Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels
- Autores
- Martyniuk, Kelly M.; Torres Herraez, Arturo; Lowes, Daniel C.; Rubinstein, Marcelo; Labouesse, Marie A.; Kellendonk, Christoph
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In the striatum, acetylcholine (ACh) neuron activity is modulated co-incident with dopamine (DA) release in response to unpredicted rewards and reward-predicting cues and both neuromodulators are thought to regulate each other. While this co-regulation has been studied using stimulation studies, the existence of this mutual regulation in vivo during natural behavior is still largely unexplored. One long-standing controversy has been whether striatal DA is responsible for the induction of the cholinergic pause or whether DA D2 receptors (D2Rs) modulate a pause that is induced by other mechanisms. Here, we used genetically encoded sensors in combination with pharmacological and genetic inactivation of D2Rs from cholinergic interneurons (CINs) to simultaneously measure ACh and DA levels after CIN D2R inactivation in mice. We found that CIN D2Rs are not necessary for the initiation of cue-induced decrease in ACh levels. Rather, they prolong the duration of the decrease and inhibit ACh rebound levels. Notably, the change in cue-evoked ACh levels is not associated with altered cue-evoked DA release. Moreover, D2R inactivation strongly decreased the temporal correlation between DA and ACh signals not only at cue presentation but also during the intertrial interval pointing to a general mechanism by which D2Rs coordinate both signals. At the behavioral level D2R antagonism increased the latency to lever press, which was not observed in CIN-selective D2R knock out mice. Press latency correlated with the cue-evoked decrease in ACh levels and artificial inhibition of CINs revealed that longer inhibition shortens the latency to press compared to shorter inhibition. This supports a role of the ACh signal and it´s regulation by D2Rs in the motivation to initiate actions.
Fil: Martyniuk, Kelly M.. Columbia University; Estados Unidos
Fil: Torres Herraez, Arturo. Columbia University; Estados Unidos
Fil: Lowes, Daniel C.. Columbia University; Estados Unidos
Fil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Labouesse, Marie A.. Columbia University; Estados Unidos
Fil: Kellendonk, Christoph. Columbia University; Estados Unidos - Materia
-
Drd2
DOPAMINE
ACETYLCHOLINE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/240706
Ver los metadatos del registro completo
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Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levelsMartyniuk, Kelly M.Torres Herraez, ArturoLowes, Daniel C.Rubinstein, MarceloLabouesse, Marie A.Kellendonk, ChristophDrd2DOPAMINEACETYLCHOLINEhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1In the striatum, acetylcholine (ACh) neuron activity is modulated co-incident with dopamine (DA) release in response to unpredicted rewards and reward-predicting cues and both neuromodulators are thought to regulate each other. While this co-regulation has been studied using stimulation studies, the existence of this mutual regulation in vivo during natural behavior is still largely unexplored. One long-standing controversy has been whether striatal DA is responsible for the induction of the cholinergic pause or whether DA D2 receptors (D2Rs) modulate a pause that is induced by other mechanisms. Here, we used genetically encoded sensors in combination with pharmacological and genetic inactivation of D2Rs from cholinergic interneurons (CINs) to simultaneously measure ACh and DA levels after CIN D2R inactivation in mice. We found that CIN D2Rs are not necessary for the initiation of cue-induced decrease in ACh levels. Rather, they prolong the duration of the decrease and inhibit ACh rebound levels. Notably, the change in cue-evoked ACh levels is not associated with altered cue-evoked DA release. Moreover, D2R inactivation strongly decreased the temporal correlation between DA and ACh signals not only at cue presentation but also during the intertrial interval pointing to a general mechanism by which D2Rs coordinate both signals. At the behavioral level D2R antagonism increased the latency to lever press, which was not observed in CIN-selective D2R knock out mice. Press latency correlated with the cue-evoked decrease in ACh levels and artificial inhibition of CINs revealed that longer inhibition shortens the latency to press compared to shorter inhibition. This supports a role of the ACh signal and it´s regulation by D2Rs in the motivation to initiate actions.Fil: Martyniuk, Kelly M.. Columbia University; Estados UnidosFil: Torres Herraez, Arturo. Columbia University; Estados UnidosFil: Lowes, Daniel C.. Columbia University; Estados UnidosFil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Labouesse, Marie A.. Columbia University; Estados UnidosFil: Kellendonk, Christoph. Columbia University; Estados UnidoseLife Sciences2022-07-20info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/240706Martyniuk, Kelly M.; Torres Herraez, Arturo; Lowes, Daniel C.; Rubinstein, Marcelo; Labouesse, Marie A.; et al.; Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels; eLife Sciences; eLife; 11; 20-7-2022; 1-242050-084XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://elifesciences.org/articles/76111info:eu-repo/semantics/altIdentifier/doi/10.7554/eLife.76111info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T10:39:43Zoai:ri.conicet.gov.ar:11336/240706instacron: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:34982025-11-05 10:39:43.452CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| title |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| spellingShingle |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels Martyniuk, Kelly M. Drd2 DOPAMINE ACETYLCHOLINE |
