Effort-related effects of chronic administration of the DA D


Journal

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

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 06 04 2023
accepted: 27 07 2023
medline: 19 9 2023
pubmed: 24 8 2023
entrez: 24 8 2023
Statut: ppublish

Résumé

Long-acting antipsychotics such as haloperidol decanoate are becoming more commonly used. Long-acting depot formulations have several advantages, but secondary negative effects of prolonged delivery, including motivational dysfunctions, could have debilitating effects. Assessing the behavioral changes that emerge during chronic antipsychotic administration in rats could provide insight regarding the development of motivational dysfunctions and drug tolerance. Acute administration of dopamine D2 antagonists such as haloperidol induce motivational deficits in rats, as marked by a shift towards a low-effort bias during effort-based choice tasks. In the present studies, programmable subcutaneous infusion pumps provided continuous and controlled drug delivery of haloperidol. Animals were assessed using a fixed ratio (FR) 5 lever pressing schedule and the FR5/chow feeding test of effort-based choice. The adenosine A Continuous chronic infusions of haloperidol produced significant reductions in FR5 performance and a shift from lever pressing to chow intake in rats tested on FR5/chow feeding choice, with no evidence of tolerance over the 4-week infusion period. Behavior returned to baseline during the vehicle-infusion washout period. Istradefylline significantly reversed the effects of haloperidol, increasing lever pressing and decreasing chow intake in haloperidol-treated rats. These studies provide an important behavioral characterization of the effects of chronically infused haloperidol, and demonstrate that A

Identifiants

pubmed: 37615683
doi: 10.1007/s00213-023-06439-y
pii: 10.1007/s00213-023-06439-y
doi:

Substances chimiques

Haloperidol J6292F8L3D
istradefylline 2GZ0LIK7T4
Antipsychotic Agents 0
Purines 0
Adenosine K72T3FS567

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2173-2185

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Renee A Rotolo (RA)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.
Present Address: Sage Therapeutics, Cambridge, MA, USA.

Alev Ecevitoglu (A)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.

Rose E Presby (RE)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.
Present Address: Scintillon Institute, San Diego, CA, USA.

Hanna Lindgren (H)

Symptom Biology, H. Lundbeck A/S, Ottiliavej 9, 2500, Valby, Denmark.

Cedric Mombereau (C)

Area de Psicobiologia, Universitat Jaume I, Castelló, Spain.

Cyrene Nicholas (C)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.

Alana Moore (A)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.

Gayle A Edelstein (GA)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA.

Merce Correa (M)

Area de Psicobiologia, Universitat Jaume I, Castelló, Spain.

John D Salamone (JD)

Behavioral Neuroscience, Department of Psychological Sciences, University of Connecticut, Storrs, CT, 06269-1020, USA. john.salamone@uconn.edu.

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