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• W2034772537 abstract "ATP-sensitive potassium channels (K ATP ) are involved in a diverse array of physiologic functions including protection of tissue against ischemic insult, regulation of vascular tone, and modulation of insulin secretion. To improve our understanding of the role of K ATP in these processes, we used a gene-targeting strategy to generate mice with a disruption in the muscle-specific K ATP regulatory subunit, SUR2. Insertional mutagenesis of the Sur2 locus generated homozygous null ( Sur2 −/− ) mice and heterozygote ( Sur2 +/− ) mice that are viable and phenotypically similar to their wild-type littermates to 6 weeks of age despite, respectively, half or no SUR2 mRNA expression or channel activity in skeletal muscle or heart. Sur2 −/− animals had lower fasting and fed serum glucose, exhibited improved glucose tolerance during a glucose tolerance test, and demonstrated a more rapid and severe hypoglycemia after administration of insulin. Enhanced glucose use was also observed during in vivo hyperinsulinemic euglycemic clamp studies during which Sur2 −/− mice required a greater glucose infusion rate to maintain a target blood glucose level. Enhanced insulin action was intrinsic to the skeletal muscle, as in vitro insulin-stimulated glucose transport was 1.5-fold greater in Sur2 −/− muscle than in wild type. Thus, membrane excitability and K ATP activity, to our knowledge, seem to be new components of the insulin-stimulated glucose uptake mechanism, suggesting possible future therapeutic approaches for individuals suffering from diabetes mellitus." @default.
• W2034772537 created "2016-06-24" @default.
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• W2034772537 date "2001-09-18" @default.
• W2034772537 modified "2023-09-23" @default.
• W2034772537 title "Disruption of <i>Sur2</i> -containing K _ATP channels enhances insulin-stimulated glucose uptake in skeletal muscle" @default.
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• W2034772537 doi "https://doi.org/10.1073/pnas.201390398" @default.
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