Neuropeptides
Volume 44, Issue 5 , Pages 413-420, October 2010

Effects of acute ethanol administration on methionine–enkephalin expression and release in regions of the rat brain

  • M. Méndez

      Affiliations

    • Departamento de Neuroquímica, Subdirección de Investigaciones Clínicas, Instituto Nacional de Psiquiatría Ramón de la Fuente, Calzada México Xochimilco 101, Col. San Lorenzo Huipulco, 14370 México D.F., Mexico
    • Corresponding Author InformationCorresponding author. Tel.: +52 55 41 60 50 91; fax: +52 55 55 13 37 22.
  • ,
  • I.G. Barbosa-Luna

      Affiliations

    • Departamento de Neuroquímica, Subdirección de Investigaciones Clínicas, Instituto Nacional de Psiquiatría Ramón de la Fuente, Calzada México Xochimilco 101, Col. San Lorenzo Huipulco, 14370 México D.F., Mexico
  • ,
  • J.M. Pérez-Luna

      Affiliations

    • Departamento de Neuroquímica, Subdirección de Investigaciones Clínicas, Instituto Nacional de Psiquiatría Ramón de la Fuente, Calzada México Xochimilco 101, Col. San Lorenzo Huipulco, 14370 México D.F., Mexico
  • ,
  • A. Cupo

      Affiliations

    • Institut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique (CNRS), Université de Nice-Sophia-Antipolis, 660 Route des Lucioles, 06560 Valbonne, France
  • ,
  • J. Oikawa

      Affiliations

    • Departamento de Farmacobiología, Centro de Investigación y de Estudios Avanzados, Calzada de los Tenorios 235, Col. Granjas-Coapa, 14330 México D.F., Mexico

Received 11 December 2009; accepted 8 May 2010. published online 02 June 2010.

Abstract 

The dopaminergic mesolimbic system plays a key role in mediating the reinforcing properties of ethanol and other drugs of abuse. Ethanol reinforcement and high alcohol drinking behaviour have been suggested to involve the ethanol-induced activation of endogenous opioid systems. Ethanol may alter opioidergic transmission at different levels, including opioid peptide biosynthesis and release, as well as binding to opioid receptors. The aim of this work was to investigate the effects of different ethanol doses on methionine–enkephalin (Met-enk) release from the rat nucleus accumbens (NAcc). Ethanol effects were also studied on Met-enk content in the NAcc, prefrontal cortex (PFC) and caudate-putamen (CP). Met-enk release was studied by microdialysis in Wistar anesthetized rats and peptide concentrations were quantitated by radioimmunoassay. Ethanol was administered by intraperitoneal injection after a 2-h basal release period. Ethanol doses of 0.5, 1 and 2.5g/kg induced a 2.7-, 4.9- and 3.4-fold increase in Met-enk release from the NAcc. However, ethanol responses followed different kinetics, with earliest effects observed with the highest ethanol dose. In comparison, a 2.5-fold increase in peptide release was produced by 100mM KCl. Ethanol, at a dose of 2.5g/kg, induced a significant 66.7% decrease in Met-enk content in the NAcc, as well as a 76.4% reduction in peptide levels in the CP. Lower ethanol doses did not alter Met-enk content in these regions. On the other hand, an ethanol dose of 0.5g/kg produced a non-significant decrease in Met-enk levels in the PFC. Our results suggest that ethanol-induced changes in enkephalin expression and release in regions of the mesocorticolimbic and nigrostriatal pathways could be involved in ethanol central effects. Released enkephalins by ethanol may modulate the dopaminergic activity of mesolimbic neurons and play a critical role in ethanol reinforcement mechanisms.

Keywords: Ethanol, Opioid peptides, Methionine–enkephalin, Dopaminergic mesocorticolimbic system, Reinforcement, Release

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PII: S0143-4179(10)00050-8

doi:10.1016/j.npep.2010.05.001

Neuropeptides
Volume 44, Issue 5 , Pages 413-420, October 2010