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Molecular Pharmacology, Vol 19, 345-348, Copyright © 1981 by the American Society for Pharmacology and Experimental Therapeutics
1 Department of Pharmacology, University of Washington, Seattle, Washington 98195, and Division of Environmental
Toxicology and Epidemiology, University of Texas Medical Branch, Galveston, Texas 77550
Ptychodiscus brevis toxin T446 markedly enhances persistent activation of voltage-sensitive sodium channels in neuroblastoma cells by veratridine. Half-maximal enhancement is observed at 50 ng of T446 per milliliter. At maximally effective concentrations, T446 has no effect on specific binding of 125I-labeled scorpion toxin and slightly enhances specific binding of [3H]saxitoxin. Thus, T446 enhances veratridine action but does not bind to any of the three neurotoxin receptor sites on the sodium channels that have been previously described. T446 may act at a new toxin-receptor site associated with voltage-sensitive sodium channels.
Note:
ACKNOWLEDGMENTS
We thank Ms. Cynthia S. Morrow and Ms. Sherryann C. Pesheck
for excellent technical assistance.
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