Cargando…
Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit
Behavioral variability is thought to be critical for trial and error learning, but where such motor exploration is generated in the central nervous system is unclear. The zebra finch songbird species offers a highly appropriate model in which to address this question. The male song is amenable to de...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913712/ https://www.ncbi.nlm.nih.gov/pubmed/29687960 http://dx.doi.org/10.14814/phy2.13638 |
_version_ | 1783316591262302208 |
---|---|
author | Heston, Jonathan B. Simon, Joseph Day, Nancy F. Coleman, Melissa J. White, Stephanie A. |
author_facet | Heston, Jonathan B. Simon, Joseph Day, Nancy F. Coleman, Melissa J. White, Stephanie A. |
author_sort | Heston, Jonathan B. |
collection | PubMed |
description | Behavioral variability is thought to be critical for trial and error learning, but where such motor exploration is generated in the central nervous system is unclear. The zebra finch songbird species offers a highly appropriate model in which to address this question. The male song is amenable to detailed measurements of variability, while the brain contains an identified cortico‐basal ganglia loop that underlies this behavior. We used pharmacogenetic interventions to separately interrogate cortical and basal ganglia nodes of zebra finch song control circuitry. We show that bidirectional manipulations of each node produce near mirror image changes in vocal control: Cortical activity promotes song variability, whereas basal ganglia activity promotes song stability. Furthermore, female conspecifics can detect these pharmacogenetically elicited changes in song quality. Our results indicate that cortex and striatopallidum can jointly and reciprocally affect behaviorally relevant levels of vocal variability, and point to endogenous mechanisms for its control. |
format | Online Article Text |
id | pubmed-5913712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59137122018-04-30 Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit Heston, Jonathan B. Simon, Joseph Day, Nancy F. Coleman, Melissa J. White, Stephanie A. Physiol Rep Original Research Behavioral variability is thought to be critical for trial and error learning, but where such motor exploration is generated in the central nervous system is unclear. The zebra finch songbird species offers a highly appropriate model in which to address this question. The male song is amenable to detailed measurements of variability, while the brain contains an identified cortico‐basal ganglia loop that underlies this behavior. We used pharmacogenetic interventions to separately interrogate cortical and basal ganglia nodes of zebra finch song control circuitry. We show that bidirectional manipulations of each node produce near mirror image changes in vocal control: Cortical activity promotes song variability, whereas basal ganglia activity promotes song stability. Furthermore, female conspecifics can detect these pharmacogenetically elicited changes in song quality. Our results indicate that cortex and striatopallidum can jointly and reciprocally affect behaviorally relevant levels of vocal variability, and point to endogenous mechanisms for its control. John Wiley and Sons Inc. 2018-04-24 /pmc/articles/PMC5913712/ /pubmed/29687960 http://dx.doi.org/10.14814/phy2.13638 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Heston, Jonathan B. Simon, Joseph Day, Nancy F. Coleman, Melissa J. White, Stephanie A. Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title | Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title_full | Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title_fullStr | Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title_full_unstemmed | Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title_short | Bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
title_sort | bidirectional scaling of vocal variability by an avian cortico‐basal ganglia circuit |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913712/ https://www.ncbi.nlm.nih.gov/pubmed/29687960 http://dx.doi.org/10.14814/phy2.13638 |
work_keys_str_mv | AT hestonjonathanb bidirectionalscalingofvocalvariabilitybyanaviancorticobasalgangliacircuit AT simonjoseph bidirectionalscalingofvocalvariabilitybyanaviancorticobasalgangliacircuit AT daynancyf bidirectionalscalingofvocalvariabilitybyanaviancorticobasalgangliacircuit AT colemanmelissaj bidirectionalscalingofvocalvariabilitybyanaviancorticobasalgangliacircuit AT whitestephaniea bidirectionalscalingofvocalvariabilitybyanaviancorticobasalgangliacircuit |