Characterization of the Electrogenic Sodium Channel from Rat Brain Membranes Using Neurotoxin-Dependent ²²Na Uptake

References

• Albuquerque E. X., Brookes N., Onur R., Warnick J. E. Kinetics of interaction of batrachotoxin and tetrodotoxin on rat diaphragm muscle. Mol. Pharmacol. 1976; 12: 82–91
   Google Scholar
• Albuquerque E. X., Daly J. W. Batrachotoxin, a selective probe for channels modulating sodium conductances in electrogenic membranes. Receptors and Recognition 1 B, P. Curatrecasas. Chapman and Hall, London 1976; 297–338
   Google Scholar
• Albuquerque E. X., McIsaac R. J. Fast and slow mammalian muscles after denervation. Exp. Neurol. 1970; 26: 183–202
   PubMed Web of Science ®Google Scholar
• Albuquerque E. X., Seyama I., Narahashi T. Characterization of batrachotoxin‐induced depolarization of the squid giant axons. J. Pharma. Exp. Ther. 1973; 184: 308–314
   Google Scholar
• Albuquerque E. X., Warnick J. E. The pharmacology of batrachotoxin. IV. Interactions with tetrodotoxin on innervated and chronically denervated rat skeletal muscle. J. Pharmacol. Exp. Ther. 1972; 180: 683–697
   Google Scholar
• Albuquerque E. X., Warnick J. E., Sansone F. M. The pharmacology of batrachotoxin. II. Effect on electrical properties of mammalian nerve and skeletal muscle membranes. J. Pharmacol. Exp. Ther. 1971; 176: 511–528
   PubMed Web of Science ®Google Scholar
• Albuquerque E. X., Warnick J. E., Sansone F. M., Daly J. The pharmacology of batrachotoxin. V. A comparative study of membrane properties and the effect of batrachotoxin on sartorius muscles of the frogs Phyllobates aurotaenia and Rana pipiens. J. Pharmacol. Exp. Ther. 1973; 184: 315–329
   Google Scholar
• Albuquerque E. X., Warnick J. E., Tasse J. R., Sansone F. M. Effects of vinblastine and colchicine on neural regulation of the fast and slow skeletal muscles of the rat. Exp. Neurol. 1972; 37: 607–634
   PubMed Web of Science ®Google Scholar
• Barchi R. L., Weigele J. B. Characteristics of saxitoxin binding to the sodium channel of sarcolemma isolated from rat skeletal muscle. J. Physiol. 1979; 295: 383–396
   Google Scholar
• Blaustein M. P., Goldring J. M. Membrane potentials in pinched off synaptic nerve terminals monitored with a fluorescent probe: Evidence that synaptosomes have potassium diffusion potentials. J. Physiol. (Lond.) 1975; 247: 589–615
   Google Scholar
• Blaustein M. P., Ratzlaff R. W., Kreuger B. K. Uptake of 22Na by presynaptic nerve terminals (synaptosomes): Stimulation by toxins that open sodium channels. Fed. Proc. Abst. 1979; 38: 1198
   Google Scholar
• Bradford H. F., Jones D. G., Ward H. K., Booher J. Biochemical and morphological studies of the short and long term survival of isolated nerve endings. Brain Res. 1975; 90: 245–259
   Google Scholar
• Catterall W. A. Activation of the action potential sodium ionophore of cultured neuroblastoma cells by veratridine and batrachotoxin. J. Biol. Chem. 1975; 250: 4053–4059
   Google Scholar
• Catterall W. A. Membrane potential dependent binding of scorpion toxin to the action potential sodium ionophore. J. Biol. Chem. 1977; 252: 8660–8668
   PubMedGoogle Scholar
• Colquhoun D., Rang H. P., Ritchie J. M. The binding of tetrodo‐toxin and α bungarotoxin to normal and denervated mammalian muscle. J. Physiol. (Lond.) 1974; 240: 199–226
   Google Scholar
• Galper J. B., Catterall W. A. Inhibition of sodium channels by D600. Mol. Pharmacol. 1979; 15: 174–178
   Google Scholar
• Gray E. G., Whittaker P. V. The isolation of nerve endings from brain: An electron‐microscopic study of cell fragments derived by homogenization and centrifugation. J. Anat. (Lond.) 1962; 96: 79–88
   PubMed Web of Science ®Google Scholar
• Grinnel A. D. Phylogenetic gradation of resistance to tetrodotoxin and saxitoxin in puffer fish and related fishes. Procedures First International Conference on Toxic Dinoflagellate Blooms, L. Cicero. Massachusetts Scientific and Technology Foundation, Wakefield, Massachusetts 1975; 377–380
   Google Scholar
