Properties of the apamin-sensitive component of Ca2+-dependent K+ current in smooth muscle cells of the guinea pigtaenia coli
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Abstract
With the help of a standard voltage-clamp technique, we investigated transmembrane ion currents in isolated smooth muscle cells of the guinea pigtaenia coli. In Ca2+-dependent K+ current, we identified and studied the properties of an apamin-sensitive voltage-independent component carried through the channels of low conductance (in many publications called small conductance,I SK(Ca)). This component did not show the temporal inactivation;I SK(Ca) was insensitive to the action of 4 mM tetraethylammonium, but was completely blocked by 500 nM of apamin. It was shown thatI SK(Ca) is very sensitive to changes in the intracellular Ca2+ concentration ([Ca2+] i ): a decrease in [Ca2+] i up to 50 nM resulted in the almost complete blockade of the current. The entry of Ca ions into a cell from the external solution through the voltage-operated Ca2+ channels of L-type was not an obligatory condition for activation ofI SK(Ca). The current-voltage relationship forI SK(Ca) had a maximum within the voltage range of +20 to +50 mV.
Keywords
smooth muscle cells Ca2+-dependent K+ channels intracellular Ca2+ concentration apamin tetraethylammoniumPreview
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- 1.A. V. Zholos, V. A. Bouryi, and M. F. Shuba “Components of transmembrane ion current of the electroexcitable membrane of smooth muscle cells,”Biol. Membrany,3, No. 8, 804–815 (1986).Google Scholar
- 2.Y. Yamamoto, S. L. Hu, and C. Y. Kao, “Outward current in single smooth muscle cells of the guinea pigtaenia coli,”Gen. J. Physiol.,93, No. 3, 551–564 (1989).CrossRefGoogle Scholar
- 3.S. L. Hu, Y. Yamamoto, and C. Y. Kao, “Permeation, selectivity, and blockade of the Ca2+-activated potassium channel of the guinea pigtaenia coli myocyte,”Gen. J. Physiol. 94, No. 5, 849–862 (1989).CrossRefGoogle Scholar
- 4.A. V. Povstyan, A. V. Zima, V. L. Reznikov, et al., “Components of depolarization-induced transmembrane ion current in isolated smooth muscle cells of the guinea pigtaenia coli,”Neirofiziologiya/Neurophysiology,29, Nos. 4/5, 340–350 (1997).Google Scholar
- 5.A. V. Povstyan, A. V. Zima, M. I. Harhun, and M. F. Shuba, “Properties of a charibdotoxin-sensitive component of Ca2+-dependent K+ current in smooth muscle cells of the guinea pigtaenia coli,”Neirofiziologiya/Neurophysiology,32, No. 1, 3–10, (2000).Google Scholar
- 6.M. Hugues, H. Schmid, G. Romey, et al., “The Ca2+-dependent slow K+ conductance in cultured rat muscle cells: characterization with apamin,”EMBO J.,1, 1039–1042 (1982).PubMedGoogle Scholar
- 7.A. L. Blatz and K. L. Magleby, “Single apamin-blocked Ca-activated K+ channels of low conductance in cultured rat skeletal muscle,”Nature,323, 718–720 (1986).PubMedCrossRefGoogle Scholar
- 8.T. Capiod and D. C. Ogden, “The properties of calcium-activated potassium ion channels in guinea-pig isolated hepatocytes,”J. Physiol.,409, 285–295 (1989).PubMedGoogle Scholar
- 9.H. S. Gagov, D. B. Duridanova, and K. K. Boev, “Participation of calcium, released from the IP3-sensitive Ca-store, in activation of Ca-dependent potassium conductance of ileal smooth muscle cells,”Gen. Physiol. Biophys.,12, 199–211 (1993).PubMedGoogle Scholar
- 10.F. Vogalis and R. K. Goyal, “Activation of small conductance Ca2+-dependent K+ channels by purinergic agonists in smooth muscle cells of the mouse ileum,”J. Physiol.,502, No. 3, 497–508 (1997).PubMedCrossRefGoogle Scholar
- 11.F. Vogalis, Y. Zhang, and R. K. Goyal, “An intermediate conductance K+ channel in the cell membrane of mouse intestinal smooth muscle,”Biochim. Biophys. Acta,1371, No. 2, 309–316 (1998).PubMedCrossRefGoogle Scholar
