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Diabetes, Vol 49, Issue 9 1492-1499, Copyright © 2000 by American Diabetes Association
Transgenic mice with increased hexosamine flux specifically targeted to beta-cells exhibit hyperinsulinemia and peripheral insulin resistance
J Tang, JL Neidigh, RC Cooksey and DA McClain
Department of Internal Medicine, University of Utah, Salt Lake City 84132, USA.
Hexosamines have been shown to mediate effects of hyperglycemia and
so-called "glucose toxicity" in insulin-sensitive tissues. To determine the
effects of hexosamines on insulin synthesis and secretion, transgenic mice
were created to overexpress the rate-limiting enzyme for hexosamine
synthesis, glutamine:fructose-6-phosphate amidotransferase (GFA),
specifically in beta-cells. GFA activity in islets of heterozygous
transgenic mice was elevated 76% compared with littermate controls. The
increased GFA activity led to 1.4- and 2.1-fold increased pancreatic
insulin content in 2- and 10-month-old transgenic mice, respectively (P
< 0.005). Fasting insulin levels were 1.6-fold higher than in littermate
controls (P < 0.05). Hyperinsulinemia was evident despite a 28%
reduction in insulin mRNA levels. The fasting glucose levels in the
transgenic mice equaled that of controls aged 2-4 months but exceeded that
of the controls aged 6-10 months (means +/- SE 6.9 +/- 0.2 vs. 5.9 +/- 0.2
mmol/l, P < 0.001). By 8 months, the males were overweight and mildly
diabetic (fasting glucose 8.8 +/- 0.5 mmol/l) despite persistent
hyperinsulinemia. Insulin resistance was confirmed in both males and
females using the euglycemic-hyperinsulinemic clamp technique; glucose
disposal rates decreased by 48% in transgenic mice (P < 0.01).
Triglyceride levels did not differ, and free fatty acid levels were lower
in the transgenic animals. ATP levels were unchanged in the transgenic
islets. We conclude that hexosamine biosynthesis is involved in the
regulation of insulin content in beta-cells by glucose. Increased
hexosamine flux in the beta-cell results in hyperinsulinemia, insulin
resistance, and (in males) mild type 2 diabetes.

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Copyright © 2000 by the American Diabetes Association.
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