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Lookup NU author(s): Dr Ziad Al-Oanzi,
Dr Susan Tudhope,
Dr Gillian Patman,
Dr Catherine ArdenORCiD,
Professor Helen ReevesORCiD,
Professor Loranne Agius
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Wiley-Blackwell, 2017.
For re-use rights please refer to the publisher's terms and conditions.
Aim: Small molecule activators of glucokinase (GKAs) have been extensively explored as potential anti-hyperglycaemic drugs for type 2 diabetes (T2D). Several GKAs were remarkably effective at lowering blood glucose during early therapy but then lost their glycaemic efficacy chronically during clinical trials. We used rat hepatocytes to test the hypothesis that GKAs raise hepatocyte glucose 6-phosphate, (G6P, the glucokinase product) and down-stream metabolites with consequent repression of the liver glucokinase gene (Gck). We compared a GKA with metformin, the most widely prescribed drug for T2D. Results: Treatment of hepatocytes with 25mM glucose raised cell G6P concomitantly with Gck repression and induction of G6pc (glucose 6-phosphatase) and Pklr (pyruvate kinase). A GKA mimicked high glucose by raising G6P and fructose-2,6-bisphosphate, a regulatory metabolite, causing a left-shift in glucose responsiveness on gene regulation. Fructose like the GKA repressed Gck but modestly induced G6pc. 2-Deoxyglucose, which is phosphorylated by glucokinase, but not further metabolised caused Gck repression but not G6pc induction, implicating the glucokinase product in Gck repression. Metformin counteracted the effect of high glucose on the elevated G6P and fructose 2,6-bisphosphate and on Gck repression, recruitment of Mlx-ChREBP to the G6pc and Pklr promoters and induction of these genes. Conclusions: 1. Elevation in hepatocyte G6P and downstream metabolites with consequent liver Gck repression is a potential contributing mechanism to the loss of GKA efficacy during chronic therapy. 2. Cell metformin loads within the therapeutic range attenuate the effect of high glucose on G6P and on glucose-regulated gene expression.
Author(s): Al-Oanzi ZH, Fountana S, Moonira T, Tudhope SJ, Petrie JL, Alshawi A, Patman G, Arden C, Reeves HL, Agius L
Publication type: Article
Publication status: Published
Journal: Diabetes, Obesity and Metabolism
Print publication date: 01/08/2017
Online publication date: 16/02/2017
Acceptance date: 11/02/2017
Date deposited: 13/02/2017
ISSN (print): 1462-8902
ISSN (electronic): 1463-1326
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