Korean J Physiol Pharmacol.
1998 Jun;2(3):353-359.
Inhibitory effect of caffeine on carbachol-induced nonselective
cationic current in guinea-pig gastric myocytes
- Affiliations
-
- 1Department of Physiology & Biophysics, Seoul National University College of Medicine, Seoul 110-799, Korea.
- 2Heart Research Institute, Seoul National University Medical Research Center, Korea.
- 3Department of Physiology, Chungbuk National University College of Medicine, Korea.
Abstract
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In gastrointestinal smooth muscle, muscarinic stimulation by carbachol
(CCh) activates nonselective cation channel current (ICCh) which is
facilitated by intracellular (Ca2+) increase. Caffeine is widely used
in experiments to mobilize Ca2+ from intracellular stores. This study
shows a strong inhibitory effect of caffeine on ICCh in guinea-pig
gastric myocyte. In this study, the underlying mechanism of the
inhibitory effect of caffeine was investigated. ICCh was completely
suppressed by the addition of caffeine (10 mM) to the superfusing
solution. Inhibition of ICCh by caffeine was not related to the
intracellular cAMP accumulation which was expected from the
phosphodiesterase-inhibiting effect of caffeine. The blockade of
InsP3-induced Ca2+ release by heparin had no significant effects on the
activation of ICCh. When the same cationic current had been induced by
intracellular dialysis of GTP(gammaS) in order to bypass the muscarinic
receptor, the inhibitory effect of caffeine was significantly
attenuated. The results of this study indicate that both intracellular
signalling pathways for ICCh, proximal and distal to G-protein
activation, are suppressed by caffeine. A major inhibition was observed
at the proximal level.