Eliasson, L, Renstrom, E, Ammala, C, Berggren, PO, Bertorello, AM, Bokvist, K, Chibalin, A, Deeney, JT, Flatt, Peter, Gabel, J, Gromada, J, Larsson, O, Lindstrom, P, Rhodes, CJ and Rorsman, P (1996) PKC-dependent stimulation of exocytosis by sulfonylureas in pancreatic beta cells. SCIENCE, 271 (5250). pp. 813-815. [Journal article]
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Hypoglycemic sulfonylureas represent a group of clinically useful antidiabetic compounds that stimulate insulin secretion from pancreatic beta cells. The molecular mechanisms involved are not fully understood but are believed to involve inhibition of potassium channels sensitive to adenosine triphosphate (K-ATP channels) in the beta cell membrane, causing membrane depolarization, calcium influx, and activation of the secretory machinery. In addition to these effects, sulfonylureas also promoted exocytosis by direct interaction with the secretory machinery not involving closure of the plasma membrane K-ATP channels. This effect was dependent on protein kinase C (PKC) and was observed at therapeutic concentrations of sulfonylureas, which suggests that it contributes to their hypoglycemic action in diabetics.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Life and Health Sciences|
Faculty of Life and Health Sciences > School of Biomedical Sciences
|Research Institutes and Groups:||Biomedical Sciences Research Institute|
Biomedical Sciences Research Institute > Diabetes
|Deposited By:||Professor Peter Flatt|
|Deposited On:||08 Jan 2010 13:17|
|Last Modified:||09 May 2016 10:48|
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