Korean J Physiol Pharmacol.
2000 Feb;4(1):33-40.
The effect of NO donor on contraction, cytosolic Ca2+ level and ionic currents in guinea-pig ileal smooth muscle
- Affiliations
-
- 1Department of Physiology, Yonsei University College of Medicine, 134
Shinchon-dong, Seodaemun-gu, Seoul, South Korea.
Abstract
- This study was designed to clarify the mechanism of the inhibitory
action of a nitric oxide (NO) donor, 3-morpholino-sydnonimine (SIN-1),
on contraction, cytosolic Ca2+ level ((Ca2+)i), and ionic currents in
guinea-pig ileum. SIN-1 (0.01~100 micrometer) inhibited 25 mM KCl- or
histamine (10 micrometer)-induced contraction in a concentration-dependent
manner. SIN-1 reduced both the 25 mM KCl- and the histamine-stimulated
increases in muscle tension in parallel with decreased (Ca2+)i. Using
the patch clamp technique with a holding potential of -60 mV, SIN-1 (10
micrometer) decreased peak Ba currents (IBa) by 30.9+/-5.4% (n=6) when voltage
was stepped from -60 mV to +10 mV and this effect was blocked by ODQ (1
micrometer), a soluble guanylyl cyclase inhibitor. Cu/Zn SOD (100 U/ml), the
free radical scavenger, had little effect on basal IBa, and SIN-1 (10
micrometer) inhibited peak IBa by 32.4+/-5.8% (n=5) in the presence of Cu/Zn
SOD. In a cell clamped at a holding-potential of -40 mV, application of
10 micrometer histamine induced an inward current. The histamine-induced
inward current was markedly and reversibly inhibited by 10 micrometer SIN-1,
and this effect was abolished by ODQ (1 micrometer). In addition, SIN-1
markedly increased the depolarization-activated outward K+ currents in
the all potential ranges. We concluded that SIN-1 inhibits smooth
muscle contraction mainly by decreasing (Ca2+)i resulted from the
inhibition of L-type Ca2+ channels and the inhibition of nonselective
cation currents and/or by the activation of K+ currents via a
cGMP-dependent pathway.