Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1993 Jul;109(3):793–801. doi: 10.1111/j.1476-5381.1993.tb13644.x

Pharmacological characterization of muscarinic receptor-activated cation channels in guinea-pig ileum.

S Chen 1, R Inoue 1, Y Ito 1
PMCID: PMC2175634  PMID: 7689404

Abstract

1. The pharmacological properties of cationic currents activated by acetylcholine (ACh) (Icat) in guinea-pig ileal smooth muscle cells were investigated, with conventional single patch electrode or nystatin-perforated whole-cell recording. Cs-aspartate was used as the internal solution to allow selective measurement of Icat. 2. Well-known K channel blockers, tetraethylammonium (TEA), 4-aminopyridine (4-AP), procaine and quinine as well as a Ca releasing agent, caffeine, all produced concentration-dependent inhibition of Icat with rapid onset (time constant approximately 100 ms), when applied externally. The recovery from the inhibition on washout also occurred rapidly in the order of 100 ms except in the case of quinine. Approximate values of the half inhibitory concentrations (IC50) were 10 nM for TEA and caffeine, 1-5 mM for 4-AP and procaine, and 1 microM for quinine. The mode of inhibition was voltage-dependent, i.e., depolarization relieved the inhibition with no change in reversal potential. 3. Externally applied diphenylamine-2-carboxylate (DPC) derivatives, DCDPC and flufenamic acid, produced potent inhibition of Icat at micromolar concentrations (IC50s were < 30 microM for DCDPC and 32 microM for flufenamic acid). The onset of and recovery from inhibition occurred slowly and the degree of inhibition depended on the membrane potential only weakly, without any discernible change in the reversal potential. 4. All of the above-tested drugs exhibited comparable inhibitory actions on the voltage-dependent Ca current in the concentration ranges effective at inhibiting Icat. However, amongst them, quinine and flufenamic acid seemed to have several-fold better selectivity for the Icat channel than for the voltage-dependent Ca channel.(ABSTRACT TRUNCATED AT 250 WORDS)

