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A new conotoxin isolated from Conus consors venom acting selectively on axons and motor nerve terminals through a Na+-dependent mechanism

Authors :
Le Gall, Frédéric
Favreau, Philippe
Benoit, Evelyne
Mattei, César
Bouet, Françoise
Menou, Jean-Louis
Ménez, André
Letourneux, Yves
Molgó, Jordi
Département d'Ingénierie et d'Etudes des Protéines
CEN/Saclay
Laboratoire de neurobiologie cellulaire et moléculaire (NBCM)
Centre National de la Recherche Scientifique (CNRS)
Service d'anatomie et cytologie pathologiques [Rennes]
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes]
Institut de Recherche pour le Développement (IRD)
Muséum national d'Histoire naturelle (MNHN)
Laboratoire des Substances Naturelles
Service d'anatomie et cytologie pathologiques [Rennes] = Anatomy and Cytopathology [Rennes]
CHU Pontchaillou [Rennes]
Source :
European Journal of Neuroscience, European Journal of Neuroscience, Wiley, 1999, 11 (9), pp.3134-3142. ⟨10.1046/j.1460-9568.1999.00732.x⟩
Publication Year :
1999

Abstract

International audience; A novel conotoxin was isolated and characterized from the venom of the fish-hunting marine snail Conus consors. The peptide was identified by screening chromatography fractions of the crude venom that produced a marked contraction and extension of the caudal and dorsal fins in fish, and noticeable spontaneous contractions of isolated frog neuromuscular preparations. The peptide, named CcTX, had 30 amino acids and the following scaffold: X11CCX7CX2CXCX3C. At the frog neuromuscular junction, CcTx at nanomolar concentrations selectively increased nerve terminal excitability so that a single nerve stimulation triggered trains of repetitive or spontaneous synaptic potentials and action potentials. In contrast, CcTx had no noticeable effect on muscle excitability even at concentrations 100 x higher than those that affected motor nerve terminals, as revealed by direct muscle stimulation. In addition, CcTx increased miniature endplate potential (MEPP) frequency in a Ca2+-free medium supplemented with ethylene glycol-bis-(beta-aminoethyl ether)-N,N,N', N'-tetraacetic acid (EGTA). Blockade of voltage-dependent sodium channels with tetrodotoxin (TTX) either prevented or suppressed the increase of MEPP frequency induced by the toxin. CcTx also produced a TTX-sensitive depolarization of the nodal membrane in single myelinated axons giving rise, in some cases, to repetitive and/or spontaneous action potential discharges. In addition, CcTx increased the nodal volume of myelinated axons, as determined using confocal laser scanning microscopy. This increase was reversed by external hyperosmolar solutions and was prevented by pretreatment of axons with TTX. It is suggested that CcTx, by specifically activating neuronal voltage-gated sodium channels at the resting membrane potential, produced Na+ entry into nerve terminals and axons without directly affecting skeletal muscle fibres. CcTx belongs to a novel family of conotoxins that targets neuronal voltage-gated sodium channels.

Details

ISSN :
0953816X and 14609568
Volume :
11
Issue :
9
Database :
OpenAIRE
Journal :
The European journal of neuroscience
Accession number :
edsair.pmid.dedup....b97bd62e3923aa0716e279ff4196c42c
Full Text :
https://doi.org/10.1046/j.1460-9568.1999.00732.x⟩