Allosteric activators of glucokinase: Potential role in diabetes therapy

被引:440
作者
Grimsby, J
Sarabu, R
Corbett, WL
Haynes, NE
Bizzarro, FT
Coffey, JW
Guertin, KR
Hilliard, DW
Kester, RF
Mahaney, PE
Marcus, L
Qi, LD
Spence, CL
Tengi, J
Magnuson, MA
Chu, CA
Dvorozniak, MT
Matschinsky, FM
Grippo, JF
机构
[1] Hoffmann La Roche Inc, Dept Metab Dis, Nutley, NJ 07110 USA
[2] Vanderbilt Univ, Dept Physiol & Mol Biophys, Nashville, TN 37232 USA
[3] Univ Penn, Sch Med, Dept Biochem, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Ctr Diabet, Philadelphia, PA 19104 USA
关键词
D O I
10.1126/science.1084073
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Glucokinase (GK) plays a key role in whole-body glucose homeostasis by catalyzing the phosphorylation of glucose in cells that express this enzyme, such as pancreatic beta cells and hepatocytes. We describe a class of antidiabetic agents that act as nonessential, mixed-type GK activators (GKAs) that increase the glucose affinity and maximum velocity (V-max) of GK. GKAs augment both hepatic glucose metabolism and glucose-induced insulin secretion from isolated rodent pancreatic islets, consistent with the expression and function of GK in both cell types. In several rodent models of type 2 diabetes mellitus, GKAs lowered blood glucose levels, improved the results of glucose tolerance tests, and increased hepatic glucose uptake. These findings may lead to the development of new drug therapies for diabetes.
引用
收藏
页码:370 / 373
页数:4
相关论文
共 21 条
[1]
BELL GI, 2002, ENCY MOL MED, P1437
[2]
The second activating glucokinase mutation (A456V) - Implications for glucose homeostasis and diabetes therapy [J].
Christesen, HBT ;
Jacobsen, BB ;
Odili, S ;
Buettger, C ;
Cuesta-Munoz, A ;
Hansen, T ;
Brusgaard, K ;
Massa, O ;
Magnuson, MA ;
Shiota, C ;
Matschinsky, FM ;
Barbetti, F .
DIABETES, 2002, 51 (04) :1240-1246
[3]
Clement K, 1996, DIABETOLOGIA, V39, P82
[4]
Mutants of glucokinase cause hypoglycaemia- and hyperglycaemia syndromes and their analysis illuminates fundamental quantitative concepts of glucose homeostasis [J].
Davis, EA ;
Cuesta-Muñoz, A ;
Raoul, M ;
Buettger, C ;
Sweet, I ;
Moates, M ;
Magnuson, MA ;
Matschinsky, FM .
DIABETOLOGIA, 1999, 42 (10) :1175-1186
[5]
THE TRIUMVIRATE - BETA-CELL, MUSCLE, LIVER - A COLLUSION RESPONSIBLE FOR NIDDM [J].
DEFRONZO, RA .
DIABETES, 1988, 37 (06) :667-687
[6]
Phenotypic correction of diabetic mice by adenovirus-mediated glucokinase expression [J].
Desai, UJ ;
Slosberg, ED ;
Boettcher, BR ;
Caplan, SL ;
Fanelli, B ;
Stephan, Z ;
Gunther, VJ ;
Kaleko, M ;
Connelly, S .
DIABETES, 2001, 50 (10) :2287-2295
[7]
Correction of diabetic alterations by glucokinase [J].
Ferre, T ;
Pujol, A ;
Riu, E ;
Bosch, F ;
Valera, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7225-7230
[8]
GLUCOKINASE MUTATIONS ASSOCIATED WITH NON-INSULIN-DEPENDENT (TYPE-2) DIABETES-MELLITUS HAVE DECREASED ENZYMATIC-ACTIVITY - IMPLICATIONS FOR STRUCTURE-FUNCTION-RELATIONSHIPS [J].
GIDHJAIN, M ;
TAKEDA, J ;
XU, LZ ;
LANGE, AJ ;
VIONNET, N ;
STOFFEL, M ;
FROGUEL, P ;
VELHO, G ;
SUN, F ;
COHEN, D ;
PATEL, P ;
LO, YMD ;
HATTERSLEY, AT ;
LUTHMAN, H ;
WEDELL, A ;
STCHARLES, R ;
HARRISON, RW ;
WEBER, IT ;
BELL, GI ;
PILKIS, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1932-1936
[9]
Familial hyperinsulinism caused by an activating glucokinase mutation [J].
Glaser, B ;
Kesavan, P ;
Heyman, M ;
Davis, E ;
Cuesta, A ;
Buchs, A ;
Stanley, CA ;
Thornton, PS ;
Permutt, MA ;
Matschinsky, FM ;
Herold, KC .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (04) :226-230
[10]
GRIMSBY J, UNPUB