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Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency

The basolateral amygdala (BLA) is critical for associating initially neutral cues with appetitive and aversive stimuli and receives dense neuromodulatory acetylcholine (ACh) projections. We measured BLA ACh signaling and activity of neurons expressing CaMKIIα (a marker for glutamatergic principal ce...

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Autores principales: Crouse, Richard B, Kim, Kristen, Batchelor, Hannah M, Girardi, Eric M, Kamaletdinova, Rufina, Chan, Justin, Rajebhosale, Prithviraj, Pittenger, Steven T, Role, Lorna W, Talmage, David A, Jing, Miao, Li, Yulong, Gao, Xiao-Bing, Mineur, Yann S, Picciotto, Marina R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529459/
https://www.ncbi.nlm.nih.gov/pubmed/32945260
http://dx.doi.org/10.7554/eLife.57335
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author Crouse, Richard B
Kim, Kristen
Batchelor, Hannah M
Girardi, Eric M
Kamaletdinova, Rufina
Chan, Justin
Rajebhosale, Prithviraj
Pittenger, Steven T
Role, Lorna W
Talmage, David A
Jing, Miao
Li, Yulong
Gao, Xiao-Bing
Mineur, Yann S
Picciotto, Marina R
author_facet Crouse, Richard B
Kim, Kristen
Batchelor, Hannah M
Girardi, Eric M
Kamaletdinova, Rufina
Chan, Justin
Rajebhosale, Prithviraj
Pittenger, Steven T
Role, Lorna W
Talmage, David A
Jing, Miao
Li, Yulong
Gao, Xiao-Bing
Mineur, Yann S
Picciotto, Marina R
author_sort Crouse, Richard B
collection PubMed
description The basolateral amygdala (BLA) is critical for associating initially neutral cues with appetitive and aversive stimuli and receives dense neuromodulatory acetylcholine (ACh) projections. We measured BLA ACh signaling and activity of neurons expressing CaMKIIα (a marker for glutamatergic principal cells) in mice during cue-reward learning using a fluorescent ACh sensor and calcium indicators. We found that ACh levels and nucleus basalis of Meynert (NBM) cholinergic terminal activity in the BLA (NBM-BLA) increased sharply in response to reward-related events and shifted as mice learned the cue-reward contingency. BLA CaMKIIα neuron activity followed reward retrieval and moved to the reward-predictive cue after task acquisition. Optical stimulation of cholinergic NBM-BLA terminal fibers led to a quicker acquisition of the cue-reward contingency. These results indicate BLA ACh signaling carries important information about salient events in cue-reward learning and provides a framework for understanding how ACh signaling contributes to shaping BLA responses to emotional stimuli.
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spelling pubmed-75294592020-10-05 Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency Crouse, Richard B Kim, Kristen Batchelor, Hannah M Girardi, Eric M Kamaletdinova, Rufina Chan, Justin Rajebhosale, Prithviraj Pittenger, Steven T Role, Lorna W Talmage, David A Jing, Miao Li, Yulong Gao, Xiao-Bing Mineur, Yann S Picciotto, Marina R eLife Neuroscience The basolateral amygdala (BLA) is critical for associating initially neutral cues with appetitive and aversive stimuli and receives dense neuromodulatory acetylcholine (ACh) projections. We measured BLA ACh signaling and activity of neurons expressing CaMKIIα (a marker for glutamatergic principal cells) in mice during cue-reward learning using a fluorescent ACh sensor and calcium indicators. We found that ACh levels and nucleus basalis of Meynert (NBM) cholinergic terminal activity in the BLA (NBM-BLA) increased sharply in response to reward-related events and shifted as mice learned the cue-reward contingency. BLA CaMKIIα neuron activity followed reward retrieval and moved to the reward-predictive cue after task acquisition. Optical stimulation of cholinergic NBM-BLA terminal fibers led to a quicker acquisition of the cue-reward contingency. These results indicate BLA ACh signaling carries important information about salient events in cue-reward learning and provides a framework for understanding how ACh signaling contributes to shaping BLA responses to emotional stimuli. eLife Sciences Publications, Ltd 2020-09-18 /pmc/articles/PMC7529459/ /pubmed/32945260 http://dx.doi.org/10.7554/eLife.57335 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Neuroscience
Crouse, Richard B
Kim, Kristen
Batchelor, Hannah M
Girardi, Eric M
Kamaletdinova, Rufina
Chan, Justin
Rajebhosale, Prithviraj
Pittenger, Steven T
Role, Lorna W
Talmage, David A
Jing, Miao
Li, Yulong
Gao, Xiao-Bing
Mineur, Yann S
Picciotto, Marina R
Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title_full Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title_fullStr Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title_full_unstemmed Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title_short Acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
title_sort acetylcholine is released in the basolateral amygdala in response to predictors of reward and enhances the learning of cue-reward contingency
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529459/
https://www.ncbi.nlm.nih.gov/pubmed/32945260
http://dx.doi.org/10.7554/eLife.57335
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