Dual action of a dinoflagellate-derived precursor of Pacific ciguatoxins (P-CTX-4B) on voltage-dependent K and Na channels of single myelinated axons |
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Authors: | Sé bastien Schlumberger,Jordi Molgó |
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Affiliation: | CNRS, Institut de Neurobiologie Alfred Fessard - FRC2118, Laboratoire de Neurobiologie Cellulaire et Moléculaire - UPR9040, 91198 Gif sur Yvette cedex, France |
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Abstract: | The effects of Pacific ciguatoxin-4B (P-CTX-4B, also named gambiertoxin), extracted from toxic Gambierdiscus dinoflagellates, were assessed on nodal K+ and Na+ currents of frog myelinated axons, using a conventional voltage-clamp technique. P-CTX-4B decreased, within a few minutes, both K+ and Na+ currents in a dose-dependent manner, without inducing any marked change in current kinetics. The toxin was more effective in blocking K+ than Na+ channels. P-CTX-4B shifted the voltage-dependence of Na+ conductance by about 14 mV towards more negative membrane potentials. This effect was reversed by increasing Ca2+ in the external solution. A negative shift of about 16 mV in the steady-state Na+ inactivation-voltage curve was also observed in the presence of the toxin. Unmodified and P-CTX-4B-modified Na+ currents were similarly affected by the local anaesthetic lidocaine. The decrease of the two currents by lidocaine was dependent on both the concentration and the membrane potential during pre-pulses. In conclusion, P-CTX-4B appears about four times more effective than P-CTX-1B to affect K+ channels, whereas it is about 50 times less efficient to affect Na+ channels of axonal membranes. These actions may be related to subtle differences between the two chemical structures of molecules. |
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Keywords: | Gambiertoxin Gambierdiscus toxicus dinoflagellate Ciguatoxin K+ channels Na+ channels Myelinated axons |
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