Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1993 Aug;468:297–310. doi: 10.1113/jphysiol.1993.sp019772

Characterization of an outward potassium current in canine jejunal circular smooth muscle and its activation by fenamates.

G Farrugia 1, J L Rae 1, J H Szurszewski 1
PMCID: PMC1143827  PMID: 8254511

Abstract

1. A perforated patch clamp technique was used to study an outward potassium current in freshly dissociated circular smooth muscle cells of the canine jejunum. 2. A voltage-dependent outward current was identified which was highly potassium selective, weakly holding voltage sensitive, increased its open probability at -65 mV, and reached unit open probability at +5 mV. 3. Quinidine (0.1-1 mM) and tetraethylammonium ion (TEA) (10-50 mM), blocked the potassium current in a dose-dependent manner. Blockade of the outward potassium current was accompanied by membrane depolarization which reversed on removal of the blocker from the bathing solution. 4. Mefenamic and flufenamic acids, non-steroidal anti-inflammatory agents in the fenamate group, were potent activators of the current. Activation was accompanied by hyperpolarization of the membrane with a mean shift in the membrane voltage of 22 mV. 5. It was concluded that the outward potassium current is a major regulator of the resting membrane voltage in isolated circular smooth muscle cells of the canine jejunum. Fenamates activated this current with potentially profound effects on cellular excitability.

Full text

PDF
297

Selected References

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

  1. Cooper K., Gates P., Rae J. L., Dewey J. Electrophysiology of cultured human lens epithelial cells. J Membr Biol. 1990 Sep;117(3):285–298. doi: 10.1007/BF01868458. [DOI] [PubMed] [Google Scholar]
  2. Daniel E. E. The electrical activity of the alimentary tract. Am J Dig Dis. 1968 Apr;13(4):297–319. doi: 10.1007/BF02233006. [DOI] [PubMed] [Google Scholar]
  3. El-Sharkaway T. Y., Daniel E. E. Ionic mechanisms of intestinal electrical control activity. Am J Physiol. 1975 Nov;229(5):1287–1298. doi: 10.1152/ajplegacy.1975.229.5.1287. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. Hara Y., Kubota M., Szurszewski J. H. Electrophysiology of smooth muscle of the small intestine of some mammals. J Physiol. 1986 Mar;372:501–520. doi: 10.1113/jphysiol.1986.sp016022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hille B. Potassium channels in myelinated nerve. Selective permeability to small cations. J Gen Physiol. 1973 Jun;61(6):669–686. doi: 10.1085/jgp.61.6.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Knauf P. A., Spinelli L. J., Mann N. A. Flufenamic acid senses conformation and asymmetry of human erythrocyte band 3 anion transport protein. Am J Physiol. 1989 Aug;257(2 Pt 1):C277–C289. doi: 10.1152/ajpcell.1989.257.2.C277. [DOI] [PubMed] [Google Scholar]
  8. 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]
  9. Rae J. L., Farrugia G. Whole-cell potassium current in rabbit corneal epithelium activated by fenamates. J Membr Biol. 1992 Jul;129(1):81–97. doi: 10.1007/BF00232057. [DOI] [PubMed] [Google Scholar]
  10. Rae J., Cooper K., Gates P., Watsky M. Low access resistance perforated patch recordings using amphotericin B. J Neurosci Methods. 1991 Mar;37(1):15–26. doi: 10.1016/0165-0270(91)90017-t. [DOI] [PubMed] [Google Scholar]
  11. Thornbury K. D., Ward S. M., Sanders K. M. Participation of fast-activating, voltage-dependent K currents in electrical slow waves of colonic circular muscle. Am J Physiol. 1992 Jul;263(1 Pt 1):C226–C236. doi: 10.1152/ajpcell.1992.263.1.C226. [DOI] [PubMed] [Google Scholar]
  12. White M. M., Aylwin M. Niflumic and flufenamic acids are potent reversible blockers of Ca2(+)-activated Cl- channels in Xenopus oocytes. Mol Pharmacol. 1990 May;37(5):720–724. [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES