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Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons

Adaptation plays an important role in sensory systems as it dynamically modifies sensitivity to allow the detection of stimulus changes. The vomeronasal system controls many social behaviors in most mammals by detecting pheromones released by conspecifics. Stimuli activate a transduction cascade in...

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Autores principales: Sarno, Nicole, Hernandez-Clavijo, Andres, Boccaccio, Anna, Menini, Anna, Pifferi, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116931/
https://www.ncbi.nlm.nih.gov/pubmed/35487703
http://dx.doi.org/10.1523/ENEURO.0471-21.2022
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author Sarno, Nicole
Hernandez-Clavijo, Andres
Boccaccio, Anna
Menini, Anna
Pifferi, Simone
author_facet Sarno, Nicole
Hernandez-Clavijo, Andres
Boccaccio, Anna
Menini, Anna
Pifferi, Simone
author_sort Sarno, Nicole
collection PubMed
description Adaptation plays an important role in sensory systems as it dynamically modifies sensitivity to allow the detection of stimulus changes. The vomeronasal system controls many social behaviors in most mammals by detecting pheromones released by conspecifics. Stimuli activate a transduction cascade in vomeronasal neurons that leads to spiking activity. Whether and how these neurons adapt to stimuli is still debated and largely unknown. Here, we measured short-term adaptation performing current-clamp whole-cell recordings by using diluted urine as a stimulus, as it contains many pheromones. We measured spike frequency adaptation in response to repeated identical stimuli of 2–10 s duration that was dependent on the time interval between stimuli. Responses to paired current steps, bypassing the signal transduction cascade, also showed spike frequency adaptation. We found that voltage-gated Na(+) channels in VSNs undergo slow inactivation processes. Furthermore, recovery from slow inactivation of voltage-gated Na(+) channels occurs in several seconds, a time scale similar to that measured during paired-pulse adaptation protocols, suggesting that it partially contributes to short-term spike frequency adaptation. We conclude that vomeronasal neurons do exhibit a time-dependent short-term spike frequency adaptation to repeated natural stimuli and that slow inactivation of Na(+) channels contributes to this form of adaptation. These findings not only increase our knowledge about adaptation in the vomeronasal system, but also raise the question of whether slow inactivation of Na(+) channels may play a role in other sensory systems.
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spelling pubmed-91169312022-05-19 Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons Sarno, Nicole Hernandez-Clavijo, Andres Boccaccio, Anna Menini, Anna Pifferi, Simone eNeuro Research Article: New Research Adaptation plays an important role in sensory systems as it dynamically modifies sensitivity to allow the detection of stimulus changes. The vomeronasal system controls many social behaviors in most mammals by detecting pheromones released by conspecifics. Stimuli activate a transduction cascade in vomeronasal neurons that leads to spiking activity. Whether and how these neurons adapt to stimuli is still debated and largely unknown. Here, we measured short-term adaptation performing current-clamp whole-cell recordings by using diluted urine as a stimulus, as it contains many pheromones. We measured spike frequency adaptation in response to repeated identical stimuli of 2–10 s duration that was dependent on the time interval between stimuli. Responses to paired current steps, bypassing the signal transduction cascade, also showed spike frequency adaptation. We found that voltage-gated Na(+) channels in VSNs undergo slow inactivation processes. Furthermore, recovery from slow inactivation of voltage-gated Na(+) channels occurs in several seconds, a time scale similar to that measured during paired-pulse adaptation protocols, suggesting that it partially contributes to short-term spike frequency adaptation. We conclude that vomeronasal neurons do exhibit a time-dependent short-term spike frequency adaptation to repeated natural stimuli and that slow inactivation of Na(+) channels contributes to this form of adaptation. These findings not only increase our knowledge about adaptation in the vomeronasal system, but also raise the question of whether slow inactivation of Na(+) channels may play a role in other sensory systems. Society for Neuroscience 2022-05-13 /pmc/articles/PMC9116931/ /pubmed/35487703 http://dx.doi.org/10.1523/ENEURO.0471-21.2022 Text en Copyright © 2022 Sarno et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Sarno, Nicole
Hernandez-Clavijo, Andres
Boccaccio, Anna
Menini, Anna
Pifferi, Simone
Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title_full Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title_fullStr Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title_full_unstemmed Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title_short Slow Inactivation of Sodium Channels Contributes to Short-Term Adaptation in Vomeronasal Sensory Neurons
title_sort slow inactivation of sodium channels contributes to short-term adaptation in vomeronasal sensory neurons
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116931/
https://www.ncbi.nlm.nih.gov/pubmed/35487703
http://dx.doi.org/10.1523/ENEURO.0471-21.2022
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