Abstract
1. Whole-cell current-clamp recordings demonstrate that leptin (0.3-10 nm) hyperpolarizes CRI-G1 insulin-secreting cells. This effect is slow on onset and is not reversed on washout of the leptin. 2. Voltage-clamp recordings indicate that leptin activates a potassium conductance in the presence of intracellular ATP (5 mm), but has not effect in its absence. Following activation of ATP-sensitive K+ (KATP) current by diazoxide (0.2 mm), addition of leptin did not alter cell membrane potential or potassium current further. 3. The leptin-induced hyperpolarization and increased potassium conductance are completely inhibited by the application of the sulphonylureas tolbutamide (100 microM) and glibenclamide (0.5 microM). 4. Cell-attached and inside-out single-channel recordings indicate that leptin activates tolbutamide-sensitive KATP channels in CRI-G1 insulin-secreting cells.
Original language | English |
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Pages (from-to) | 527-35 |
Number of pages | 9 |
Journal | Journal of Physiology |
Volume | 504 |
Issue number | ( Pt 3) |
Publication status | Published - 1 Nov 1997 |
Keywords
- Animals
- Ion Channel Gating
- Electrophysiology
- Insulin
- Potassium Channels
- Rats
- Leptin
- Hypoglycemic Agents
- Patch-Clamp Techniques
- Biotransformation
- Membrane Potentials
- Proteins
- Tolbutamide
- Adenosine Triphosphate
- Cell Line