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1 Department of Physiology and Biophysics, Seoul National University College of Medicine, Seoul 110-799; 2 Department of Physiology, College of Medicine, Chosun University, Kwangju 501-759; and 3 Department of Physiology, Sungkyunkwan University College of Medicine, Suwon 440-746, Korea
This study was designed to identify the
single-channel properties and molecular entity of ATP-sensitive
K+ (KATP) channels in guinea pig gastric
myocytes with patch-clamp recording and RT-PCR. Pinacidil and diazoxide
activated KATP currents in a glibenclamide-sensitive
manner. The open probability of channels was enhanced by the
application of 10 µM pinacidil from 0.085 ± 0.04 to 0.20 ± 0.05 (n = 7) and was completely blocked by 10 µM
glibenclamide. Single-channel conductance was 37.3 ± 2.5 pS (n = 4) between
80 and
20 mV in symmetrical
K+ gradient conditions. In inside-out mode,
KATP channels showed no spontaneous openings and were
activated by the application of nucleotide diphosphates to the
cytoplasmic side. These single-channel properties are similar to those
of the nucleotide diphosphate-dependent K+ channels in
vascular smooth muscle, which are composed of Kir6.1 and sulfonylurea
receptor (SUR)2B. RT-PCR demonstrated the presence of Kir6.1, Kir6.2,
and SUR2B in guinea pig stomach smooth muscle cells. These results
suggest that KATP channels in smooth muscle cells of the
guinea pig stomach are composed of Kir6.1 and SUR2B.
adenosine 5'-triphosphate-sensitive potassium channels; Kir6.1-sulfonurea receptor 2B; smooth muscle cells; guinea pig stomach
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