Simultaneous recordings of glucose dependent electrical activity and ATP-regulated K+-currents in isolated mouse pancreatic β-cells
Membrane potential and membrane currents were recorded from single mouse pancreatic β-
cells using the perforated patch whole-cell recording technique at 30° C. Single β-cells
maintained in primary tissue culture exhibited glucose-dependent electrical activity similar to
that reported for freshly isolated intact islets. The resting input conductance (5.1±0.9 nS) was
determined by ATP-regulated K+(K ATP) channels as it was blocked by 1 mM tolbutamide. 8
mM glucose decreased the input conductance by 80%. The input conductance at− 70 mV …
cells using the perforated patch whole-cell recording technique at 30° C. Single β-cells
maintained in primary tissue culture exhibited glucose-dependent electrical activity similar to
that reported for freshly isolated intact islets. The resting input conductance (5.1±0.9 nS) was
determined by ATP-regulated K+(K ATP) channels as it was blocked by 1 mM tolbutamide. 8
mM glucose decreased the input conductance by 80%. The input conductance at− 70 mV …
Abstract
Membrane potential and membrane currents were recorded from single mouse pancreatic β-cells using the perforated patch whole-cell recording technique at 30 °C. Single β-cells maintained in primary tissue culture exhibited glucose-dependent electrical activity similar to that reported for freshly isolated intact islets. The resting input conductance (5.1±0.9 nS) was determined by ATP-regulated K+ (KATP) channels as it was blocked by 1 mM tolbutamide. 8 mM glucose decreased the input conductance by 80%. The input conductance at −70 mV was of a similar value during the plateau phase and during the silent phase of electrical activity in 8 mM glucose. This suggests that oscillations of KATP channel activity do not underlie the slow waves.
Elsevier