• Harris J. B., Marshall M. W. Tetrodotoxin resistant action potentials in newborn rat muscle. Nat. (New Biol.) 1973; 243: 191–192
   Google Scholar
• Harris J. B., Marshall M. W., Ward M. R. Action potential generation in singly and multiply innervated avian muscle fibers. J. Physiol. (Lond.) 1973; 232: 51–52
   Google Scholar
• Harris J. B., Thesleff S. Studies on tetrodotoxin resistant action potentials in denervated skeletal muscle. Acta. Physiol Scand. 1971; 83: 382–388
   Google Scholar
• Henderson R., Strichartz G. Ion fluxes through the sodium channels of garfish olfactory nerve membranes. J. Physiol. (Lond.) 1974; 238: 329–342
   Google Scholar
• Holz R. W., Coyle J. T. The effects of various salts, temperature, and the alkaloids veratridine and batrachotoxin on the uptake of [3H] dopamine into synaptosomes from rat striatum. Mol. Pharmacol. 1974; 10: 746–758
   Google Scholar
• Jacques Y., Fosset M., Lazdunski M. Molecular properties of the action potential Na+ ionophore in neuroblastoma cells. Interactions with neurotoxins. J. Biol. Chem. 1978; 253: 7383–7392
   Google Scholar
• Jansson S. ‐E., Albuquerque E. X., Daly J. The pharmacology of batrachotoxin: VI. Effects on the mammalian motor nerve terminal. J. Pharm. Exp. Ther. 1974; 189: 525–537
   Google Scholar
• Jover E., Martin‐Moutot N., Couraud F., Rochat H. Scorpion toxin: Specific binding to rat synaptosomes. Biochem. Biophys. Res. Commun. 1978; 85: 377–382
   Google Scholar
• Kao C. Y., Furman F. A. Differentiation of the actions of tetrodo‐toxin and saxitoxin. Toxicon 1967; 5: 25–34
   PubMed Web of Science ®Google Scholar
• Khodorov B. I., Peganov E. M., Revenko S. V., Shishkova L. D. Sodium currents in voltage clamped nerve fibers of frog under the combined action of batrachotoxin and procaine. Brain Res. 1975; 84: 541–546
   Google Scholar
• King E. L., Altman C. Schematic method of deriving the rate laws for enzyme‐catalysed reactions. J. Phys. Chem. 1956; 60: 1375–1378
   Web of Science ®Google Scholar
• Lebeda F. J., Warnick J. E., Albuquerque E. X. Electrical and chemosensitive properties of normal and dystrophic chicken muscles. Exp. Neurol. 1974; 43: 21–37
   Google Scholar
• Li P. D., White T. D. Rapid effects of veratridine, tetrodotoxin, gramicidin D, valinomycin and NaCN on the Na+ K+ and ATP contents of synaptosomes. J. Neurochem. 1977; 28: 967–975
   PubMed Web of Science ®Google Scholar
• Matthews J. C., Albuquerque E. X., Eldefrawi M. E. Effects of neurotoxins on the uptake of 22Na by mammalian neural membranes. Fed. Proc. Abst. 1979; 38: 540
   Google Scholar
• Matthews J. C., Albuquerque E. X., Eldefrawi M. E. Influence of batrachotoxin, veratridine, grayanotoxin I and tetrodotoxin on uptake of Na‐22 by brain membrane preparations. Life Sci. 1979; 25: 1651–1658
   Google Scholar
• Narahashi T. Restoration of action potential by anodal polarization in lobster giant axons. J. Cell Comp. Physiol. 1964; 64: 73–96
   Google Scholar
• Narahashi T. Chemicals as tools in the study of excitable membranes. Physiol. Rev. 1974; 54: 813–889
   PubMed Web of Science ®Google Scholar
• Radharaman R., Morrow C. S., Catterall W. A. Binding of scorpion toxin to receptor sites associated with voltage sensitive sodium channels in synaptic nerve ending particles. J. Biol. Chem. 1978; 253: 7307–7313
   Google Scholar
• Redfern P., Thesleff S. Action potential generation in denervated rat skeletal muscle. II. The action of tetrodotoxin. Acta Physiol. Scand. 1971; 82: 70–78
   Google Scholar
• Ritchie J. M., Rogart R. B. The binding of saxitoxin and tetrodotoxin to excitable tissue. Rev. Physiol. Biochem. Pharmacol. 1977; 79: 1–50
   PubMed Web of Science ®Google Scholar
• Villegas R., Villegas G. M., Barnoia F. V., Racker E. Incorporation of the sodium channel of lobster nerve into artificial liposomes. Biochem. Biophys. Res. Commun. 1977; 79: 210–217
   Google Scholar
• Weigele J. B., Barchi R. L. Saxitoxin binding to the mammalian sodium channel. Competition by monovalent and divalent cations. FEBS Letters 1978; 95: 49–53
   Google Scholar