The dopamine depleting agent tetrabenazine alters effort-related decision making as assessed by mouse touchscreen procedures.


Journal

Psychopharmacology
ISSN: 1432-2072
Titre abrégé: Psychopharmacology (Berl)
Pays: Germany
ID NLM: 7608025

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 14 04 2020
accepted: 01 06 2020
pubmed: 21 6 2020
medline: 31 12 2020
entrez: 21 6 2020
Statut: ppublish

Résumé

Effort-based decision-making tasks allow animals to choose between preferred reinforcers that require high effort to obtain vs. low-effort/low reward options. Mesolimbic dopamine (DA) and related neural systems regulate effort-based choice. Tetrabenazine (TBZ) is a vesicular monoamine transport type-2 inhibitor that blocks DA storage and depletes DA. In humans, TBZ induces motivational dysfunction and depression. TBZ has been shown reliably to induce a low-effort bias in rats, but there are fewer mouse studies. The present studies used touchscreen operant procedures (Bussey-Saksida chambers) to assess the effects of TBZ on effort-based choice in mice. C57BL6 mice were trained to press an elevated lit panel on the touchscreen on a fixed ratio 1 schedule reinforced by strawberry milkshake, vs. approaching and consuming a concurrently available but less preferred food pellets (Bio-serv). TBZ (2.0-8.0 mg/kg IP) shifted choice, producing a dose-related decrease in panel pressing but an increase in pellet intake. In contrast, reinforcer devaluation by pre-feeding substantially decreased both panel pressing and pellet intake. In free-feeding choice tests, mice strongly preferred the milkshake vs. the pellets, and TBZ had no effect on milkshake intake or preference, indicating that the TBZ-induced low-effort bias was not due to changes in primary food motivation or preference. TBZ significantly decreased tissue levels of nucleus accumbens DA. The DA depleting agent TBZ induced an effort-related motivational dysfunction in mice, which may have clinical relevance for assessing novel drug targets for their potential use as therapeutic agents in patients with motivation impairments.

Identifiants

pubmed: 32561947
doi: 10.1007/s00213-020-05578-w
pii: 10.1007/s00213-020-05578-w
doi:

Substances chimiques

Adrenergic Uptake Inhibitors 0
Dopamine Antagonists 0
Dopamine VTD58H1Z2X
Tetrabenazine Z9O08YRN8O

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2845-2854

Auteurs

Jen-Hau Yang (JH)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Rose E Presby (RE)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Renee A Rotolo (RA)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Taina Quiles (T)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Kevin Okifo (K)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Emma Zorda (E)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Roslyn Holly Fitch (RH)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.

Mercè Correa (M)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA.
Area de Psicobiologia, Universitat Jaume I, Castelló, Spain.

John D Salamone (JD)

Behavioral Neuroscience Division, Department of Psychological Sciences, University of Connecticut, Storrs, CT, USA. john.salamone@uconn.edu.

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Classifications MeSH