Cargando…

Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning

Processing of contextual information during a new episodic event is crucial for learning and memory. Neuromodulation in the hippocampus and prefrontal cortex plays an important role in the formation of associations between environmental cues and an aversive experience. Noradrenergic neurons in the l...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsetsenis, Theodoros, Badyna, Julia K., Li, Rebecca, Dani, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051520/
https://www.ncbi.nlm.nih.gov/pubmed/35496910
http://dx.doi.org/10.3389/fncel.2022.887679
_version_ 1784696576527040512
author Tsetsenis, Theodoros
Badyna, Julia K.
Li, Rebecca
Dani, John A.
author_facet Tsetsenis, Theodoros
Badyna, Julia K.
Li, Rebecca
Dani, John A.
author_sort Tsetsenis, Theodoros
collection PubMed
description Processing of contextual information during a new episodic event is crucial for learning and memory. Neuromodulation in the hippocampus and prefrontal cortex plays an important role in the formation of associations between environmental cues and an aversive experience. Noradrenergic neurons in the locus coeruleus send dense projections to both regions, but their contribution to contextual associative learning has not been established. Here, we utilize selective optogenetic and pharmacological manipulations to control noradrenergic transmission in the hippocampus during the encoding of a contextual fear memory. We find that boosting noradrenergic terminal release in the dorsal CA1 enhances the acquisition of contextual associative learning and that this effect requires local activation of β-adrenenergic receptors. Moreover, we show that increasing norepinephrine release can ameliorate contextual fear learning impairments caused by dopaminergic dysregulation in the hippocampus. Our data suggest that increasing of hippocampal noradrenergic activity can have important implications in the treatment of cognitive disorders that involve problems in contextual processing.
format Online
Article
Text
id pubmed-9051520
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90515202022-04-30 Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning Tsetsenis, Theodoros Badyna, Julia K. Li, Rebecca Dani, John A. Front Cell Neurosci Cellular Neuroscience Processing of contextual information during a new episodic event is crucial for learning and memory. Neuromodulation in the hippocampus and prefrontal cortex plays an important role in the formation of associations between environmental cues and an aversive experience. Noradrenergic neurons in the locus coeruleus send dense projections to both regions, but their contribution to contextual associative learning has not been established. Here, we utilize selective optogenetic and pharmacological manipulations to control noradrenergic transmission in the hippocampus during the encoding of a contextual fear memory. We find that boosting noradrenergic terminal release in the dorsal CA1 enhances the acquisition of contextual associative learning and that this effect requires local activation of β-adrenenergic receptors. Moreover, we show that increasing norepinephrine release can ameliorate contextual fear learning impairments caused by dopaminergic dysregulation in the hippocampus. Our data suggest that increasing of hippocampal noradrenergic activity can have important implications in the treatment of cognitive disorders that involve problems in contextual processing. Frontiers Media S.A. 2022-04-15 /pmc/articles/PMC9051520/ /pubmed/35496910 http://dx.doi.org/10.3389/fncel.2022.887679 Text en Copyright © 2022 Tsetsenis, Badyna, Li and Dani. 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 Cellular Neuroscience
Tsetsenis, Theodoros
Badyna, Julia K.
Li, Rebecca
Dani, John A.
Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title_full Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title_fullStr Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title_full_unstemmed Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title_short Activation of a Locus Coeruleus to Dorsal Hippocampus Noradrenergic Circuit Facilitates Associative Learning
title_sort activation of a locus coeruleus to dorsal hippocampus noradrenergic circuit facilitates associative learning
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051520/
https://www.ncbi.nlm.nih.gov/pubmed/35496910
http://dx.doi.org/10.3389/fncel.2022.887679
work_keys_str_mv AT tsetsenistheodoros activationofalocuscoeruleustodorsalhippocampusnoradrenergiccircuitfacilitatesassociativelearning
AT badynajuliak activationofalocuscoeruleustodorsalhippocampusnoradrenergiccircuitfacilitatesassociativelearning
AT lirebecca activationofalocuscoeruleustodorsalhippocampusnoradrenergiccircuitfacilitatesassociativelearning
AT danijohna activationofalocuscoeruleustodorsalhippocampusnoradrenergiccircuitfacilitatesassociativelearning