GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com

TableEdit

Jump to: navigation, search

PMID:17028192

You don't have sufficient rights on this wiki to edit tables. Perhaps you need to log in. Changes you make in the Table editor will not be saved back to the wiki

See Help for Help on this wiki. See the documentation for how to use the table editor

Citation

Futamura, M, Hosaka, H, Kadotani, A, Shimazaki, H, Sasaki, K, Ohyama, S, Nishimura, T, Eiki, J and Nagata, Y (2006) An allosteric activator of glucokinase impairs the interaction of glucokinase and glucokinase regulatory protein and regulates glucose metabolism. J. Biol. Chem. 281:37668-74

Abstract

Glucokinase (GK) plays a key role in the control of blood glucose homeostasis. We identified a small molecule GK activator, compound A, that increased the glucose affinity and maximal velocity (V(max)) of GK. Compound A augmented insulin secretion from isolated rat islets and enhanced glucose utilization in primary cultured rat hepatocytes. In rat oral glucose tolerance tests, orally administrated compound A lowered plasma glucose elevation with a concomitant increase in plasma insulin and hepatic glycogen. In liver, GK activity is acutely controlled by its association to the glucokinase regulatory protein (GKRP). In order to decipher the molecular aspects of how GK activator affects the shuttling of GK between nucleus and cytoplasm, the effect of compound A on GK-GKRP interaction was further investigated. Compound A increased the level of cytoplasmic GK in both isolated rat primary hepatocytes and the liver tissues from rats. Experiments in a cell-free system revealed that compound A interacted with glucose-bound free GK, thereby impairing the association of GK and GKRP. On the other hand, compound A did not bind to glucose-unbound GK or GKRP-associated GK. Furthermore, we found that glucose-dependent GK-GKRP interaction also required ATP. Given the combined prominent role of GK on insulin secretion and hepatic glucose metabolism where the GK-GKRP mechanism is involved, activation of GK has a new therapeutic potential in the treatment of type 2 diabetes.

Links

PubMed Online version:10.1074/jbc.M605186200

Keywords

Active Transport, Cell Nucleus/drug effects; Adaptor Proteins, Signal Transducing/genetics; Adaptor Proteins, Signal Transducing/metabolism; Adenosine Triphosphate/metabolism; Adenosine Triphosphate/pharmacology; Allosteric Regulation; Animals; Benzamides/chemistry; Benzamides/pharmacology; Carrier Proteins/genetics; Carrier Proteins/metabolism; Cell-Free System; Cells, Cultured; Enzyme Activation/drug effects; Glucokinase/genetics; Glucokinase/metabolism; Glucose/metabolism; Glucose/pharmacology; Hepatocytes/drug effects; Hepatocytes/metabolism; Humans; Insulin/secretion; Islets of Langerhans/drug effects; Islets of Langerhans/secretion; Male; Rats; Rats, Wistar; Recombinant Proteins/genetics; Recombinant Proteins/metabolism

public



Cancel