| title_short |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| title_full |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| title_fullStr |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| title_full_unstemmed |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| title_sort |
Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels |
| dc.creator.none.fl_str_mv |
Martyniuk, Kelly M. Torres Herraez, Arturo Lowes, Daniel C. Rubinstein, Marcelo Labouesse, Marie A. Kellendonk, Christoph |
| author |
Martyniuk, Kelly M. |
| author_facet |
Martyniuk, Kelly M. Torres Herraez, Arturo Lowes, Daniel C. Rubinstein, Marcelo Labouesse, Marie A. Kellendonk, Christoph |
| author_role |
author |
| author2 |
Torres Herraez, Arturo Lowes, Daniel C. Rubinstein, Marcelo Labouesse, Marie A. Kellendonk, Christoph |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
Drd2 DOPAMINE ACETYLCHOLINE |
| topic |
Drd2 DOPAMINE ACETYLCHOLINE |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
In the striatum, acetylcholine (ACh) neuron activity is modulated co-incident with dopamine (DA) release in response to unpredicted rewards and reward-predicting cues and both neuromodulators are thought to regulate each other. While this co-regulation has been studied using stimulation studies, the existence of this mutual regulation in vivo during natural behavior is still largely unexplored. One long-standing controversy has been whether striatal DA is responsible for the induction of the cholinergic pause or whether DA D2 receptors (D2Rs) modulate a pause that is induced by other mechanisms. Here, we used genetically encoded sensors in combination with pharmacological and genetic inactivation of D2Rs from cholinergic interneurons (CINs) to simultaneously measure ACh and DA levels after CIN D2R inactivation in mice. We found that CIN D2Rs are not necessary for the initiation of cue-induced decrease in ACh levels. Rather, they prolong the duration of the decrease and inhibit ACh rebound levels. Notably, the change in cue-evoked ACh levels is not associated with altered cue-evoked DA release. Moreover, D2R inactivation strongly decreased the temporal correlation between DA and ACh signals not only at cue presentation but also during the intertrial interval pointing to a general mechanism by which D2Rs coordinate both signals. At the behavioral level D2R antagonism increased the latency to lever press, which was not observed in CIN-selective D2R knock out mice. Press latency correlated with the cue-evoked decrease in ACh levels and artificial inhibition of CINs revealed that longer inhibition shortens the latency to press compared to shorter inhibition. This supports a role of the ACh signal and it´s regulation by D2Rs in the motivation to initiate actions. Fil: Martyniuk, Kelly M.. Columbia University; Estados Unidos Fil: Torres Herraez, Arturo. Columbia University; Estados Unidos Fil: Lowes, Daniel C.. Columbia University; Estados Unidos Fil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Labouesse, Marie A.. Columbia University; Estados Unidos Fil: Kellendonk, Christoph. Columbia University; Estados Unidos |
| description |
In the striatum, acetylcholine (ACh) neuron activity is modulated co-incident with dopamine (DA) release in response to unpredicted rewards and reward-predicting cues and both neuromodulators are thought to regulate each other. While this co-regulation has been studied using stimulation studies, the existence of this mutual regulation in vivo during natural behavior is still largely unexplored. One long-standing controversy has been whether striatal DA is responsible for the induction of the cholinergic pause or whether DA D2 receptors (D2Rs) modulate a pause that is induced by other mechanisms. Here, we used genetically encoded sensors in combination with pharmacological and genetic inactivation of D2Rs from cholinergic interneurons (CINs) to simultaneously measure ACh and DA levels after CIN D2R inactivation in mice. We found that CIN D2Rs are not necessary for the initiation of cue-induced decrease in ACh levels. Rather, they prolong the duration of the decrease and inhibit ACh rebound levels. Notably, the change in cue-evoked ACh levels is not associated with altered cue-evoked DA release. Moreover, D2R inactivation strongly decreased the temporal correlation between DA and ACh signals not only at cue presentation but also during the intertrial interval pointing to a general mechanism by which D2Rs coordinate both signals. At the behavioral level D2R antagonism increased the latency to lever press, which was not observed in CIN-selective D2R knock out mice. Press latency correlated with the cue-evoked decrease in ACh levels and artificial inhibition of CINs revealed that longer inhibition shortens the latency to press compared to shorter inhibition. This supports a role of the ACh signal and it´s regulation by D2Rs in the motivation to initiate actions. |
| publishDate |
2022 |
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2022-07-20 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/240706 Martyniuk, Kelly M.; Torres Herraez, Arturo; Lowes, Daniel C.; Rubinstein, Marcelo; Labouesse, Marie A.; et al.; Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels; eLife Sciences; eLife; 11; 20-7-2022; 1-24 2050-084X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/240706 |
| identifier_str_mv |
Martyniuk, Kelly M.; Torres Herraez, Arturo; Lowes, Daniel C.; Rubinstein, Marcelo; Labouesse, Marie A.; et al.; Dopamine D2Rs coordinate cue-evoked changes in striatal acetylcholine levels; eLife Sciences; eLife; 11; 20-7-2022; 1-24 2050-084X CONICET Digital CONICET |
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eng |
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eng |
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eLife Sciences |
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eLife Sciences |
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