Cargando…
Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets
Animals have evolved specialized neural circuits to defend themselves from pain- and injury-causing stimuli. Using a combination of optical, behavioral and genetic approaches in the larval zebrafish, we describe a novel role for hypothalamic oxytocin (OXT) neurons in the processing of noxious stimul...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820349/ https://www.ncbi.nlm.nih.gov/pubmed/31358991 http://dx.doi.org/10.1038/s41593-019-0452-x |
_version_ | 1783463919754412032 |
---|---|
author | Wee, Caroline L. Nikitchenko, Maxim Wang, Wei-Chun Luks-Morgan, Sasha Song, Erin Gagnon, James Randlett, Owen Bianco, Isaac H. Lacoste, Alix M. B. Glushenkova, Elena Barrios, Joshua P. Schier, Alexander F. Kunes, Samuel Engert, Florian Douglass, Adam D. |
author_facet | Wee, Caroline L. Nikitchenko, Maxim Wang, Wei-Chun Luks-Morgan, Sasha Song, Erin Gagnon, James Randlett, Owen Bianco, Isaac H. Lacoste, Alix M. B. Glushenkova, Elena Barrios, Joshua P. Schier, Alexander F. Kunes, Samuel Engert, Florian Douglass, Adam D. |
author_sort | Wee, Caroline L. |
collection | PubMed |
description | Animals have evolved specialized neural circuits to defend themselves from pain- and injury-causing stimuli. Using a combination of optical, behavioral and genetic approaches in the larval zebrafish, we describe a novel role for hypothalamic oxytocin (OXT) neurons in the processing of noxious stimuli. In vivo imaging reveals that a large and distributed fraction of zebrafish OXT neurons responds strongly to noxious inputs, including the activation of damage-sensing TRPA1 receptors. OXT population activity reflects the sensorimotor transformation of the noxious stimulus, with some neurons encoding sensory information and others correlating more strongly with large-angle swims. Notably, OXT neuron activation is sufficient to generate this defensive behavior via the recruitment of brainstem premotor targets, whereas ablation of OXT neurons or loss of the peptide attenuate behavioral responses to TRPA1 activation. These data highlight a crucial role for OXT neurons in the generation of appropriate defensive responses to noxious input. |
format | Online Article Text |
id | pubmed-6820349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-68203492020-01-29 Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets Wee, Caroline L. Nikitchenko, Maxim Wang, Wei-Chun Luks-Morgan, Sasha Song, Erin Gagnon, James Randlett, Owen Bianco, Isaac H. Lacoste, Alix M. B. Glushenkova, Elena Barrios, Joshua P. Schier, Alexander F. Kunes, Samuel Engert, Florian Douglass, Adam D. Nat Neurosci Article Animals have evolved specialized neural circuits to defend themselves from pain- and injury-causing stimuli. Using a combination of optical, behavioral and genetic approaches in the larval zebrafish, we describe a novel role for hypothalamic oxytocin (OXT) neurons in the processing of noxious stimuli. In vivo imaging reveals that a large and distributed fraction of zebrafish OXT neurons responds strongly to noxious inputs, including the activation of damage-sensing TRPA1 receptors. OXT population activity reflects the sensorimotor transformation of the noxious stimulus, with some neurons encoding sensory information and others correlating more strongly with large-angle swims. Notably, OXT neuron activation is sufficient to generate this defensive behavior via the recruitment of brainstem premotor targets, whereas ablation of OXT neurons or loss of the peptide attenuate behavioral responses to TRPA1 activation. These data highlight a crucial role for OXT neurons in the generation of appropriate defensive responses to noxious input. 2019-07-29 2019-09 /pmc/articles/PMC6820349/ /pubmed/31358991 http://dx.doi.org/10.1038/s41593-019-0452-x Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wee, Caroline L. Nikitchenko, Maxim Wang, Wei-Chun Luks-Morgan, Sasha Song, Erin Gagnon, James Randlett, Owen Bianco, Isaac H. Lacoste, Alix M. B. Glushenkova, Elena Barrios, Joshua P. Schier, Alexander F. Kunes, Samuel Engert, Florian Douglass, Adam D. Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title | Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title_full | Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title_fullStr | Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title_full_unstemmed | Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title_short | Zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
title_sort | zebrafish oxytocin neurons drive nocifensive behavior via brainstem premotor targets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820349/ https://www.ncbi.nlm.nih.gov/pubmed/31358991 http://dx.doi.org/10.1038/s41593-019-0452-x |
work_keys_str_mv | AT weecarolinel zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT nikitchenkomaxim zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT wangweichun zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT luksmorgansasha zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT songerin zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT gagnonjames zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT randlettowen zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT biancoisaach zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT lacostealixmb zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT glushenkovaelena zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT barriosjoshuap zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT schieralexanderf zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT kunessamuel zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT engertflorian zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets AT douglassadamd zebrafishoxytocinneuronsdrivenocifensivebehaviorviabrainstempremotortargets |