Full text

PDF
793

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bean B. P. ATP-activated channels in rat and bullfrog sensory neurons: concentration dependence and kinetics. J Neurosci. 1990 Jan;10(1):1–10. doi: 10.1523/JNEUROSCI.10-01-00001.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beech D. J., Bolton T. B. A voltage-dependent outward current with fast kinetics in single smooth muscle cells isolated from rabbit portal vein. J Physiol. 1989 May;412:397–414. doi: 10.1113/jphysiol.1989.sp017623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beech D. J., Bolton T. B. Two components of potassium current activated by depolarization of single smooth muscle cells from the rabbit portal vein. J Physiol. 1989 Nov;418:293–309. doi: 10.1113/jphysiol.1989.sp017841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Benham C. D., Bolton T. B., Lang R. J., Takewaki T. Calcium-activated potassium channels in single smooth muscle cells of rabbit jejunum and guinea-pig mesenteric artery. J Physiol. 1986 Feb;371:45–67. doi: 10.1113/jphysiol.1986.sp015961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bolton T. B. Mechanisms of action of transmitters and other substances on smooth muscle. Physiol Rev. 1979 Jul;59(3):606–718. doi: 10.1152/physrev.1979.59.3.606. [DOI] [PubMed] [Google Scholar]
  6. Ehara T., Noma A., Ono K. Calcium-activated non-selective cation channel in ventricular cells isolated from adult guinea-pig hearts. J Physiol. 1988 Sep;403:117–133. doi: 10.1113/jphysiol.1988.sp017242. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gögelein H., Capek K. Quinine inhibits chloride and nonselective cation channels in isolated rat distal colon cells. Biochim Biophys Acta. 1990 Aug 24;1027(2):191–198. doi: 10.1016/0005-2736(90)90084-2. [DOI] [PubMed] [Google Scholar]
  8. Gögelein H., Dahlem D., Englert H. C., Lang H. J. Flufenamic acid, mefenamic acid and niflumic acid inhibit single nonselective cation channels in the rat exocrine pancreas. FEBS Lett. 1990 Jul 30;268(1):79–82. doi: 10.1016/0014-5793(90)80977-q. [DOI] [PubMed] [Google Scholar]
  9. Gögelein H., Pfannmüller B. The nonselective cation channel in the basolateral membrane of rat exocrine pancreas. Inhibition by 3',5-dichlorodiphenylamine-2-carboxylic acid (DCDPC) and activation by stilbene disulfonates. Pflugers Arch. 1989 Jan;413(3):287–298. doi: 10.1007/BF00583543. [DOI] [PubMed] [Google Scholar]
  10. Horn R., Marty A. Muscarinic activation of ionic currents measured by a new whole-cell recording method. J Gen Physiol. 1988 Aug;92(2):145–159. doi: 10.1085/jgp.92.2.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Huettner J. E., Bean B. P. Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: selective binding to open channels. Proc Natl Acad Sci U S A. 1988 Feb;85(4):1307–1311. doi: 10.1073/pnas.85.4.1307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Iino M. Calcium-induced calcium release mechanism in guinea pig taenia caeci. J Gen Physiol. 1989 Aug;94(2):363–383. doi: 10.1085/jgp.94.2.363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Imaizumi Y., Muraki K., Watanabe M. Characteristics of transient outward currents in single smooth muscle cells from the ureter of the guinea-pig. J Physiol. 1990 Aug;427:301–324. doi: 10.1113/jphysiol.1990.sp018173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Inoue R. Effect of external Cd2+ and other divalent cations on carbachol-activated non-selective cation channels in guinea-pig ileum. J Physiol. 1991 Oct;442:447–463. doi: 10.1113/jphysiol.1991.sp018802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Inoue R., Isenberg G. Acetylcholine activates nonselective cation channels in guinea pig ileum through a G protein. Am J Physiol. 1990 Jun;258(6 Pt 1):C1173–C1178. doi: 10.1152/ajpcell.1990.258.6.C1173. [DOI] [PubMed] [Google Scholar]
  16. Inoue R., Isenberg G. Effect of membrane potential on acetylcholine-induced inward current in guinea-pig ileum. J Physiol. 1990 May;424:57–71. doi: 10.1113/jphysiol.1990.sp018055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Inoue R., Isenberg G. Intracellular calcium ions modulate acetylcholine-induced inward current in guinea-pig ileum. J Physiol. 1990 May;424:73–92. doi: 10.1113/jphysiol.1990.sp018056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Inoue R., Kitamura K., Kuriyama H. Acetylcholine activates single sodium channels in smooth muscle cells. Pflugers Arch. 1987 Sep;410(1-2):69–74. doi: 10.1007/BF00581898. [DOI] [PubMed] [Google Scholar]
  19. Inoue R., Kuriyama H. Dual regulation of cation-selective channels by muscarinic and alpha 1-adrenergic receptors in the rabbit portal vein. J Physiol. 1993 Jun;465:427–448. doi: 10.1113/jphysiol.1993.sp019685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Inoue R., Kuriyama H. Stabilized recording of ACh activated non-selective cationic conductance in guinea-pig ileal smooth muscle using a nystatin-permeabilized whole-cell recording. Jpn J Pharmacol. 1992;58 (Suppl 2):345P–345P. [PubMed] [Google Scholar]
  21. Itoh T., Kuriyama H., Suzuki H. Excitation--contraction coupling in smooth muscle cells of the guinea-pig mesenteric artery. J Physiol. 1981 Dec;321:513–535. doi: 10.1113/jphysiol.1981.sp014000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Komori S., Bolton T. B. Role of G-proteins in muscarinic receptor inward and outward currents in rabbit jejunal smooth muscle. J Physiol. 1990 Aug;427:395–419. doi: 10.1113/jphysiol.1990.sp018178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ohya Y., Kitamura K., Kuriyama H. Cellular calcium regulates outward currents in rabbit intestinal smooth muscle cell. Am J Physiol. 1987 Apr;252(4 Pt 1):C401–C410. doi: 10.1152/ajpcell.1987.252.4.C401. [DOI] [PubMed] [Google Scholar]
  24. Okabe K., Kitamura K., Kuriyama H. Features of 4-aminopyridine sensitive outward current observed in single smooth muscle cells from the rabbit pulmonary artery. Pflugers Arch. 1987 Aug;409(6):561–568. doi: 10.1007/BF00584654. [DOI] [PubMed] [Google Scholar]
  25. Poronnik P., Ward M. C., Cook D. I. Intracellular Ca2+ release by flufenamic acid and other blockers of the non-selective cation channel. FEBS Lett. 1992 Jan 27;296(3):245–248. doi: 10.1016/0014-5793(92)80296-s. [DOI] [PubMed] [Google Scholar]
  26. Siemer C., Gögelein H. Activation of nonselective cation channels in the basolateral membrane of rat distal colon crypt cells by prostaglandin E2. Pflugers Arch. 1992 Mar;420(3-4):319–328. doi: 10.1007/BF00374465. [DOI] [PubMed] [Google Scholar]
  27. Smirnov S. V., Aaronson P. I. Ca(2+)-activated and voltage-gated K+ currents in smooth muscle cells isolated from human mesenteric arteries. J Physiol. 1992 Nov;457:431–454. doi: 10.1113/jphysiol.1992.sp019386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Sturgess N. C., Hales C. N., Ashford M. L. Calcium and ATP regulate the activity of a non-selective cation channel in a rat insulinoma cell line. Pflugers Arch. 1987 Aug;409(6):607–615. doi: 10.1007/BF00584661. [DOI] [PubMed] [Google Scholar]
  29. Vogalis F., Sanders K. M. Cholinergic stimulation activates a non-selective cation current in canine pyloric circular muscle cells. J Physiol. 1990 Oct;429:223–236. doi: 10.1113/jphysiol.1990.sp018253. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES