Abstract
1. External Ca2+ block of Na+ channels was studied by a gigaohm-seal patch clamp technique in single cardiac ventricular cells from guinea-pig. Single-channel currents were recorded from cell-attached patches. 2. Increasing external Ca2+ concentrations in the patch pipette from 0.1 to 20 mM reduced the single-channel conductance of normal Na+ channels from 27 to 14 pS without causing flickering (obtained from linear regression, eight patches). 3. Exposed to external Ca2+ concentrations of 20 mM, the single-channel currents decreased at potentials negative to -60 mV in spite of an increased driving force for inward Na+ currents. 4. An external concentration of 35 mM-Mg2+, which is supposed to exert a screening of surface charges nearly equal to that of 20 mM-Ca2+ (Hille, Woodhull & Shapiro, 1975), reduced the single-Na+-channel conductance only from 26 (1 mM-Mg2+) to 20 pS (linear regression, eight patches). A weaker voltage-dependent block at potentials negative to -50 mV was observed in 35 mM-Mg2+ than in 20 mM-Ca2+. Therefore, surface charge effects cannot explain the obvious reduction of the conductance of single Na+ channels found when the external Ca2+ concentration was increased. 5. Single Na+-channel currents increased with an increase in the external Na+ concentration [( Na+]o) but showed saturation. The Na+o-single-channel current relationship could be described by i = imax/(1 + kd/[Na+]o) with imax = 5.4 pA and kd = 359 mM (seventeen patches). 6. The mean open time of Na+ channels varied between 0.18 and 0.59 ms (potentials between -80 and -20 mV). No significant changes in the mean open time could be obtained when Ca2+ was varied between 0.1 and 20 mM. 7. The piperazinylindole compound DPI 201-106 was used as a tool to prolong the open time of single Na+ channels. If the external Ca2+ concentration was increased from 0.1 to 20 mM the currents through the modified channels were reduced. The reduction of single-channel currents was accentuated at potentials negative to -60 mV (20 mM-Ca2+) similar to the control channels. 8. In contrast to non-modified Na+ channels, the mean open time of DPI 201-106-modified channels proved extremely voltage and Ca2+ dependent.(ABSTRACT TRUNCATED AT 400 WORDS)
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Selected References
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- Baer M., Best P. M., Reuter H. Voltage-dependent action of tetrodotoxin in mammalian cardiac muscle. Nature. 1976 Sep 23;263(5575):344–345. doi: 10.1038/263344a0. [DOI] [PubMed] [Google Scholar]
- Benndorf K., Boldt W., Nilius B. Sodium current in single myocardial mouse cells. Pflugers Arch. 1985 May;404(2):190–196. doi: 10.1007/BF00585418. [DOI] [PubMed] [Google Scholar]
- Cachelin A. B., De Peyer J. E., Kokubun S., Reuter H. Sodium channels in cultured cardiac cells. J Physiol. 1983 Jul;340:389–401. doi: 10.1113/jphysiol.1983.sp014768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carmeliet E. Voltage-dependent block by tetrodotoxin of the sodium channel in rabbit cardiac Purkinje fibers. Biophys J. 1987 Jan;51(1):109–114. doi: 10.1016/S0006-3495(87)83315-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen C. J., Bean B. P., Colatsky T. J., Tsien R. W. Tetrodotoxin block of sodium channels in rabbit Purkinje fibers. Interactions between toxin binding and channel gating. J Gen Physiol. 1981 Oct;78(4):383–411. doi: 10.1085/jgp.78.4.383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coronado R., Affolter H. Insulation of the conduction pathway of muscle transverse tubule calcium channels from the surface charge of bilayer phospholipid. J Gen Physiol. 1986 Jun;87(6):933–953. doi: 10.1085/jgp.87.6.933. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fozzard H. A., January C. T., Makielski J. C. New studies of the excitatory sodium currents in heart muscle. Circ Res. 1985 Apr;56(4):475–485. doi: 10.1161/01.res.56.4.475. [DOI] [PubMed] [Google Scholar]
- Grant A. O., Starmer C. F., Strauss H. C. Unitary sodium channels in isolated cardiac myocytes of rabbit. Circ Res. 1983 Dec;53(6):823–829. doi: 10.1161/01.res.53.6.823. [DOI] [PubMed] [Google Scholar]
- 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]
