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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/71726

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network_name_str CONICET Digital (CONICET)
spelling 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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