Korean J Physiol Pharmacol.
1999 Aug;3(4):439-445.
Effect of imipramine on calcium utilization of single cells isolated from canine detruso
- Affiliations
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- 1Department of Pharmacology, College of Medicine, Yeungnam University, 317-1 Daemyung Dong, Taegu, 705-717 South Korea.
- 2Department of Pharmacology, College of Pharmacy, Chungang University, Seoul 156-756, Korea.
Abstract
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This study is to investigate the mechanism of inhibitory effect of
imipramine on the calcium utilization in single cells isolated from
canine detrusor. 2 mm thick smooth muscle chops were incubated in 0.12%
collagenase solution at 36degreeC, and aerated with 95% O2/5% CO2, and
then cell suspension was examined Acetylcholine (ACh) evoked a
concentration-dependent contraction of the isolated detrusor cells in
normal physiologic salt solution (PSS), and the ACh-induced contraction
was significantly inhibited by imipramine. In Ca2+-free PSS,
ACh-induced contraction was less than those in normal PSS and it was
not affected by the pretreatment with imipramine. Ca2+-induced
contraction in Ca2+-free PSS was supressed by imipramine, but addition
of A 23187, a calcium ionophore, overcomed the inhibitory effect of
imipramine. High potassium-depolarization (40 mM KCl) evoked cell
contraction, which was inhibited by imipramine. Caffeine, a releasing
agent of the stored Ca2+ from sarcoplasmic reticulum, evoked a
contraction of the cells that was not blocked by the pretreatment with
imipramine. These results suggest that imipramine inhibits the influx
of calcium in the detrusor cells through both the receptor-operated-
and voltage-gated-calcium channels, but does not affect the release of
calcium from intracellular storage site.