Cargando…

Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice

To survive in an ever-changing environment, animals must detect and learn salient information. The anterior insular cortex (aIC) and medial prefrontal cortex (mPFC) are heavily implicated in salience and novelty processing, and specifically, the processing of taste sensory information. Here, we exam...

Descripción completa

Detalles Bibliográficos
Autores principales: Kayyal, Haneen, Chandran, Sailendrakumar Kolatt, Yiannakas, Adonis, Gould, Nathaniel, Khamaisy, Mohammad, Rosenblum, Kobi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282338/
https://www.ncbi.nlm.nih.gov/pubmed/34219650
http://dx.doi.org/10.7554/eLife.66686
_version_ 1783722990550122496
author Kayyal, Haneen
Chandran, Sailendrakumar Kolatt
Yiannakas, Adonis
Gould, Nathaniel
Khamaisy, Mohammad
Rosenblum, Kobi
author_facet Kayyal, Haneen
Chandran, Sailendrakumar Kolatt
Yiannakas, Adonis
Gould, Nathaniel
Khamaisy, Mohammad
Rosenblum, Kobi
author_sort Kayyal, Haneen
collection PubMed
description To survive in an ever-changing environment, animals must detect and learn salient information. The anterior insular cortex (aIC) and medial prefrontal cortex (mPFC) are heavily implicated in salience and novelty processing, and specifically, the processing of taste sensory information. Here, we examined the role of aIC-mPFC reciprocal connectivity in novel taste neophobia and memory formation, in mice. Using pERK and neuronal intrinsic properties as markers for neuronal activation, and retrograde AAV (rAAV) constructs for connectivity, we demonstrate a correlation between aIC-mPFC activity and novel taste experience. Furthermore, by expressing inhibitory chemogenetic receptors in these projections, we show that aIC-to-mPFC activity is necessary for both taste neophobia and its attenuation. However, activity within mPFC-to-aIC projections is essential only for the neophobic reaction but not for the learning process. These results provide an insight into the cortical circuitry needed to detect, react to- and learn salient stimuli, a process critically involved in psychiatric disorders.
format Online
Article
Text
id pubmed-8282338
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-82823382021-07-19 Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice Kayyal, Haneen Chandran, Sailendrakumar Kolatt Yiannakas, Adonis Gould, Nathaniel Khamaisy, Mohammad Rosenblum, Kobi eLife Neuroscience To survive in an ever-changing environment, animals must detect and learn salient information. The anterior insular cortex (aIC) and medial prefrontal cortex (mPFC) are heavily implicated in salience and novelty processing, and specifically, the processing of taste sensory information. Here, we examined the role of aIC-mPFC reciprocal connectivity in novel taste neophobia and memory formation, in mice. Using pERK and neuronal intrinsic properties as markers for neuronal activation, and retrograde AAV (rAAV) constructs for connectivity, we demonstrate a correlation between aIC-mPFC activity and novel taste experience. Furthermore, by expressing inhibitory chemogenetic receptors in these projections, we show that aIC-to-mPFC activity is necessary for both taste neophobia and its attenuation. However, activity within mPFC-to-aIC projections is essential only for the neophobic reaction but not for the learning process. These results provide an insight into the cortical circuitry needed to detect, react to- and learn salient stimuli, a process critically involved in psychiatric disorders. eLife Sciences Publications, Ltd 2021-07-05 /pmc/articles/PMC8282338/ /pubmed/34219650 http://dx.doi.org/10.7554/eLife.66686 Text en © 2021, Kayyal et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Kayyal, Haneen
Chandran, Sailendrakumar Kolatt
Yiannakas, Adonis
Gould, Nathaniel
Khamaisy, Mohammad
Rosenblum, Kobi
Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title_full Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title_fullStr Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title_full_unstemmed Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title_short Insula to mPFC reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
title_sort insula to mpfc reciprocal connectivity differentially underlies novel taste neophobic response and learning in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282338/
https://www.ncbi.nlm.nih.gov/pubmed/34219650
http://dx.doi.org/10.7554/eLife.66686
work_keys_str_mv AT kayyalhaneen insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice
AT chandransailendrakumarkolatt insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice
AT yiannakasadonis insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice
AT gouldnathaniel insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice
AT khamaisymohammad insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice
AT rosenblumkobi insulatompfcreciprocalconnectivitydifferentiallyunderliesnoveltasteneophobicresponseandlearninginmice