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Poster De Conférence Année : 2018

Antinociceptive targets for spider toxins in adult dorsal root ganglia neurons

Résumé

Although necessary for human survival, pain may sometimes become pathologic if long-lasting and associated with alterations in its signaling pathway. Opioid painkillers are officially used to treat moderate to severe, and even mild, pain. However, the consequent strong and not so rare complications that occur, including addiction and overdose, combined with pain management costs, remain an important societal and economic concern. In this context, animal venom toxins represent an original source of peptides for therapeutic treatment to fight against pain and avoid central side effects, and the most appropriate targets seem to be those of neurons located in the dorsal root ganglia (DRG) which convey pain from the skin and tendons to the central nervous system (CNS). Hence, the DRG neurons are well-known to express various families of transmembrane proteins, including ion channels, G-protein-coupled receptors and gap junctions/pannexins. Among the ion channel family, the most studied target for pain treatment is the voltage-gated sodium (NaV) channel subtype NaV1.7. The attraction of scientists for this channel subtype is due to its validation by human genetic diseases as a pain target. Many studies have been reported in the literature to describe gating modulators or pore blockers that affect the functional properties of NaV1.7 channel subtype. The present overview will focus on the fascinating spider venom toxins which represent an original source of proteins possessing complex structures associated with specific electrophysiological effects and prone to be more selective for the NaV1.7 channel subtype mainly expressed in DRG neurons. It will detail (i) the characteristics of these primary sensory neurons, (ii) the electrophysiological properties of the different NaV channel subtypes expressed in these neurons, with a particular attention on the NaV1.7 subtype, and (iii) the features of spider venom toxins, shaped of inhibitory cysteine knot motif, that present high affinity for the NaV1.7 subtype associated with evidenced analgesic efficacy in animal models.
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hal-04467180 , version 1 (20-02-2024)

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  • HAL Id : hal-04467180 , version 1

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Tânia C. Gonçalves, Evelyne Benoit, Michel Partiseti, Denis Servent. Antinociceptive targets for spider toxins in adult dorsal root ganglia neurons. RT25 - 25th Meeting of the French Society of Toxinology – Toxins and Health: From Molecules to Organisms, Nov 2018, Paris, France. . ⟨hal-04467180⟩
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