Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors

The dopamine D4 receptor (D4R) is predominantly expressed in the prefrontal cortex, a brain area that integrates motor, rewarding, and cognitive information. Because participation of D4Rs in executive learning is largely unknown, we challenged D4R knockout mice (Drd4 -/- ) and their wild-type (WT) l...

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Autores principales: Nemirovsky, S.I., Avale, M.E., Brunner, D., Rubinstein, M.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_08874476_v63_n11_p991_Nemirovsky
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spelling todo:paper_08874476_v63_n11_p991_Nemirovsky2023-10-03T15:40:56Z Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors Nemirovsky, S.I. Avale, M.E. Brunner, D. Rubinstein, M. 6-hydroxydopamine ADHD D4R knockout mouse Dopamine dopamine 4 receptor oxidopamine animal experiment article controlled study discrimination learning learning male mouse nonhuman prefrontal cortex priority journal protein expression reinforcement reward wild type Adrenergic Agents Animals Conditioning, Operant Dopamine Male Mice Mice, Knockout Oxidopamine Prefrontal Cortex Receptors, Dopamine D4 Reward The dopamine D4 receptor (D4R) is predominantly expressed in the prefrontal cortex, a brain area that integrates motor, rewarding, and cognitive information. Because participation of D4Rs in executive learning is largely unknown, we challenged D4R knockout mice (Drd4 -/- ) and their wild-type (WT) littermates, neonatally treated with 6-hydroxydopamine (6-OHDA; icv) or vehicle in two operant learning paradigms. A continuous reinforcement task, in which one food-pellet was delivered after every lever press, showed that 6-OHDA-treated mice (hypodopaminergic) WT mice pressed the reinforcing lever at much lower rates than normodopaminergic WT mice. In contrast, Drd4 -/- mice displayed increased lever pressing rates, regardless of their dopamine content. In another study, mice were trained to solve an operant two-choice task in which a first showing lever was coupled to the delivery of one food pellet only after a second lever emerged. Interval between presentation of both levers was initially 12 s and progressively shortened to 6, 2, and finally 0.5 s. Normodopaminergic WT mice obtained a pellet reward in more than 75% of the trials at 12, 6, and 2 s, whereas hypodopaminergic WT mice were severely impaired to select the reward-paired lever. Absence of D4Rs was not detrimental in this task. Moreover, hypodopaminergic Drd4 -/- mice were as efficient as their normodopaminergic Drd4 -/- siblings in selecting the reward-paired lever. In summary, hypodopaminergic mice exhibit severe impairments to retrieve rewards in two operant positive reinforcement tasks, but these deleterious effects are totally prevented in the absence of functional D4Rs. © 2009 Wiley-Liss, Inc. Fil:Nemirovsky, S.I. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Avale, M.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Rubinstein, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_08874476_v63_n11_p991_Nemirovsky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 6-hydroxydopamine
ADHD
D4R knockout mouse
Dopamine
dopamine 4 receptor
oxidopamine
animal experiment
article
controlled study
discrimination learning
learning
male
mouse
nonhuman
prefrontal cortex
priority journal
protein expression
reinforcement
reward
wild type
Adrenergic Agents
Animals
Conditioning, Operant
Dopamine
Male
Mice
Mice, Knockout
Oxidopamine
Prefrontal Cortex
Receptors, Dopamine D4
Reward
spellingShingle 6-hydroxydopamine
ADHD
D4R knockout mouse
Dopamine
dopamine 4 receptor
oxidopamine
animal experiment
article
controlled study
discrimination learning
learning
male
mouse
nonhuman
prefrontal cortex
priority journal
protein expression
reinforcement
reward
wild type
Adrenergic Agents
Animals
Conditioning, Operant
Dopamine
Male
Mice
Mice, Knockout
Oxidopamine
Prefrontal Cortex
Receptors, Dopamine D4
Reward
Nemirovsky, S.I.
Avale, M.E.
Brunner, D.
Rubinstein, M.
Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
topic_facet 6-hydroxydopamine
ADHD
D4R knockout mouse
Dopamine
dopamine 4 receptor
oxidopamine
animal experiment
article
controlled study
discrimination learning
learning
male
mouse
nonhuman
prefrontal cortex
priority journal
protein expression
reinforcement
reward
wild type
Adrenergic Agents
Animals
Conditioning, Operant
Dopamine
Male
Mice
Mice, Knockout
Oxidopamine
Prefrontal Cortex
Receptors, Dopamine D4
Reward
description The dopamine D4 receptor (D4R) is predominantly expressed in the prefrontal cortex, a brain area that integrates motor, rewarding, and cognitive information. Because participation of D4Rs in executive learning is largely unknown, we challenged D4R knockout mice (Drd4 -/- ) and their wild-type (WT) littermates, neonatally treated with 6-hydroxydopamine (6-OHDA; icv) or vehicle in two operant learning paradigms. A continuous reinforcement task, in which one food-pellet was delivered after every lever press, showed that 6-OHDA-treated mice (hypodopaminergic) WT mice pressed the reinforcing lever at much lower rates than normodopaminergic WT mice. In contrast, Drd4 -/- mice displayed increased lever pressing rates, regardless of their dopamine content. In another study, mice were trained to solve an operant two-choice task in which a first showing lever was coupled to the delivery of one food pellet only after a second lever emerged. Interval between presentation of both levers was initially 12 s and progressively shortened to 6, 2, and finally 0.5 s. Normodopaminergic WT mice obtained a pellet reward in more than 75% of the trials at 12, 6, and 2 s, whereas hypodopaminergic WT mice were severely impaired to select the reward-paired lever. Absence of D4Rs was not detrimental in this task. Moreover, hypodopaminergic Drd4 -/- mice were as efficient as their normodopaminergic Drd4 -/- siblings in selecting the reward-paired lever. In summary, hypodopaminergic mice exhibit severe impairments to retrieve rewards in two operant positive reinforcement tasks, but these deleterious effects are totally prevented in the absence of functional D4Rs. © 2009 Wiley-Liss, Inc.
format JOUR
author Nemirovsky, S.I.
Avale, M.E.
Brunner, D.
Rubinstein, M.
author_facet Nemirovsky, S.I.
Avale, M.E.
Brunner, D.
Rubinstein, M.
author_sort Nemirovsky, S.I.
title Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
title_short Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
title_full Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
title_fullStr Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
title_full_unstemmed Reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine D4 receptors
title_sort reward-seeking and discrimination deficits displayed by hypodopaminergic mice are prevented in mice lacking dopamine d4 receptors
url http://hdl.handle.net/20.500.12110/paper_08874476_v63_n11_p991_Nemirovsky
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AT brunnerd rewardseekinganddiscriminationdeficitsdisplayedbyhypodopaminergicmicearepreventedinmicelackingdopamined4receptors
AT rubinsteinm rewardseekinganddiscriminationdeficitsdisplayedbyhypodopaminergicmicearepreventedinmicelackingdopamined4receptors
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