Korean J Physiol Pharmacol.
2000 Dec;4(6):463-469.
Relaxant effect of 4-aminopyridine on the mesenteric artery of rat
- Affiliations
-
- 1Department of Physiology, College of Medicine, Konyang University,
26 Nae-dong, Nonsan, Chungnam, South Korea.
sehkim@kytis.konyang.ac.kr
Abstract
- It has been well known that 4-aminopyridine (4-AP) has an excitatory
effect on vascular smooth muscle due to causing membrane depolarization
by blocking K+-channel. However, we observed that 4-AP had an
inhibitory effect on the mesenteric artery of rat. Therefore, we
investigated the mechanism of 4-AP-induced vasorelaxation. The
mesenteric arcuate artery and its branches were isolated and cut into
ring. The ring segment was immersed in HEPES-buffered solution and its
isometric tension was measured. 4-AP (0.1 ~ 10 mM) induced a
concentration-dependent relaxation, which was unaffected by NO synthase
inhibitor, NG-nitro-L-arginine methylester (100 micrometer) or soluble
guanylate cyclase inhibitor, methylene blue (10 micrometer). Glibenclamide (10
micrometer), ATP-sensitive K+ channel blocker, did not exert any effect on the
4-AP-induced vasorelaxation. 4-AP relaxed the sustained contraction
induced by 100 mM K+ or Ca2+ ionophore, A23187 (10 micrometer) in a
dose-dependent manner. In addition, 4-AP significantly decreased the
phasic contractile response to norepinephrine in the absence of
extracellular Ca2+. However, 4-AP did not block the 45Ca influx of rat
aorta. From the above results, we suggest that 4-AP may not block the
Ca2+ influx through Ca2+-channel, but act as a nonspecific vasorelaxant
in arterial smooth muscle.