Glucokinase gene locus transgenic mice are resistant to the development of obesity-induced type 2 diabetes

被引:51
作者
Shiota, M
Postic, C
Fujimoto, Y
Jetton, TL
Dixon, K
Pan, DH
Grimsby, J
Grippo, JF
Magnuson, MA
Cherrington, AD
机构
[1] Vanderbilt Univ, Sch Med, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2] Hoffmann La Roche Inc, Dept Metab Dis, Nutley, NJ 07110 USA
关键词
D O I
10.2337/diabetes.50.3.622
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transgenic mice that overexpress the entire glucokinase (GK) gene locus have been previously shown to be mildly hypoglycemic and to have improved tolerance to glucose. To determine whether increased GK might also prevent or diminish diabetes in diet-induced obese animals, we examined the effect of feeding these mice a high-fat high-simple carbohydrate low-fiber diet (HF diet) for 30 weeks. In response to this diet, both normal and transgenic mice became obese and had similar BMIs (5.3 +/- 0.1 and 5.0 +/- 0.1 kg/m(2) in transgenic and nontransgenic mice, respectively). The blood glucose concentration of the control mice increased linearly with time and reached 17.0 +/- 1.3 mmol/l at the 30th week. In contrast, the blood glucose of GK transgenic mice rose to only 9.7 +/- 1.2 mmol/l at the 15th week, after which it returned to 7.6 +/- 1.0 mmol/l by the 30th week. The plasma insulin concentration was also lower in the GK transgenic animals (232 +/- 79 pmol/l) than in the controls (595 +/- 77 pmol/l), but there was no difference in plasma glucagon concentrations. Together, these data indicate that increased GK levels dramatically lessen the development of both hyperglycemia and hyperinsulinemia associated with the feeding of an HF diet.
引用
收藏
页码:622 / 629
页数:8
相关论文
共 79 条
[1]   INTRACELLULAR BINDING OF GLUCOKINASE IN HEPATOCYTES AND TRANSLOCATION BY GLUCOSE, FRUCTOSE AND INSULIN [J].
AGIUS, L ;
PEAK, M .
BIOCHEMICAL JOURNAL, 1993, 296 :785-796
[2]  
ANDRIKOPOULOS S, 1995, DIABETOLOGIA, V38, P1383
[3]   Regulation of rat liver glucose-6-phosphatase gene expression in different nutritional and hormonal states - Gene structure and 5'-flanking sequence [J].
Argaud, D ;
Zhang, Q ;
Pan, WS ;
Maitra, S ;
Pilkis, SJ ;
Lange, AJ .
DIABETES, 1996, 45 (11) :1563-1571
[4]   Stimulation of glucose-6-phosphatase gene expression by glucose and fructose-2,6-bisphosphate [J].
Argaud, D ;
Kirby, TL ;
Newgard, CB ;
Lange, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (19) :12854-12861
[5]   ANIMAL-MODEL FOR MATURITY-ONSET DIABETES OF THE YOUNG GENERATED BY DISRUPTION OF THE MOUSE GLUCOKINASE GENE [J].
BALI, D ;
SVETLANOV, A ;
LEE, HW ;
FUSCODEMANE, D ;
LEISER, M ;
LI, BJ ;
BARZILAI, N ;
SURANA, M ;
HOU, H ;
FLEISCHER, N ;
DEPINHO, R ;
ROSSETTI, L ;
EFRAT, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21464-21467
[6]   Glucosamine-induced inhibition of liver glucokinase impairs the ability of hyperglycemia to suppress endogenous glucose production [J].
Barzilai, N ;
Hawkins, M ;
Angelov, I ;
Hu, MZ ;
Rossetti, L .
DIABETES, 1996, 45 (10) :1329-1335
[7]  
BARZILAI N, 1993, J BIOL CHEM, V268, P25019
[8]  
BELFIORE F, 1987, INT J OBESITY, V11, P631
[9]   THE EFFECT OF CHRONIC SULFONYLUREA THERAPY ON HEPATIC GLUCOSE-PRODUCTION IN NON-INSULIN-DEPENDENT DIABETES [J].
BEST, JD ;
JUDZEWITSCH, RG ;
PFEIFER, MA ;
BEARD, JC ;
HALTER, JB ;
PORTE, D .
DIABETES, 1982, 31 (04) :333-338
[10]   PARTIAL PANCREATECTOMY IN THE RAT AND SUBSEQUENT DEFECT IN GLUCOSE-INDUCED INSULIN RELEASE [J].
BONNERWEIR, S ;
TRENT, DF ;
WEIR, GC .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (06) :1544-1553