Differential effects of chronic adolescent glucocorticoid or methamphetamine on drug-induced locomotor hyperactivity and disruption of prepulse inhibition in adulthood in mice.


Journal

Progress in neuro-psychopharmacology & biological psychiatry
ISSN: 1878-4216
Titre abrégé: Prog Neuropsychopharmacol Biol Psychiatry
Pays: England
ID NLM: 8211617

Informations de publication

Date de publication:
13 07 2022
Historique:
received: 08 12 2021
revised: 17 03 2022
accepted: 17 03 2022
pubmed: 27 3 2022
medline: 18 5 2022
entrez: 26 3 2022
Statut: ppublish

Résumé

Sensitization of dopaminergic activity has been suggested as an underlying mechanism in the psychotic symptoms of schizophrenia. Adolescent stress and chronic abuse of methamphetamine (Meth) are well-known risk factors for psychosis and schizophrenia; however it remains unknown how these factors compare in terms of dopaminergic behavioural sensitization in adulthood. In addition, while Brain-Derived Neurotrophic Factor (BDNF) has been implicated in dopaminergic activity and schizophrenia, its role in behavioural sensitization remains unclear. In this study we therefore compared the effect of chronic adolescent treatment with the stress hormone, corticosterone (Cort), or with Meth, on drug-induced locomotor hyperactivity and disruption of prepulse inhibition in adulthood in BDNF heterozygous mice and their wild-type controls, as well as on dopamine receptor gene expression. Between 6 and 9 weeks of age, the animals either received Cort in the drinking water or were treated with an escalating Meth dose protocol. In adulthood, Cort-pretreated mice showed significantly reduced Meth-induced locomotor hyperactivity compared to vehicle-pretreated mice. In contrast, Meth hyperlocomotion was significantly enhanced in animals pretreated with the drug in adolescence. There were no effects of either pretreatment on prepulse inhibition. BDNF Het mice showed greater Meth-induced hyperlocomotion and lower prepulse inhibition than WT mice. There were no effects of either pretreatment on D1 or D2 gene expression in either the dorsal or ventral striatum, while D3 mRNA was shown to be reduced in male mice only irrespective of genotype. These results suggest that in adolescence, chronically elevated glucocorticoid levels, a component of chronic stress, do not cause dopaminergic sensitization adulthood, in contrast to the effect of chronic Meth treatment in the same age period. BDNF does not appear to be involved in the effects of chronic Cort or chronic Meth.

Identifiants

pubmed: 35337859
pii: S0278-5846(22)00044-6
doi: 10.1016/j.pnpbp.2022.110552
pii:
doi:

Substances chimiques

Brain-Derived Neurotrophic Factor 0
Glucocorticoids 0
Methamphetamine 44RAL3456C
Dopamine VTD58H1Z2X
Corticosterone W980KJ009P

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

110552

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Lina Schonfeld (L)

Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Melbourne, Australia.

Emily J Jaehne (EJ)

Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Melbourne, Australia.

Alexandra R Ogden (AR)

Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Melbourne, Australia.

Jereme G Spiers (JG)

Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Australia.

Samuel Hogarth (S)

Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Melbourne, Australia.

Maarten van den Buuse (M)

Department of Psychology and Counselling, School of Psychology and Public Health, La Trobe University, Melbourne, Australia; Department of Pharmacology, University of Melbourne, Australia; College of Public Health, Medical and Veterinary Sciences, James Cook University, Townsville, Australia. Electronic address: m.vandenbuuse@latrobe.edu.au.

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Classifications MeSH