Preference for vigorous exercise versus sedentary sucrose drinking: an animal model of anergia induced by dopamine receptor antagonism.


Journal

Behavioural pharmacology
ISSN: 1473-5849
Titre abrégé: Behav Pharmacol
Pays: England
ID NLM: 9013016

Informations de publication

Date de publication:
09 2020
Historique:
pubmed: 7 3 2020
medline: 3 8 2021
entrez: 7 3 2020
Statut: ppublish

Résumé

Motivation has activational and directional components. Mesolimbic dopamine is critical for the regulation of behavioral activation and effort-related processes in motivated behaviors. Impairing mesolimbic dopamine function leads to fatigue and anergia, but leaves intact other aspects of reinforce seeking behaviors, such as the consummatory or hedonic component. In male Swiss mice, we characterized the impact of dopamine antagonism on the selection of concurrently presented stimuli that have different vigor requirements. We analyzed running wheel activity versus sucrose solution intake, typically used as a measure of anhedonia. Results are compared with data from nonconcurrent presentation to those stimuli. In the concurrent presentation experiment, control mice preferred to spend time running compared to sucrose intake. Dopamine antagonism shifted relative reinforcer preference, reducing time spent on the running wheel, but actually increasing time-consuming sucrose. Mice increased frequency of bouts for both reinforcers, suggesting that there was fatigue in the running wheel rather than aversion. Moreover, satiation or habituation by preexposing animals to both reinforcers did not shift preferences. In the nonconcurrent experiments, haloperidol reduced running wheel but had no impact on sucrose consumption. Dopamine antagonism did not change preference for sucrose or total volume consumed. Additional correlational analyses indicated that baseline differences in sucrose consumption were independent of baseline running or novelty exploration. Thus, dopamine antagonism seems to have anergic rather than anhedonic effects, and the concurrent presentation in this setting could be useful for assessing preferences based on effort requirements.

Identifiants

pubmed: 32141919
doi: 10.1097/FBP.0000000000000556
pii: 00008877-202009000-00005
doi:

Substances chimiques

Dopamine Antagonists 0
Sucrose 57-50-1
Haloperidol J6292F8L3D

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

553-564

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH121350
Pays : United States

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Auteurs

Mercè Correa (M)

Àrea de Psicobiologia, Campus de Riu Sec, Universitat Jaume I, Castelló, Spain.
Department of Psychology, University of Connecticut, Storrs, Connecticut.

Marta Pardo (M)

Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida, USA.

Carla Carratalá-Ros (C)

Àrea de Psicobiologia, Campus de Riu Sec, Universitat Jaume I, Castelló, Spain.

Andrea Martínez-Verdú (A)

Àrea de Psicobiologia, Campus de Riu Sec, Universitat Jaume I, Castelló, Spain.

John D Salamone (JD)

Department of Psychology, University of Connecticut, Storrs, Connecticut.

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