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Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle

The olfactory tubercle (OT), which is a component of the olfactory cortex and ventral striatum, has functional domains that play a role in odor-guided motivated behaviors. Learning odor-guided attractive and aversive behavior activates the anteromedial (am) and lateral (l) domains of the OT, respect...

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Autores principales: Sha, Md Fazley Rabbi, Koga, Yuriko, Murata, Yoshihiro, Taniguchi, Mutsuo, Yamaguchi, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480507/
https://www.ncbi.nlm.nih.gov/pubmed/37680965
http://dx.doi.org/10.3389/fnins.2023.1247375
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author Sha, Md Fazley Rabbi
Koga, Yuriko
Murata, Yoshihiro
Taniguchi, Mutsuo
Yamaguchi, Masahiro
author_facet Sha, Md Fazley Rabbi
Koga, Yuriko
Murata, Yoshihiro
Taniguchi, Mutsuo
Yamaguchi, Masahiro
author_sort Sha, Md Fazley Rabbi
collection PubMed
description The olfactory tubercle (OT), which is a component of the olfactory cortex and ventral striatum, has functional domains that play a role in odor-guided motivated behaviors. Learning odor-guided attractive and aversive behavior activates the anteromedial (am) and lateral (l) domains of the OT, respectively. However, the mechanism driving learning-dependent activation of specific OT domains remains unknown. We hypothesized that the neuronal connectivity of OT domains is plastically altered through olfactory experience. To examine the plastic potential of synaptic connections to OT domains, we optogenetically stimulated intracortical inputs from the piriform cortex or sensory inputs from the olfactory bulb to the OT in mice in association with a food reward for attractive learning and electrical foot shock for aversive learning. For both intracortical and sensory connections, axon boutons that terminated in the OT domains were larger in the amOT than in the lOT for mice exhibiting attractive learning and larger in the lOT than in the amOT for mice exhibiting aversive learning. These results indicate that both intracortical and sensory connections to the OT domains have learning-dependent plastic potential, suggesting that this plasticity underlies learning-dependent activation of specific OT domains and the acquisition of appropriate motivated behaviors.
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spelling pubmed-104805072023-09-07 Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle Sha, Md Fazley Rabbi Koga, Yuriko Murata, Yoshihiro Taniguchi, Mutsuo Yamaguchi, Masahiro Front Neurosci Neuroscience The olfactory tubercle (OT), which is a component of the olfactory cortex and ventral striatum, has functional domains that play a role in odor-guided motivated behaviors. Learning odor-guided attractive and aversive behavior activates the anteromedial (am) and lateral (l) domains of the OT, respectively. However, the mechanism driving learning-dependent activation of specific OT domains remains unknown. We hypothesized that the neuronal connectivity of OT domains is plastically altered through olfactory experience. To examine the plastic potential of synaptic connections to OT domains, we optogenetically stimulated intracortical inputs from the piriform cortex or sensory inputs from the olfactory bulb to the OT in mice in association with a food reward for attractive learning and electrical foot shock for aversive learning. For both intracortical and sensory connections, axon boutons that terminated in the OT domains were larger in the amOT than in the lOT for mice exhibiting attractive learning and larger in the lOT than in the amOT for mice exhibiting aversive learning. These results indicate that both intracortical and sensory connections to the OT domains have learning-dependent plastic potential, suggesting that this plasticity underlies learning-dependent activation of specific OT domains and the acquisition of appropriate motivated behaviors. Frontiers Media S.A. 2023-08-23 /pmc/articles/PMC10480507/ /pubmed/37680965 http://dx.doi.org/10.3389/fnins.2023.1247375 Text en Copyright © 2023 Sha, Koga, Murata, Taniguchi and Yamaguchi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Sha, Md Fazley Rabbi
Koga, Yuriko
Murata, Yoshihiro
Taniguchi, Mutsuo
Yamaguchi, Masahiro
Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title_full Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title_fullStr Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title_full_unstemmed Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title_short Learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
title_sort learning-dependent structural plasticity of intracortical and sensory connections to functional domains of the olfactory tubercle
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480507/
https://www.ncbi.nlm.nih.gov/pubmed/37680965
http://dx.doi.org/10.3389/fnins.2023.1247375
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