id paper:paper_00333158_v163_n1_p54_Chausmer
record_format dspace
spelling paper:paper_00333158_v163_n1_p54_Chausmer2023-06-08T15:00:27Z Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice Rubinstein, Marcelo Cocaine D2 Dopamine Drug discrimination Knockout Locomotor activity Raclopride cocaine dopamine 2 receptor raclopride sodium chloride animal experiment article controlled study discriminative stimulus dopaminergic system dose response drug discrimination drug effect drug receptor binding genotype knockout mouse locomotion mouse nonhuman priority journal receptor blocking Animals Cocaine Discrimination (Psychology) Dopamine Antagonists Dopamine Uptake Inhibitors Dose-Response Relationship, Drug Female Genotype Male Mice Mice, Knockout Motor Activity Raclopride Receptors, Dopamine D2 Rationale: Dopamine (DA) D2-like antagonists block several effects of cocaine, including its locomotor stimulant and interoceptive discriminative-stimulus effects. Because these compounds generally lack selectivity among the D2-like DA receptors, the specific roles of the subtypes remain unclear. Objectives: DA D2 receptor knockout (DA D2R KO), heterozygous (HET), and wild-type (WT) mice were used to study the role of D2 DA receptors in the effects of cocaine. Some effects of the relatively selective DA D2-like antagonist raclopride were also studied to further assess the role of D2 receptors. Methods: DA D2R KO, HET, and WT mice were treated with cocaine (1-10 mg/kg) or vehicle, and their horizontal locomotor activity was assessed. The mice were also trained to discriminate i.p. injections of saline from cocaine (10 mg/kg) using a two-response key, fixed-ratio-20 response, food-reinforcement procedure. A range of doses of cocaine (1.0-17 mg/kg) was administered before 15-min test sessions. Results: Both DA D2R KO and HET mice showed reduced levels of horizontal activity relative to WT mice. Cocaine dose dependently stimulated activity in each genotype, with the highest level of activity induced in the DA D2R WT mice. All three genotypes acquired the discrimination of 10 mg/kg cocaine; tested doses of 1.0-10.0 mg/kg produced dose-related increases in the number of cocaine-appropriate responses. Raclopride, at inactive to fully active doses (0.1-1.0 mg/kg), did not fully substitute for cocaine. Raclopride dose dependently shifted the cocaine dose-effect curve to the right in DA D2R WT and HET mice. However, in DA D2R KO mice, raclopride was inactive as an antagonist. Conclusions: The present data indicate an involvement of D2 DA receptors in the locomotor-stimulating effects and the interoceptive discriminative-stimulus effects of cocaine in WT subjects. However, the D2 receptor is not necessary for the effects, suggesting redundant dopaminergic mechanisms for the discriminative-stimulus interoceptive effects of cocaine. Fil:Rubinstein, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2002 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00333158_v163_n1_p54_Chausmer http://hdl.handle.net/20.500.12110/paper_00333158_v163_n1_p54_Chausmer
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cocaine
D2
Dopamine
Drug discrimination
Knockout
Locomotor activity
Raclopride
cocaine
dopamine 2 receptor
raclopride
sodium chloride
animal experiment
article
controlled study
discriminative stimulus
dopaminergic system
dose response
drug discrimination
drug effect
drug receptor binding
genotype
knockout mouse
locomotion
mouse
nonhuman
priority journal
receptor blocking
Animals
Cocaine
Discrimination (Psychology)
Dopamine Antagonists
Dopamine Uptake Inhibitors
Dose-Response Relationship, Drug
Female
Genotype
Male
Mice
Mice, Knockout
Motor Activity
Raclopride
Receptors, Dopamine D2
spellingShingle Cocaine
D2
Dopamine
Drug discrimination
Knockout
Locomotor activity
Raclopride
cocaine
dopamine 2 receptor
raclopride
sodium chloride
animal experiment
article
controlled study
discriminative stimulus
dopaminergic system
dose response
