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- W4313333191 abstract "Type 2 diabetes (T2D) is a global health problem characterised by chronic hyperglycaemia due to inadequate insulin secretion. Because glucose must be metabolised to stimulate insulin release it was initially argued that drugs that stimulate glucokinase (the first enzyme in glucose metabolism) would enhance insulin secretion in diabetes. However, in the long term, glucokinase activators have been largely disappointing. Recent studies show it is hyperactivation of glucose metabolism, not glucose itself, that underlies the progressive decline in beta-cell function in diabetes. This perspective discusses if glucokinase activators exacerbate this decline (by promoting glucose metabolism) and, counterintuitively, if glucokinase inhibitors might be a better therapeutic strategy for preserving beta-cell function in T2D." @default.
- W4313333191 created "2023-01-06" @default.
- W4313333191 creator A5017075486 @default.
- W4313333191 creator A5051240015 @default.
- W4313333191 creator A5063776275 @default.
- W4313333191 date "2023-02-01" @default.
- W4313333191 modified "2023-10-01" @default.
- W4313333191 title "Glucokinase activity in diabetes: too much of a good thing?" @default.
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- W4313333191 doi "https://doi.org/10.1016/j.tem.2022.12.007" @default.
- W4313333191 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36586779" @default.
- W4313333191 hasPublicationYear "2023" @default.
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