<P> 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<SUP></SUP>-channel. However, we observed that 4-AP had an inhibitor...
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https://www.riss.kr/link?id=A105379418
2000
-
518
SCIE,SCOPUS,KCI등재
학술저널
455-461(7쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P> 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<SUP></SUP>-channel. However, we observed that 4-AP had an inhibitor...
<P> 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<SUP></SUP>-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, N<SUP>G</SUP>-nitro-L-arginine methylester (100μM) or soluble guanylate cyclase inhibitor, methylene blue (10μM). Glibenclamide (10μM), ATP-sensitive K<SUP></SUP> channel blocker, did not exert any effect on the 4-AP-induced vasorelaxation. 4-AP relaxed the sustained contraction induced by 100 mM K<SUP></SUP> or Ca<SUP>2</SUP> ionophore, A23187 (10μM) in a dose-dependent manner. In addition, 4-AP significantly decreased the phasic contractile response to norepinephrine in the absence of extracellular Ca<SUP>2</SUP>. However, 4-AP did not block the <SUP>45</SUP>Ca influx of rat aorta. From the above results, we suggest that 4-AP may not block the Ca<SUP>2</SUP> influx through Ca<SUP>2</SUP>-channel, but act as a nonspecific vasorelaxant in arterial smooth muscle.