Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors
- Autores
- Shin, Jung Hoon; Adrover, Martín Federico; Alvarez, Verónica Elizabeth
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Nucleus accumbens (NAc) shell shows unique dopamine (DA) signals in vivo and plays a unique role in DA-dependent behaviors such as reward-motivated learning and the response to drugs of abuse.Adisynaptic mechanism forDArelease was reported and shown to require synchronized firing of cholinergic interneurons (CINs) and activation of nicotinic acetylcholine (ACh) receptors (nAChRs) inDAneuron (DAN) axons. The properties of this disynaptic mechanism of DA transmission are not well understood in the NAc shell. In this study, in vitro fast-scan cyclic voltammetry was used to examine the modulation of DA transmission evoked by CINs firing in the shell of mice and compared with other striatal regions.Wefound thatDAsignals in the shell displayed significant degree of summation in response to train stimulation of CINs, contrary to core and dorsal striatum. The summation was amplified by a D2-like receptor antagonist and experiments with mice with targeted deletion of D2 receptors to DANs or CINs revealed that D2 receptors in CINs mediate a fast inhibition observed within 100 ms of the first pulse, whereas D2 autoreceptors in DAN terminals are engaged in a slower inhibition that peaks at ~500 ms.AChalso contributes to the use-dependent inhibition ofDArelease through muscarinic receptors only in the shell, where higher activity of acetylcholinesterase minimizes nAChR desensitization and promotes summation. These findings show that DA signals are modulated differentially by endogenous DA and ACh in the shell, which may underlie the unique features of shell DA signals in vivo.Significance Statement The present study reports that dopamine (DA) release evoked by activation of cholinergic interneurons displays a high degree of summation in the shell and shows unique modulation by endogenousDAand acetylcholine. Desensitization of nicotinic receptors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also minimal in the shell in part due to elevated acetylcholinesterase activity. This distinctive modulation of DA transmission in the shell may have functional implications in the acquisition of reward-motivated behaviors and reward seeking.
Fil: Shin, Jung Hoon. National Institutes of Health; Estados Unidos
Fil: Adrover, Martín Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. National Institutes of Health; Estados Unidos
Fil: Alvarez, Verónica Elizabeth. National Institutes of Health; Estados Unidos - Materia
-
D2 RECEPTORS
G-PROTEIN COUPLED RECEPTORS
MUSCARINIC RECEPTORS
NICOTINIC RECEPTORS
OPTOGENETICS
VOLTAMMETRY - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/66715
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/66715 |
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CONICET Digital (CONICET) |
spelling |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptorsShin, Jung HoonAdrover, Martín FedericoAlvarez, Verónica ElizabethD2 RECEPTORSG-PROTEIN COUPLED RECEPTORSMUSCARINIC RECEPTORSNICOTINIC RECEPTORSOPTOGENETICSVOLTAMMETRYhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Nucleus accumbens (NAc) shell shows unique dopamine (DA) signals in vivo and plays a unique role in DA-dependent behaviors such as reward-motivated learning and the response to drugs of abuse.Adisynaptic mechanism forDArelease was reported and shown to require synchronized firing of cholinergic interneurons (CINs) and activation of nicotinic acetylcholine (ACh) receptors (nAChRs) inDAneuron (DAN) axons. The properties of this disynaptic mechanism of DA transmission are not well understood in the NAc shell. In this study, in vitro fast-scan cyclic voltammetry was used to examine the modulation of DA transmission evoked by CINs firing in the shell of mice and compared with other striatal regions.Wefound thatDAsignals in the shell displayed significant degree of summation in response to train stimulation of CINs, contrary to core and dorsal striatum. The summation was amplified by a D2-like receptor antagonist and experiments with mice with targeted deletion of D2 receptors to DANs or CINs revealed that D2 receptors in CINs mediate a fast inhibition observed within 100 ms of the first pulse, whereas D2 autoreceptors in DAN terminals are engaged in a slower inhibition that peaks at ~500 ms.AChalso