Cargando…

Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics

Sensation and action are necessarily coupled during stimulus perception – while tasting, for instance, perception happens while an animal decides to expel or swallow the substance in the mouth (the former via a behavior known as ‘gaping’). Taste responses in the rodent gustatory cortex (GC) span thi...

Descripción completa

Detalles Bibliográficos
Autores principales: Mukherjee, Narendra, Wachutka, Joseph, Katz, Donald B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625792/
https://www.ncbi.nlm.nih.gov/pubmed/31232693
http://dx.doi.org/10.7554/eLife.45968
_version_ 1783434467943120896
author Mukherjee, Narendra
Wachutka, Joseph
Katz, Donald B
author_facet Mukherjee, Narendra
Wachutka, Joseph
Katz, Donald B
author_sort Mukherjee, Narendra
collection PubMed
description Sensation and action are necessarily coupled during stimulus perception – while tasting, for instance, perception happens while an animal decides to expel or swallow the substance in the mouth (the former via a behavior known as ‘gaping’). Taste responses in the rodent gustatory cortex (GC) span this sensorimotor divide, progressing through firing-rate epochs that culminate in the emergence of action-related firing. Population analyses reveal this emergence to be a sudden, coherent and variably-timed ensemble transition that reliably precedes gaping onset by 0.2–0.3s. Here, we tested whether this transition drives gaping, by delivering 0.5s GC perturbations in tasting trials. Perturbations significantly delayed gaping, but only when they preceded the action-related transition - thus, the same perturbation impacted behavior or not, depending on the transition latency in that particular trial. Our results suggest a distributed attractor network model of taste processing, and a dynamical role for cortex in driving motor behavior.
format Online
Article
Text
id pubmed-6625792
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-66257922019-07-15 Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics Mukherjee, Narendra Wachutka, Joseph Katz, Donald B eLife Neuroscience Sensation and action are necessarily coupled during stimulus perception – while tasting, for instance, perception happens while an animal decides to expel or swallow the substance in the mouth (the former via a behavior known as ‘gaping’). Taste responses in the rodent gustatory cortex (GC) span this sensorimotor divide, progressing through firing-rate epochs that culminate in the emergence of action-related firing. Population analyses reveal this emergence to be a sudden, coherent and variably-timed ensemble transition that reliably precedes gaping onset by 0.2–0.3s. Here, we tested whether this transition drives gaping, by delivering 0.5s GC perturbations in tasting trials. Perturbations significantly delayed gaping, but only when they preceded the action-related transition - thus, the same perturbation impacted behavior or not, depending on the transition latency in that particular trial. Our results suggest a distributed attractor network model of taste processing, and a dynamical role for cortex in driving motor behavior. eLife Sciences Publications, Ltd 2019-06-24 /pmc/articles/PMC6625792/ /pubmed/31232693 http://dx.doi.org/10.7554/eLife.45968 Text en © 2019, Mukherjee et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mukherjee, Narendra
Wachutka, Joseph
Katz, Donald B
Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title_full Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title_fullStr Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title_full_unstemmed Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title_short Impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
title_sort impact of precisely-timed inhibition of gustatory cortex on taste behavior depends on single-trial ensemble dynamics
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625792/
https://www.ncbi.nlm.nih.gov/pubmed/31232693
http://dx.doi.org/10.7554/eLife.45968
work_keys_str_mv AT mukherjeenarendra impactofpreciselytimedinhibitionofgustatorycortexontastebehaviordependsonsingletrialensembledynamics
AT wachutkajoseph impactofpreciselytimedinhibitionofgustatorycortexontastebehaviordependsonsingletrialensembledynamics
AT katzdonaldb impactofpreciselytimedinhibitionofgustatorycortexontastebehaviordependsonsingletrialensembledynamics