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Expanding clinical evidence is likely to increase payer review of GLP-1 drugs across diabetes and weight management programs
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Opening of ATP-sensitive potassium channels inhibits l-valine induced GLP-1 secretion To investigate whether intracellular metabolism of l-valine leading to the production of ATP and closure of K ATP -channels, subsequently resulting in impaired K + efflux and cellular depolarization, was involved in the mechanisms of l-valine stimulated GLP-1 secretion, we infused the K ATP -channel opener diazoxide (250 M) while stimulating with l-valine (Fig
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