PSN-GK1

Kinase experiment:

Glucokinase activity is measured in a coupled reaction with glucose-6-phosphate dehydrogenase (G6PDH) by monitoring NADPH production at A340 in a plate reader after 15 min incubation at 24°C, in a final volume of 100 μL containing 25 mM HEPES pH 7.1, 25 mM KCl, 5 mM glucose, 1 mM ATP, 2 mM MgCl2, 1 mM DL-dithiothreitol, 1 mM NADP, 2.5 U/mL G6PDH, 0.4 μg GST-glucokinase. Ten dilutions of PSN-GK1 from 0.004 to 100 μM are tested, calculating and fitting fold changes in activity vs controls to sigmoidal curves using a four-parameter logistic model[2].

Animal experiment:

Mice[2]C57Bl/6J mice Food is withdrawn 5 h before dosing, while water is available throughout. A blood sample is taken from the tail tip under local anaesthetic for glucose and insulin measurement. Thereafter, mice are weighed and dosed orally with PSN-GK1 (1 or 10 mg/kg) or vehicle. Blood samples are taken 15, 30, 60, 120 and 240 min after dosing, samples (20 μL) for glucose being taken into disposable micro-pipettes and added to 480 μL haemolysis reagent[2].

References:

[1]. Bertram LS, et al. SAR, pharmacokinetics, safety, and efficacy of glucokinase activating 2-(4-sulfonylphenyl)-N-thiazol-2-ylacetamides: discovery of PSN-GK1. J Med Chem. 2008 Jul 24;51(14):4340-5.
[2]. Fyfe MC, et al. Glucokinase activator PSN-GK1 displays enhanced antihyperglycaemic and insulinotropic actions. Diabetologia. 2007 Jun;50(6):1277-87.