- 12.S. D. Koh, G. M. Dick, and K. M. Sanders, “Small-conductance Ca2+-dependent K+ channels activated by ATP in murine colonic smooth muscle,”Am. J. Physiol.,273, No. 6, C2010-C2021 (1997).PubMedGoogle Scholar
- 13.A. V. Zima, A. V. Povstyan, and M. F. Shuba, “Ca2+-dependent K+ channels of big conductance in the membrane of smooth muscle cells of the guinea pigtaenia coli,”Vestn. Kar’kov Univ., Ser. Biophys. Vestn., No. 466, Issue 5, 47–51 (1999).Google Scholar
- 14.O. P. Hamill, A. Marty, E. Neher, et al., “Improved patch-clamp techniques for high-resolution current recording from cell-free membrane patches,”Pflügers Arch.,391, No. 1, 85–100 (1981).PubMedCrossRefGoogle Scholar
- 15.A. V. Zima, A. É. Belevich, Ya. D. Tsytsyura, and M. F. Shuba, “Effect of nitric oxide on Ca2+ and Ca2+-activated K+ channels in smooth muscle cells of the guinea pigtaenia coli,”Fizika Zhivogo,4, No. 1, 67–72 (1996).Google Scholar
- 16.S. H. P. Alexander and J. A. Peters,TiPS Receptor & Ion Channel Nomenclature Supplement (1997).Google Scholar
- 17.V. A. Bouryi, A. V. Gourkovskaya and M. F. Shuba, “Identification of transmembrane Ca2+ current of smooth muscle cells in K+-free medium,”Dokl. Akad. Nauk SSSR,268, No. 2, 481–485 (1983).Google Scholar
- 18.V. V. Rekalov, V. M. Taranenko, and M. F. Shuba, “Calcium current in single smooth muscle cells,”Dokl. Akad. Nauk SSSR,276, No. 3, 750–752 (1984).PubMedGoogle Scholar
- 19.V. Ya. Ganitkevich, S. V. Smimov, and M. F. Shuba, “Identification of Ca2+ current in isolated smooth muscle cells,”Dokl. Akad. Nauk SSSR,282, No. 3, 717–720 (1985).PubMedGoogle Scholar
- 20.A. V. Zholos, L. V. Baidan, and M. F. Shuba, “Some properties of Ca2+-induced Ca2+ release mechanism in single visceral smooth muscle cell of the guinea-pig,”J. Physiol.,457, 1–25 (1992).PubMedGoogle Scholar
- 21.A. L. Blatz and K. L. Magleby, “Ion conductance and selectivity of single calcium-activated potassium channels in cultured rat muscle,”J. Gen. Physiol.,84, No. 1, 1–23 (1984).PubMedCrossRefGoogle Scholar
- 22.R. Latorre and C. Miller, “Conduction and selectivity in potassium channels,”J. Membrane Biol.,71, Nos. 1/2, 11–30 (1983).CrossRefGoogle Scholar
- 23.C. D. Benham, T. B. Bolton, R. J. Lang, and T. Takewaki, “The mechanism of action of Ba2+ and TEA on single Ca2+-activated K+ channels in arterial and intestinal smooth muscle cell membranes,”Pflügers Arch.,403, No. 2, 120–127 (1985).PubMedCrossRefGoogle Scholar
- 24.A. Marty, “Ca-dependent K channels with large unitary conductance in chromaffin cell membranes,”Nature,291, 497–500 (1981).PubMedCrossRefGoogle Scholar
- 25.M. Kohler, B. Hirschberg, C. T. Bond, et al., “Small-conductance, calcium-activated potassium channels from mammalian brain,”Science,273, 1709–1714 (1996).PubMedGoogle Scholar
- 26.N. S. Atkinson, G. A. Robertson, and B. Ganetzky, “A component of calcium-activated potassium channels encoded by theDrosophila slo locus,”Science,253, 551–555 (1991).PubMedCrossRefGoogle Scholar
- 27.H. Kolb, “Potassium channels in excitable and non-excitable cells,”Rev. Physiol. Biochem. Pharmacol.,115, 52–91 (1990).Google Scholar
- 28.P. L. Becker, J. J. Singer, J. V. Walsh, and F. S. Fay, “Regulation of calcium concentration in voltage-clamped smooth muscle cells,”Science,244, 211–214 (1989).PubMedCrossRefGoogle Scholar
- 29.V. Ya. Ganitkevich and G. Isenberg, “Depolarization-mediated intracellular calcium transients in isolated smooth muscle cells of guinea-pig urinary bladder,”J. Physiol.,435, 187–205 (1991).Google Scholar
- 30.J. N. Barrett, K. L. Magleby, and B. S. Pallotta, “Properties of single calcium-activated potassium channels in cultured rat muscle,”J. Physiol.,331, 211–230 (1982).PubMedGoogle Scholar
- 31.W. C. Cole and K. M. Sanders, “Characterization of macroscopic outward currents of canine colonic myocytes,”Am. J. Physiol.,26, No. 3, C461-C469 (1989).Google Scholar