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Cocaine-induced behavioral sensitization is associated with changes in the expression of endocannabinoid and glutamatergic signaling systems in the mouse prefrontal cortex.

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  • معلومة اضافية
    • Contributors:
      Blanco,E; Pavón,FJ; Palomino,A; Luque-Rojas,MJ; Serrano,A; Rivera,P; Alen,F; Vida,M; Suárez,J; Rodríguez de Fonseca,F Unidad de Gestión Clínica de Salud Mental, Instituto IBIMA-Hospital Regional Universitario de Málaga, Málaga, Spain. Blanco,E Departamento de Psicobiología y Metodología de las Ciencias del Comportamiento, Facultad de Psicología, Universidad de Málaga, Málaga, Spain. Bilbao,A Institute of Psychopharmacology, Central Institute of Mental Health, Medical Faculty of Mannheim, University of Heidelberg, Mannheim, Germany.; This work was supported by Ministerio de Ciencia e Innovación (PI13/02261 and SAF 2010–20521), Instituto de Salud Carlos III (ISCIII), Ministerio de Economía y Competitividad, Red de Trastornos Adictivos (RD12/0028/0001), Plan Nacional Sobre Drogas, Ministerio de Sanidad y Consumo (PNSD2013/049), Consejería de Economía, Innovación y Ciencia, Junta de Andalucía, UE/ERDF (CTS-433 and P-11-CVI-07637), Consejería de Salud, and Junta de Andalucía (PI0232/2008, PI0029/2008 and SAS111224).
    • بيانات النشر:
      Oxford University Press
    • الموضوع:
      2015
    • Collection:
      Sistema Sanitario Público de Andalucía (SSPA): Repositorio
    • نبذة مختصرة :
      Journal Article; Research Support, Non-U.S. Gov't; ; BACKGROUND Endocannabinoids modulate the glutamatergic excitatory transmission by acting as retrograde messengers. A growing body of studies has reported that both signaling systems in the mesocorticolimbic neural circuitry are involved in the neurobiological mechanisms underlying drug addiction. METHODS We investigated whether the expression of both endocannabinoid and glutamatergic systems in the prefrontal cortex (PFC) were altered by an acute and/or repeated cocaine administration schedule that resulted in behavioral sensitization. We measured the protein and mRNA expression of the main endocannabinoid metabolic enzymes and the cannabinoid receptor type 1 (CB1). We also analyzed the mRNA expression of relevant components of the glutamate-signaling system, including glutamate-synthesizing enzymes, metabotropic receptors, and ionotropic receptors. RESULTS Although acute cocaine (10 mg/kg) produced no significant changes in the endocannabinoid-related proteins, repeated cocaine administration (20 mg/kg daily) induced a pronounced increase in the CB1 receptor expression. In addition, acute cocaine administration (10 mg/kg) in cocaine-sensitized mice (referred to as cocaine priming) induced a selective increase in the endocannabinoid-degrading enzymes fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL). These protein changes were accompanied by an overall decrease in the ratios of endocannabinoid synthesis/degradation, especially the N-acyl phosphatidylethanolamine phospholipase D/FAAH and diacylglycerol lipase alpha/MAGL ratios. Regarding mRNA expression, while acute cocaine administration produced a decrease in CB1 receptors and N-acyl phosphatidylethanolamine phospholipase D, repeated cocaine treatment enhanced CB1 receptor expression. Cocaine-sensitized mice that were administered priming injections of cocaine mainly displayed an increased FAAH expression. These endocannabinoid changes were associated with modifications in glutamatergic ...
    • File Description:
      application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
    • ISSN:
      1461-1457
      1469-5111
    • Relation:
      http://ijnp.oxfordjournals.org/content/18/1/pyu024.long; Blanco E, Pavon FJ, Palomino A, Luque-Rojas MJ, Serrano A, Rivera P, et al. Cocaine-induced behavioral sensitization is associated with changes in the expression of endocannabinoid and glutamatergic signaling systems in the mouse prefrontal cortex. Int J Neuropsychopharmacol. 2014;18(1). pii: pyu024.; http://hdl.handle.net/10668/2227; PMC4368868
    • الرقم المعرف:
      10.1093/ijnp/pyu024
    • الدخول الالكتروني :
      http://hdl.handle.net/10668/2227
      https://doi.org/10.1093/ijnp/pyu024
    • Rights:
      open access
    • الرقم المعرف:
      edsbas.D1A05B03