Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice
- Autores
- Cunningham, Christopher L.; Howard, MacKenzie A.; Gill, Sylvia J.; Rubinstein, Marcelo; Low, Malcolm J.; Grandy, David K.
- Año de publicación
- 2000
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Pharmacological blockade studies have supported a role of the dopamine system in ethanol reward for many years, but receptor subtype specificity has been difficult to establish. Recently, genetically engineered mice lacking functional dopamine D2 receptors have been shown to drink less ethanol in a two-bottle choice task. To determine whether reduced ethanol intake reflects a reduction in ethanol reward, D2 receptor-deficient [knockout (KO)] mice were compared to heterozygous (HET) and wild-type (WT; C57BL/6 × DBA/2 F2 hybrid) mice in a place conditioning task. Under conditions that produced reliable place preference in both WT and HET mice, KO mice showed no evidence of place conditioning, suggesting that D2 receptor gene inactivation reduced ethanol reward or the ability to learn about ethanol reward. Consistent with previous findings, this mutation also produced a gene dose-related reduction in basal activity levels. Moreover, KO and HET mice showed enhancement of ethanol-stimulated activity relative to WT mice. However, differences in basal and ethanol-stimulated activity did not explain the differences in place conditioning. Overall, this study strongly supports the conclusion that dopamine D2 receptors normally influence ethanol reward in mice.
Fil: Cunningham, Christopher L.. University of Oregon; Estados Unidos
Fil: Howard, MacKenzie A.. University of Oregon; Estados Unidos
Fil: Gill, Sylvia J.. University of Oregon; 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: Low, Malcolm J.. University of Oregon; Estados Unidos
Fil: Grandy, David K.. University of Oregon; Estados Unidos - Materia
-
C57bl/6&Times;Dba/2 F2 Hybrid Mice
Conditioned Place Preference
Dopamine D2 Receptor
Ethanol
Knockout Mice
Locomotor Activity - 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:11336/71726
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Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient miceCunningham, Christopher L.Howard, MacKenzie A.Gill, Sylvia J.Rubinstein, MarceloLow, Malcolm J.Grandy, David K.C57bl/6&Times;Dba/2 F2 Hybrid MiceConditioned Place PreferenceDopamine D2 ReceptorEthanolKnockout MiceLocomotor Activityhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Pharmacological blockade studies have supported a role of the dopamine system in ethanol reward for many years, but receptor subtype specificity has been difficult to establish. Recently, genetically engineered mice lacking functional dopamine D2 receptors have been shown to drink less ethanol in a two-bottle choice task. To determine whether reduced ethanol intake reflects a reduction in ethanol reward, D2 receptor-deficient [knockout (KO)] mice were compared to heterozygous (HET) and wild-type (WT; C57BL/6 × DBA/2 F2 hybrid) mice in a place conditioning task. Under conditions that produced reliable place preference in both WT and HET mice, KO mice showed no evidence of place conditioning, suggesting that D2 receptor gene inactivation reduced ethanol reward or the ability to learn about ethanol reward. Consistent with previous findings, this mutation also produced a gene dose-related reduction in basal activity levels. Moreover, KO and HET mice showed enhancement of ethanol-stimulated activity relative to WT mice. However, differences in basal and ethanol-stimulated activity did not explain the differences in place conditioning. Overall, this study strongly supports the conclusion that dopamine D2 receptors normally influence ethanol reward in mice.Fil: Cunningham, Christopher L.. University of Oregon; Estados UnidosFil: Howard, MacKenzie A.. University of Oregon; Estados UnidosFil: Gill, Sylvia J.. University of Oregon; 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: Low, Malcolm J.. University of Oregon; Estados UnidosFil: Grandy, David K.. University of Oregon; Estados UnidosPergamon-Elsevier Science Ltd2000-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/71726Cunningham, Christopher L.; Howard, MacKenzie A.; Gill, Sylvia J.; Rubinstein, Marcelo; Low, Malcolm J.; et al.; Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice; Pergamon-Elsevier Science Ltd; Pharmacology Biochemistry and Behavior; 67; 4; 12-2000; 693-6990091-3057CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/S0091-3057(00)00414-7info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0091305700004147info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:21:58Zoai:ri.conicet.gov.ar:11336/71726instacron: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:34982025-09-29 10:21:58.806CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
title |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
spellingShingle |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice Cunningham, Christopher L. C57bl/6&Times;Dba/2 F2 Hybrid Mice Conditioned Place Preference Dopamine D2 Receptor Ethanol Knockout Mice Locomotor Activity |
title_short |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