contributes to the use-dependent inhibition ofDArelease through muscarinic receptors only in the shell, where higher activity of acetylcholinesterase minimizes nAChR desensitization and promotes summation. These findings show that DA signals are modulated differentially by endogenous DA and ACh in the shell, which may underlie the unique features of shell DA signals in vivo.Significance Statement The present study reports that dopamine (DA) release evoked by activation of cholinergic interneurons displays a high degree of summation in the shell and shows unique modulation by endogenousDAand acetylcholine. Desensitization of nicotinic receptors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also minimal in the shell in part due to elevated acetylcholinesterase activity. This distinctive modulation of DA transmission in the shell may have functional implications in the acquisition of reward-motivated behaviors and reward seeking.Fil: Shin, Jung Hoon. National Institutes of Health; Estados UnidosFil: Adrover, Martín Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. National Institutes of Health; Estados UnidosFil: Alvarez, Verónica Elizabeth. National Institutes of Health; Estados UnidosSociety for Neuroscience2017-11-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/66715Shin, Jung Hoon; Adrover, Martín Federico; Alvarez, Verónica Elizabeth; Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors; Society for Neuroscience; Journal of Neuroscience; 37; 46; 15-11-2017; 11166-111800270-6474CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1523/JNEUROSCI.0596-17.2017info:eu-repo/semantics/altIdentifier/url/http://www.jneurosci.org/content/37/46/11166info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:22:04Zoai:ri.conicet.gov.ar:11336/66715instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:22:04.692CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
title |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
spellingShingle |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors Shin, Jung Hoon D2 RECEPTORS G-PROTEIN COUPLED RECEPTORS MUSCARINIC RECEPTORS NICOTINIC RECEPTORS OPTOGENETICS VOLTAMMETRY |
title_short |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
title_full |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
title_fullStr |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
title_full_unstemmed |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
title_sort |
Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors |
dc.creator.none.fl_str_mv |
Shin, Jung Hoon Adrover, Martín Federico Alvarez, Verónica Elizabeth |
author |
Shin, Jung Hoon |
author_facet |
Shin, Jung Hoon Adrover, Martín Federico Alvarez, Verónica Elizabeth |
author_role |
author |
author2 |
Adrover, Martín Federico Alvarez, Verónica Elizabeth |
author2_role |
author author |
dc.subject.none.fl_str_mv |
D2 RECEPTORS G-PROTEIN COUPLED RECEPTORS MUSCARINIC RECEPTORS NICOTINIC RECEPTORS OPTOGENETICS VOLTAMMETRY |
topic |
D2 RECEPTORS G-PROTEIN COUPLED RECEPTORS MUSCARINIC RECEPTORS NICOTINIC RECEPTORS OPTOGENETICS VOLTAMMETRY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Nucleus accumbens (NAc) shell shows unique dopamine (DA) signals in vivo and plays a unique role in DA-dependent behaviors such as reward-motivated learning and the response to drugs of abuse.Adisynaptic mechanism forDArelease was reported and shown to require synchronized firing of cholinergic interneurons (CINs) and activation of nicotinic acetylcholine (ACh) receptors (nAChRs) inDAneuron (DAN) axons. The properties of this disynaptic mechanism of DA transmission are not well understood in the NAc shell. In this study, in vitro fast-scan cyclic voltammetry was used to examine the modulation of DA transmission evoked by CINs firing in the shell of mice and compared with other striatal regions.Wefound thatDAsignals in the shell displayed significant degree of summation in response to train stimulation of CINs, contrary to core and dorsal striatum. The summation was amplified by a D2-like receptor antagonist and experiments with mice with targeted deletion of D2 receptors to DANs or CINs revealed that D2 receptors in CINs mediate a fast inhibition observed within 100 ms of the first pulse, whereas D2 autoreceptors in DAN terminals are engaged in a slower inhibition that peaks at ~500 ms.AChalso contributes to the use-dependent inhibition ofDArelease through muscarinic