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Am J Physiol Endocrinol Metab 287: E414-E423, 2004. First published May 11, 2004; doi:10.1152/ajpendo.00575.2003
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Defect in glucokinase translocation in Zucker diabetic fatty rats

Yuka Fujimoto, E. Patrick Donahue, and Masakazu Shiota

Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232

Submitted 17 December 2003 ; accepted in final form 29 April 2004

Hepatic glucose fluxes and intracellular movement of glucokinase (GK) in response to increased plasma glucose and insulin were examined in 10-wk-old, 6-h-fasted, conscious Zucker diabetic fatty (ZDF) rats and lean littermates. Under basal conditions, plasma glucose (mmol/l) and glucose turnover rate (GTR; µmol·kg–1·min–1) were slightly higher in ZDF (8.4 ± 0.3 and 53 ± 7, respectively) than in lean rats (6.2 ± 0.2 and 45 ± 4, respectively), whereas plasma insulin (pmol/l) was higher in ZDF (1,800 ± 350) than in lean rats (150 ± 14). The ratio of hepatic uridine 5'-diphosphate-glucose 3H specific activity to plasma glucose 3H specific activity ([3H]UDP-G/[3H]G; %), total hepatic glucose output (µmol·kg–1·min–1), and hepatic glucose cycling (µmol·kg–1·min–1) were higher in ZDF (35 ± 5, 87 ± 16, and 33 ± 10, respectively) compared with lean rats (18 ± 3, 56 ± 6, and 11 ± 2, respectively). [3H]glucose incorporation into glycogen (µmol glucose/g liver) was similar in lean (1.0 ± 0.7) and ZDF (1.6 ± 0.8) rats. GK was predominantly located in the nucleus in both rats. With elevated plasma glucose and insulin, GTR (µmol·kg–1·min–1), [3H]UDP-G/[3H]G (%), and [3H]glucose incorporation into glycogen (µmol glucose/g liver) were markedly higher in lean (191 ± 22, 62 ± 3, and 5.0 ± 1.4, respectively) but similar in ZDF rats (100 ± 6, 37 ± 3, and 1.4 ± 0.4, respectively) compared with basal conditions. GK translocation from the nucleus to the cytoplasm occurred in lean but not in ZDF rats. The unresponsiveness of hepatic glucose flux to the rise in plasma glucose and insulin seen in prediabetic ZDF rats was associated with impaired GK translocation.

liver; glucose flux; insulin; hyperglycemia



Address for reprint requests and other correspondence: M. Shiota, Dept. of Molecular Physiology and Biophysics, Vanderbilt Univ. School of Medicine, 702 Light Hall, Nashville, TN 37232–0615 (E-mail: masakazu.shiota{at}vanderbilt.edu).




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