title_full |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
title_fullStr |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
title_full_unstemmed |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
title_sort |
Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice |
dc.creator.none.fl_str_mv |
Cunningham, Christopher L. Howard, MacKenzie A. Gill, Sylvia J. Rubinstein, Marcelo Low, Malcolm J. Grandy, David K. |
author |
Cunningham, Christopher L. |
author_facet |
Cunningham, Christopher L. Howard, MacKenzie A. Gill, Sylvia J. Rubinstein, Marcelo Low, Malcolm J. Grandy, David K. |
author_role |
author |
author2 |
Howard, MacKenzie A. Gill, Sylvia J. Rubinstein, Marcelo Low, Malcolm J. Grandy, David K. |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
C57bl/6&Times;Dba/2 F2 Hybrid Mice Conditioned Place Preference Dopamine D2 Receptor Ethanol Knockout Mice Locomotor Activity |
topic |
C57bl/6&Times;Dba/2 F2 Hybrid Mice Conditioned Place Preference Dopamine D2 Receptor Ethanol Knockout Mice Locomotor Activity |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Pharmacological blockade studies have supported a role of the dopamine system in ethanol reward for many years, but receptor subtype specificity has been difficult to establish. Recently, genetically engineered mice lacking functional dopamine D2 receptors have been shown to drink less ethanol in a two-bottle choice task. To determine whether reduced ethanol intake reflects a reduction in ethanol reward, D2 receptor-deficient [knockout (KO)] mice were compared to heterozygous (HET) and wild-type (WT; C57BL/6 × DBA/2 F2 hybrid) mice in a place conditioning task. Under conditions that produced reliable place preference in both WT and HET mice, KO mice showed no evidence of place conditioning, suggesting that D2 receptor gene inactivation reduced ethanol reward or the ability to learn about ethanol reward. Consistent with previous findings, this mutation also produced a gene dose-related reduction in basal activity levels. Moreover, KO and HET mice showed enhancement of ethanol-stimulated activity relative to WT mice. However, differences in basal and ethanol-stimulated activity did not explain the differences in place conditioning. Overall, this study strongly supports the conclusion that dopamine D2 receptors normally influence ethanol reward in mice. Fil: Cunningham, Christopher L.. University of Oregon; Estados Unidos Fil: Howard, MacKenzie A.. University of Oregon; Estados Unidos Fil: Gill, Sylvia J.. University of Oregon; 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: Low, Malcolm J.. University of Oregon; Estados Unidos Fil: Grandy, David K.. University of Oregon; Estados Unidos |
description |
Pharmacological blockade studies have supported a role of the dopamine system in ethanol reward for many years, but receptor subtype specificity has been difficult to establish. Recently, genetically engineered mice lacking functional dopamine D2 receptors have been shown to drink less ethanol in a two-bottle choice task. To determine whether reduced ethanol intake reflects a reduction in ethanol reward, D2 receptor-deficient [knockout (KO)] mice were compared to heterozygous (HET) and wild-type (WT; C57BL/6 × DBA/2 F2 hybrid) mice in a place conditioning task. Under conditions that produced reliable place preference in both WT and HET mice, KO mice showed no evidence of place conditioning, suggesting that D2 receptor gene inactivation reduced ethanol reward or the ability to learn about ethanol reward. Consistent with previous findings, this mutation also produced a gene dose-related reduction in basal activity levels. Moreover, KO and HET mice showed enhancement of ethanol-stimulated activity relative to WT mice. However, differences in basal and ethanol-stimulated activity did not explain the differences in place conditioning. Overall, this study strongly supports the conclusion that dopamine D2 receptors normally influence ethanol reward in mice. |
publishDate |
2000 |
dc.date.none.fl_str_mv |
2000-12 |
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/11336/71726 Cunningham, Christopher L.; Howard, MacKenzie A.; Gill, Sylvia J.; Rubinstein, Marcelo; Low, Malcolm J.; et al.; Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice; Pergamon-Elsevier Science Ltd; Pharmacology Biochemistry and Behavior; 67; 4; 12-2000; 693-699 0091-3057 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/71726 |
identifier_str_mv |
Cunningham, Christopher L.; Howard, MacKenzie A.; Gill, Sylvia J.; Rubinstein, Marcelo; Low, Malcolm J.; et al.; Ethanol-conditioned place preference is reduced in dopamine D2 receptor-deficient mice; Pergamon-Elsevier Science Ltd; Pharmacology Biochemistry and Behavior; 67; 4; 12-2000; 693-699 0091-3057 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/S0091-3057(00)00414-7 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0091305700004147 |
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 |
Pergamon-Elsevier Science Ltd |
publisher.none.fl_str_mv |
Pergamon-Elsevier Science Ltd |
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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1844614210102755328 |
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13.070432 |