- Hess P., Lansman J. B., Tsien R. W. Calcium channel selectivity for divalent and monovalent cations. Voltage and concentration dependence of single channel current in ventricular heart cells. J Gen Physiol. 1986 Sep;88(3):293–319. doi: 10.1085/jgp.88.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hille B. Ionic selectivity, saturation, and block in sodium channels. A four-barrier model. J Gen Physiol. 1975 Nov;66(5):535–560. doi: 10.1085/jgp.66.5.535. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hille B., Woodhull A. M., Shapiro B. I. Negative surface charge near sodium channels of nerve: divalent ions, monovalent ions, and pH. Philos Trans R Soc Lond B Biol Sci. 1975 Jun 10;270(908):301–318. doi: 10.1098/rstb.1975.0011. [DOI] [PubMed] [Google Scholar]
- Kao R. L., Christman E. W., Luh S. L., Krauhs J. M., Tyers G. F., Williams E. H. The effects of insulin and anoxia on the metabolism of isolated mature rat cardiac myocytes. Arch Biochem Biophys. 1980 Sep;203(2):587–599. doi: 10.1016/0003-9861(80)90216-7. [DOI] [PubMed] [Google Scholar]
- Kohlhardt M., Fröbe U., Herzig J. W. Modification of single cardiac Na+ channels by DPI 201-106. J Membr Biol. 1986;89(2):163–172. doi: 10.1007/BF01869712. [DOI] [PubMed] [Google Scholar]
- Krueger B. K., Worley J. F., 3rd, French R. J. Single sodium channels from rat brain incorporated into planar lipid bilayer membranes. Nature. 1983 May 12;303(5913):172–175. doi: 10.1038/303172a0. [DOI] [PubMed] [Google Scholar]
- Kunze D. L., Lacerda A. E., Wilson D. L., Brown A. M. Cardiac Na currents and the inactivating, reopening, and waiting properties of single cardiac Na channels. J Gen Physiol. 1985 Nov;86(5):691–719. doi: 10.1085/jgp.86.5.691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lansman J. B., Hess P., Tsien R. W. Blockade of current through single calcium channels by Cd2+, Mg2+, and Ca2+. Voltage and concentration dependence of calcium entry into the pore. J Gen Physiol. 1986 Sep;88(3):321–347. doi: 10.1085/jgp.88.3.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mozhayeva G. N., Naumov A. P., Nosyreva E. D. Potential-dependent calcium blockage of normal and aconitine-modified sodium channels in frog node of Ranvier. Gen Physiol Biophys. 1985 Aug;4(4):425–427. [PubMed] [Google Scholar]
- Nilius B., Benndorf K., Markwardt F. Effects of lidocaine on single cardiac sodium channels. J Mol Cell Cardiol. 1987 Sep;19(9):865–874. doi: 10.1016/s0022-2828(87)80615-6. [DOI] [PubMed] [Google Scholar]
- Nilius B., Benndorf K., Markwardt F. Modified gating behaviour of aconitine treated single sodium channels from adult cardiac myocytes. Pflugers Arch. 1986 Dec;407(6):691–693. doi: 10.1007/BF00582653. [DOI] [PubMed] [Google Scholar]
- Nilius B., Marinov B. S. Current-dependent gating of single cardiac sodium channels? Gen Physiol Biophys. 1987 Dec;6(6):655–658. [PubMed] [Google Scholar]
- Patlak J. B., Ortiz M. Slow currents through single sodium channels of the adult rat heart. J Gen Physiol. 1985 Jul;86(1):89–104. doi: 10.1085/jgp.86.1.89. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sheets M. F., Scanley B. E., Hanck D. A., Makielski J. C., Fozzard H. A. Open sodium channel properties of single canine cardiac Purkinje cells. Biophys J. 1987 Jul;52(1):13–22. doi: 10.1016/S0006-3495(87)83183-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stimers J. R., Bezanilla F., Taylor R. E. Sodium channel activation in the squid giant axon. Steady state properties. J Gen Physiol. 1985 Jan;85(1):65–82. doi: 10.1085/jgp.85.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vassilev P. M., Hadley R. W., Lee K. S., Hume J. R. Voltage-dependent action of tetrodotoxin in mammalian cardiac myocytes. Am J Physiol. 1986 Aug;251(2 Pt 2):H475–H480. doi: 10.1152/ajpheart.1986.251.2.H475. [DOI] [PubMed] [Google Scholar]
- Woodhull A. M. Ionic blockage of sodium channels in nerve. J Gen Physiol. 1973 Jun;61(6):687–708. doi: 10.1085/jgp.61.6.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Worley J. F., 3rd, French R. J., Krueger B. K. Trimethyloxonium modification of single batrachotoxin-activated sodium channels in planar bilayers. Changes in unit conductance and in block by saxitoxin and calcium. J Gen Physiol. 1986 Feb;87(2):327–349. doi: 10.1085/jgp.87.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamamoto D., Yeh J. Z., Narahashi T. Interactions of permeant cations with sodium channels of squid axon membranes. Biophys J. 1985 Sep;48(3):361–368. doi: 10.1016/S0006-3495(85)83792-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamamoto D., Yeh J. Z., Narahashi T. Voltage-dependent calcium block of normal and tetramethrin-modified single sodium channels. Biophys J. 1984 Jan;45(1):337–344. doi: 10.1016/S0006-3495(84)84159-4. [DOI] [PMC free article] [PubMed] [Google Scholar]