Front. Pharmacol. Frontiers in Pharmacology Front. Pharmacol. 1663-9812 Frontiers Media S.A. 10.3389/fphar.2018.01241 Pharmacology Correction Corrigendum: The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons Gonçalves Tânia C. 1 2 Benoit Evelyne 2 3 Partiseti Michel 1 Servent Denis 2 * 1Sanofi R&D, Integrated Drug Discovery – High Content Biology, Paris, France 2Service d'Ingénierie Moléculaire des Protéines, CEA de Saclay, Université Paris-Saclay, Gif-sur-Yvette, France 3Institut des Neurosciences Paris-Saclay, UMR CNRS/Université Paris-Sud 9197, Gif-sur-Yvette, France

Edited and reviewed by: Yuri N. Utkin, Institute of Bioorganic Chemistry (RAS), Russia

 *Correspondence: Denis Servent denis.servent@cea.fr

This article was submitted to Pharmacology of Ion Channels and Channelopathies, a section of the journal Frontiers in Pharmacology

 24 10 2018 2018 9 1241 05 10 2018 12 10 2018 Copyright © 2018 Gonçalves, Benoit, Partiseti and Servent. 2018 Gonçalves, Benoit, Partiseti and Servent

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 A Corrigendum on The NaV1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons by Gonçalves, T. C., Benoit, E., Partiseti, M., and Servent, D. (2018) Front. Pharmacol. 9:1000. doi: 10.3389/fphar.2018.01000 voltage-gated sodium channels NaV1.7 channel subtype spider toxins pain dorsal root ganglia neurons electrophysiology

In the original article, there was a mistake in Figure 1 as published. Nociceptors (C-fibers) and Proprioceptors (Aδ-fibers) instead of Nociceptors (Aδ/C fibers) and Proprioceptors (Aα fibers). The corrected Figure 1 appears below. The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Cellular elements involved in pain transmission from the peripheral to the central nervous system (CNS). (Box 1) The pain (thermal, high pressure, mechanical, chemical) information is first detected by the receptors located at the level of free nerve endings of primary sensory neuron (PSN) fibers. (Box 2) Then, it is conveyed by the dendrites of these neurons, components of dorsal root ganglia (DRG), to the dorsal horn of spinal cord where it is transmitted to the dendrites of secondary sensory neurons (SSNs). (Box 3) Finally, it is brought to the hypothalamus via the tertiary sensory neurons (TSNs) whose cell bodies constitute, in part, the brain cortex.

 Conflict of interest statement

TG and MP are current or former employees of Sanofi. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.