receptors only in the shell, where higher activity of acetylcholinesterase minimizes nAChR desensitization and promotes summation. These findings show that DA signals are modulated differentially by endogenous DA and ACh in the shell, which may underlie the unique features of shell DA signals in vivo.Significance Statement The present study reports that dopamine (DA) release evoked by activation of cholinergic interneurons displays a high degree of summation in the shell and shows unique modulation by endogenousDAand acetylcholine. Desensitization of nicotinic receptors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also minimal in the shell in part due to elevated acetylcholinesterase activity. This distinctive modulation of DA transmission in the shell may have functional implications in the acquisition of reward-motivated behaviors and reward seeking. Fil: Shin, Jung Hoon. National Institutes of Health; Estados Unidos Fil: Adrover, Martín Federico. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. National Institutes of Health; Estados Unidos Fil: Alvarez, Verónica Elizabeth. National Institutes of Health; Estados Unidos |
description |
Nucleus accumbens (NAc) shell shows unique dopamine (DA) signals in vivo and plays a unique role in DA-dependent behaviors such as reward-motivated learning and the response to drugs of abuse.Adisynaptic mechanism forDArelease was reported and shown to require synchronized firing of cholinergic interneurons (CINs) and activation of nicotinic acetylcholine (ACh) receptors (nAChRs) inDAneuron (DAN) axons. The properties of this disynaptic mechanism of DA transmission are not well understood in the NAc shell. In this study, in vitro fast-scan cyclic voltammetry was used to examine the modulation of DA transmission evoked by CINs firing in the shell of mice and compared with other striatal regions.Wefound thatDAsignals in the shell displayed significant degree of summation in response to train stimulation of CINs, contrary to core and dorsal striatum. The summation was amplified by a D2-like receptor antagonist and experiments with mice with targeted deletion of D2 receptors to DANs or CINs revealed that D2 receptors in CINs mediate a fast inhibition observed within 100 ms of the first pulse, whereas D2 autoreceptors in DAN terminals are engaged in a slower inhibition that peaks at ~500 ms.AChalso contributes to the use-dependent inhibition ofDArelease through muscarinic receptors only in the shell, where higher activity of acetylcholinesterase minimizes nAChR desensitization and promotes summation. These findings show that DA signals are modulated differentially by endogenous DA and ACh in the shell, which may underlie the unique features of shell DA signals in vivo.Significance Statement The present study reports that dopamine (DA) release evoked by activation of cholinergic interneurons displays a high degree of summation in the shell and shows unique modulation by endogenousDAand acetylcholine. Desensitization of nicotinic receptors, which is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also minimal in the shell in part due to elevated acetylcholinesterase activity. This distinctive modulation of DA transmission in the shell may have functional implications in the acquisition of reward-motivated behaviors and reward seeking. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-11-15 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/66715 Shin, Jung Hoon; Adrover, Martín Federico; Alvarez, Verónica Elizabeth; Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors; Society for Neuroscience; Journal of Neuroscience; 37; 46; 15-11-2017; 11166-11180 0270-6474 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/66715 |
identifier_str_mv |
Shin, Jung Hoon; Adrover, Martín Federico; Alvarez, Verónica Elizabeth; Distinctive modulation of dopamine release in the nucleus accumbens shell mediated by dopamine and acetylcholine receptors; Society for Neuroscience; Journal of Neuroscience; 37; 46; 15-11-2017; 11166-11180 0270-6474 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1523/JNEUROSCI.0596-17.2017 info:eu-repo/semantics/altIdentifier/url/http://www.jneurosci.org/content/37/46/11166 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Society for Neuroscience |
publisher.none.fl_str_mv |
Society for Neuroscience |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846781733110808576 |
score |
12.928904 |