Journal of Clinical Investigation · 1996 · 69 citations · 22 references
Life SciencesEndocrinologyPhysiologyElectrophysiologyIon Channel BiophysicsSignal TransductionCalcium SignalingDiabetes MellitusIntracellular Calcium SignalingIon Channel PhysiologyIon Channel RegulationIon ChannelsGlucose-dependent Insulin SecretionGlucose-stimulated Insulin SecretionMembrane DepolarizationPancreatic Beta-cell SecretionPancreatic Islet CellsPatch-clamp RecordingVoltage-gated Calcium ChannelsWhole-cell Patch Clamp
In genetically occurring non-insulin-dependent diabetes mellitus (NIDDM) model rats (GK rats), the activities of L- and T-type Ca2+ channels in pancreatic beta cells are found to be augmented, by measuring the Ba2+ currents via these channels using whole-cell patch-clamp technique, while the patterns of the current-voltage curves are indistinguishable. The hyper-responsiveness of insulin secretion to nonglucose depolarizing stimuli observed in NIDDM beta cells could be the result, therefore, of increased voltage-dependent Ca2+ channel activity. Perforated patch-clamp recordings reveal that the augmentation of L-type Ca2+ channel activity by glucose is markedly less pronounced in GK beta cells than in control beta cells, while glucose-induced augmentation of T-type Ca2+ channel activity is observed neither in the control nor in the GK beta cells. This lack of glucose-induced augmentation of L-type Ca2+ channel activity in GK beta cells might be causatively related to the selective impairment of glucose-induced insulin secretion in NIDDM beta cells, in conjunction with an insufficient plasma membrane depolarization due to impaired closure of the ATP-sensitive K+ channels caused by the disturbed intracellular glucose metabolism in NIDDM beta cells.
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A New in Vitro Model for the Study of Pancreatic A and B Cells*
Daniël Pipeleers, Pieter In 'T Veld, M. Van De Winkel et al. · Endocrinology · 1985 · 342 citations