beta cell mass and growth after syngeneic islet cell transplantation in normal and streptozocin diabetic C57BL/6 mice.

Authors:  E Montaña; S Bonner-Weir; G C Weir
Journal:  J Clin Invest       Date:  1993-03       Impact factor: 14.808

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