FI and SV contributed equally to this work.
Ethanol-Induced Extracellular Signal Regulated Kinase: Role of Dopamine D1 Receptors
Article first published online: 16 MAR 2009
Copyright © 2009 by the Research Society on Alcoholism
Alcoholism: Clinical and Experimental Research
Volume 33, Issue 5, pages 858–867, May 2009
How to Cite
Ibba, F., Vinci, S., Spiga, S., Peana, A. T., Assaretti, A. R., Spina, L., Longoni, R. and Acquas, E. (2009), Ethanol-Induced Extracellular Signal Regulated Kinase: Role of Dopamine D1 Receptors. Alcoholism: Clinical and Experimental Research, 33: 858–867. doi: 10.1111/j.1530-0277.2009.00907.x
- Issue published online: 13 APR 2009
- Article first published online: 16 MAR 2009
- Received for publication June 17, 2008; accepted December 11, 2008.
- Extended Amygdala;
- Nucleus Accumbens;
Background: Addictive drugs activate extracellular signal regulated kinase (ERK) in brain regions critically involved in their affective and motivational properties. The aim of this study was to demonstrate the ethanol-induced activation of ERK in the nucleus accumbens (Acb) and in the extended amygdala [bed nucleus of the stria terminalis lateralis (BSTL) and central nucleus of the amygdala (CeA)] and to highlight the role of dopamine (DA) D1 receptors in these effects.
Methods: Ethanol (0.5, 1, and 2 g/kg) was administered by gavage and ERK phosphorylation was determined in the nucleus Acb (shell and core), BSTL, and CeA by immunohistochemistry. The DA D1 receptor antagonist, SCH 39166 (SCH) (50 μg/kg), was administered 10 minutes before ethanol (1 g/kg).
Results: Quantitative microscopic examination showed that ethanol, dose-dependently increased phospho-ERK immunoreactivity (optical and neuronal densities) in the shell and core of nucleus Acb, BSTL, and CeA. Pretreatment with SCH fully prevented the increases elicited by ethanol (1 g/kg) in all brain regions studied.
Conclusions: The results of this study indicate that ethanol, similar to other addictive drugs, activates ERK in nucleus Acb and extended amygdala via a DA D1 receptor-mediated mechanism. Overall, these results suggest that the D1 receptors/ERK pathway may play a critical role in the motivational properties of ethanol.