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Reduction of Cocaine-Induced Locomotor Effects by Enriched Environment Is Associated with Cell-Specific Accumulation of ΔFosB in Striatal and Cortical Subregions

  • Audrey Lafragette
  • , Michael T. Bardo
  • , Virginie Lardeux
  • , Marcello Solinas
  • , Nathalie Thiriet

Producción científica: Articlerevisión exhaustiva

16 Citas (Scopus)

Resumen

Background: Early exposure to enriched environments has been shown to decrease the locomotor effects induced by repeated injections of cocaine and modify basal and cocaine-induced total protein levels of the transcription factor ΔFosB in the whole striatum of mice. In this study, we aimed at characterizing whether the profile of ΔFosB accumulation induced by enriched environments and cocaine would be similar or different in terms of brain areas and cell type. Methods: We used mice expressing the eGFP protein in D1 receptor positive (D1R(+)) neurons to determine whether Δ FosB induced by enriched environment or cocaine injections (5×15 mg/kg) would occur in selective subpopulations of neurons in several subregions of the striatum and prefrontal cortex. Results: We found that: (1) exposure to enriched environment reduces cocaine-induced locomotor activation, confirming our previous findings; (2) exposure to enriched environment by itself increases the accumulation of Δ FosB mostly in D1R(-) cells in the shell part of the nucleus accumbens and dorsal striatum, whereas in the nucleus accumbens core, Δ FosB accumulates in both D1R(+) and D1R(-) neurons; (3) in standard environment mice, cocaine induces accumulation of Δ FosB selectively in D1R(+) cells in the nucleus accumbens, dorsal striatum, and infralimbic cortex; and (4) the effects of enriched environments and cocaine on accumulation of Δ FosB were reciprocally blocked by their combination. Conclusions: Altogether, these results suggest that the enriched environment-induced reduction in behavioral effects of cocaine might result from 2 distinct effects on ΔFosB in striatal medium-sized spiny neurons belonging to the direct and indirect pathways.

Idioma originalEnglish
Páginas (desde-hasta)237-246
Número de páginas10
PublicaciónInternational Journal of Neuropsychopharmacology
Volumen20
N.º3
DOI
EstadoPublished - 2017

Nota bibliográfica

Publisher Copyright:
© The Author 2016. Published by Oxford University Press on behalf of CINP.

Financiación

This work was supported by INSERM, University of Poitiers, Mission Interministérielle de la Lutte contre les Drogues et la Toxicomanie (MILDT-INSERM), and Région Poitou-Charentes. A. Lafragette is a recipient of a PhD fellowship from French ministry of research. M. T. Bardo was supported by the U.S. Public Health Service (grants nos. P50 DA 05312, R01 DA12964) and visiting professor grant from the “région Poitou-Charentes.”

FinanciadoresNúmero del financiador
French ministry of research
MILDT-INSERM
Mission Interministérielle de la Lutte contre les Drogues et la Toxicomanie
Région Poitou-Charentes
University of Poitiers
National Institute on Drug AbuseR01DA012964
National Institute on Drug Abuse
U.S. Public Health ServiceP50 DA 05312, R01 DA12964
U.S. Public Health Service
Institut national de la santé et de la recherche médicale

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • General Medicine

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