Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1990 Jun;100(2):353–359. doi: 10.1111/j.1476-5381.1990.tb15808.x

Effects of calmodulin antagonists on calcium-activated potassium channels in pregnant rat myometrium.

M Kihira 1, K Matsuzawa 1, H Tokuno 1, T Tomita 1
PMCID: PMC1917429  PMID: 2116204

Abstract

1. The effects of W-7, trifluoperazine, and W-5 on Ca2(+)-activated K(+)-channels were investigated with the inside-out patch-clamp method in smooth muscle cells freshly dispersed from pregnant rat myometrium. These drugs are known to have different potencies as calmodulin antagonists. 2. In the presence of 1 microM Ca2+ on the cytoplasmic side ([Ca2+]i), the fraction of time the channel was open (open probability, Po) was about 0.9 and the calmodulin antagonists (1-30 microM) applied to the cytoplasmic face reduced Po to 0.65-0.55 dose-dependently. In the presence of 0.1-0.16 microM Ca2+, when Po was very low (0.02), calmodulin antagonists increased Po. All antagonists used produced almost identical effects at the same concentration. 3. The probability density function of the open time distribution could be described by the sum of two exponentials. W-7 decreased the time constant of slow component of distribution and at 30 microM the slow component disappeared both at 1 and 0.25 microM [Ca2+]i, reflecting the appearance of flickering channel activity. The probability density function of the closed time distribution could be fitted with three exponentials. The time constants of these components were not significantly altered by W-7. 4. Internally applied calmodulin (1-5 microM) did not produce any significant effect on channel activity. 5. The effects of calmodulin antagonists are considered to be due to a direct action of these compounds on the channel, and suggest that channel activation by Ca2+ is not mediated by calmodulin.

Full text

PDF
357

Selected References

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

  1. 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]
  2. Benham C. D., Bolton T. B., Lang R. J., Takewaki T. The mechanism of action of Ba2+ and TEA on single Ca2+-activated K+ -channels in arterial and intestinal smooth muscle cell membranes. Pflugers Arch. 1985 Feb;403(2):120–127. doi: 10.1007/BF00584088. [DOI] [PubMed] [Google Scholar]
  3. Bregestovski P. D., Bolotina V. M., Serebryakov V. N. Fatty acid modifies Ca2+-dependent potassium channel activity in smooth muscle cells from the human aorta. Proc R Soc Lond B Biol Sci. 1989 Aug 22;237(1288):259–266. doi: 10.1098/rspb.1989.0048. [DOI] [PubMed] [Google Scholar]
  4. Fabiato A. Myoplasmic free calcium concentration reached during the twitch of an intact isolated cardiac cell and during calcium-induced release of calcium from the sarcoplasmic reticulum of a skinned cardiac cell from the adult rat or rabbit ventricle. J Gen Physiol. 1981 Nov;78(5):457–497. doi: 10.1085/jgp.78.5.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Greenberg D. A., Carpenter C. L., Messing R. O. Interaction of calmodulin inhibitors and protein kinase C inhibitors with voltage-dependent calcium channels. Brain Res. 1987 Feb 24;404(1-2):401–404. doi: 10.1016/0006-8993(87)91403-x. [DOI] [PubMed] [Google Scholar]
  6. HODGKIN A. L., KATZ B. The effect of sodium ions on the electrical activity of giant axon of the squid. J Physiol. 1949 Mar 1;108(1):37–77. doi: 10.1113/jphysiol.1949.sp004310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  8. Inoue R., Kitamura K., Kuriyama H. Two Ca-dependent K-channels classified by the application of tetraethylammonium distribute to smooth muscle membranes of the rabbit portal vein. Pflugers Arch. 1985 Oct;405(3):173–179. doi: 10.1007/BF00582557. [DOI] [PubMed] [Google Scholar]
  9. Kishikawa T. Alterations in the properties of the rat myometrium during gestation and post partum. Jpn J Physiol. 1981;31(4):515–536. doi: 10.2170/jjphysiol.31.515. [DOI] [PubMed] [Google Scholar]
  10. Klöckner U., Isenberg G. Calmodulin antagonists depress calcium and potassium currents in ventricular and vascular myocytes. Am J Physiol. 1987 Dec;253(6 Pt 2):H1601–H1611. doi: 10.1152/ajpheart.1987.253.6.H1601. [DOI] [PubMed] [Google Scholar]
  11. Lackington I., Orrego F. Inhibition of calcium-activated potassium conductance of human erythrocytes by calmodulin inhibitory drugs. FEBS Lett. 1981 Oct 12;133(1):103–106. doi: 10.1016/0014-5793(81)80481-4. [DOI] [PubMed] [Google Scholar]
  12. McCann J. D., Welsh M. J. Calcium-activated potassium channels in canine airway smooth muscle. J Physiol. 1986 Mar;372:113–127. doi: 10.1113/jphysiol.1986.sp016000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. McCann J. D., Welsh M. J. Neuroleptics antagonize a calcium-activated potassium channel in airway smooth muscle. J Gen Physiol. 1987 Feb;89(2):339–352. doi: 10.1085/jgp.89.2.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Neher E., Steinbach J. H. Local anaesthetics transiently block currents through single acetylcholine-receptor channels. J Physiol. 1978 Apr;277:153–176. doi: 10.1113/jphysiol.1978.sp012267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Okada Y., Yada T., Ohno-Shosaku T., Oiki S. Evidence for the involvement of calmodulin in the operation of Ca-activated K channels in mouse fibroblasts. J Membr Biol. 1987;96(2):121–128. doi: 10.1007/BF01869238. [DOI] [PubMed] [Google Scholar]
  16. Osa T., Fujino T. Electrophysiological comparison between the longitudinal and circular muscles of the rat uterus during the estrous cycle and pregnancy. Jpn J Physiol. 1978;28(2):197–209. doi: 10.2170/jjphysiol.28.197. [DOI] [PubMed] [Google Scholar]
  17. Pape L., Kristensen B. I. A calmodulin activated Ca2+-dependent K+ channel in human erythrocyte membrane inside-out vesicles. Biochim Biophys Acta. 1984 Feb 29;770(1):1–6. doi: 10.1016/0005-2736(84)90065-8. [DOI] [PubMed] [Google Scholar]

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

RESOURCES