Articles |
From the Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Correspondence to Tetsuhiko Nagao, MD, PhD, Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Maidashi 3-1-1, Fukuoka 812, Japan.
Abstract The effect of an opener (levcromakalim) and a
blocker (glibenclamide) of ATP-sensitive K+
(KATP) channels was investigated in the vertebrobasilar
system of the rabbit. Arterial tension and membrane
potential were measured by the isometric tension recording
method and the microelectrode technique, respectively. Glibenclamide
(10-6 mol/L) depolarized the membrane and
potentiated the contraction to histamine in vertebral arteries. The
sensitivity to the relaxant effects of levcromakalim was in the
following descending order: vertebral>proximal basilar>distal
basilar>superior cerebellar arteries. Vertebral arteries were
50
times more sensitive to levcromakalim than were superior cerebellar
arteries. The relaxation to levcromakalim was abolished by
glibenclamide (10-6 mol/L). Glibenclamide
attenuated vasorelaxation to adenosine in proximal
arteries (vertebral and proximal basilar) but not in superior
cerebellar arteries. Levcromakalim
(7x10-8 mol/L) and adenosine
(10-5 mol/L) induced
glibenclamide-sensitive membrane
hyperpolarization in vertebral arteries but not in
distal basilar arteries. These results suggest that KATP
channels contribute to the determination of resting membrane potential
and resting tone in vertebral arteries. Furthermore, there is a marked
heterogeneity in the sensitivity to an opener of
KATP channels, and the heterogeneity has a
functional link to the mechanism underlying vasorelaxation to
adenosine in the vertebrobasilar system of the rabbit.
Key Words: electrophysiology regional difference hyperpolarization levcromakalim glibenclamide
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