drug discrimination
drug effect
drug receptor binding
genotype
knockout mouse
locomotion
mouse
nonhuman
priority journal
receptor blocking
Animals
Cocaine
Discrimination (Psychology)
Dopamine Antagonists
Dopamine Uptake Inhibitors
Dose-Response Relationship, Drug
Female
Genotype
Male
Mice
Mice, Knockout
Motor Activity
Raclopride
Receptors, Dopamine D2
Rubinstein, Marcelo
Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
topic_facet Cocaine
D2
Dopamine
Drug discrimination
Knockout
Locomotor activity
Raclopride
cocaine
dopamine 2 receptor
raclopride
sodium chloride
animal experiment
article
controlled study
discriminative stimulus
dopaminergic system
dose response
drug discrimination
drug effect
drug receptor binding
genotype
knockout mouse
locomotion
mouse
nonhuman
priority journal
receptor blocking
Animals
Cocaine
Discrimination (Psychology)
Dopamine Antagonists
Dopamine Uptake Inhibitors
Dose-Response Relationship, Drug
Female
Genotype
Male
Mice
Mice, Knockout
Motor Activity
Raclopride
Receptors, Dopamine D2
description Rationale: Dopamine (DA) D2-like antagonists block several effects of cocaine, including its locomotor stimulant and interoceptive discriminative-stimulus effects. Because these compounds generally lack selectivity among the D2-like DA receptors, the specific roles of the subtypes remain unclear. Objectives: DA D2 receptor knockout (DA D2R KO), heterozygous (HET), and wild-type (WT) mice were used to study the role of D2 DA receptors in the effects of cocaine. Some effects of the relatively selective DA D2-like antagonist raclopride were also studied to further assess the role of D2 receptors. Methods: DA D2R KO, HET, and WT mice were treated with cocaine (1-10 mg/kg) or vehicle, and their horizontal locomotor activity was assessed. The mice were also trained to discriminate i.p. injections of saline from cocaine (10 mg/kg) using a two-response key, fixed-ratio-20 response, food-reinforcement procedure. A range of doses of cocaine (1.0-17 mg/kg) was administered before 15-min test sessions. Results: Both DA D2R KO and HET mice showed reduced levels of horizontal activity relative to WT mice. Cocaine dose dependently stimulated activity in each genotype, with the highest level of activity induced in the DA D2R WT mice. All three genotypes acquired the discrimination of 10 mg/kg cocaine; tested doses of 1.0-10.0 mg/kg produced dose-related increases in the number of cocaine-appropriate responses. Raclopride, at inactive to fully active doses (0.1-1.0 mg/kg), did not fully substitute for cocaine. Raclopride dose dependently shifted the cocaine dose-effect curve to the right in DA D2R WT and HET mice. However, in DA D2R KO mice, raclopride was inactive as an antagonist. Conclusions: The present data indicate an involvement of D2 DA receptors in the locomotor-stimulating effects and the interoceptive discriminative-stimulus effects of cocaine in WT subjects. However, the D2 receptor is not necessary for the effects, suggesting redundant dopaminergic mechanisms for the discriminative-stimulus interoceptive effects of cocaine.
author Rubinstein, Marcelo
author_facet Rubinstein, Marcelo
author_sort Rubinstein, Marcelo
title Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
title_short Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
title_full Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
title_fullStr Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
title_full_unstemmed Cocaine-induced locomotor activity and cocaine discrimination in dopamine D2 receptor mutant mice
title_sort cocaine-induced locomotor activity and cocaine discrimination in dopamine d2 receptor mutant mice
publishDate 2002
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00333158_v163_n1_p54_Chausmer
http://hdl.handle.net/20.500.12110/paper_00333158_v163_n1_p54_Chausmer
work_keys_str_mv AT rubinsteinmarcelo cocaineinducedlocomotoractivityandcocainediscriminationindopamined2receptormutantmice
_version_ 1768544630018670592