Differential sensitivity of ethanol-elicited ERK phosphorylation in nucleus accumbens of Sardinian alcohol-preferring and -non preferring rats

• Published in: Alcohol (Fayetteville, N.Y.) N.Y.), 2014-08, Vol.48 (5), p.471-476
• Main Authors: Rosas, Michela, Zaru, Alessandro, Sabariego, Marta, Giugliano, Valentina, Carboni, Ezio, Colombo, Giancarlo, Acquas, Elio
• Format: Article
• Language: English
• Subjects: Alcohol; Alcoholism; Amygdala - drug effects; Amygdala - metabolism; Animals; Behavior; Ethanol; Ethanol - pharmacology; Extracellular Signal-Regulated MAP Kinases - metabolism; Laboratory animals; Liver cirrhosis; Male; Mortality; Nucleus accumbens (Acb); Nucleus Accumbens - drug effects; Nucleus Accumbens - metabolism; Phosphorylated extracellular signal regulated kinase (pERK); Phosphorylation; Prefrontal Cortex - drug effects; Prefrontal Cortex - metabolism; Psychiatry; Rats; Rodents; Sardinian alcohol-preferring (sP) and -non preferring rats (sNP); Septal Nuclei - metabolism; Signal transduction; Studies
• ISSN: 0741-8329; 1873-6823
• DOI: 10.1016/j.alcohol.2014.04.002

Abstract Sardinian alcohol-preferring (sP) and -non preferring (sNP) rats have been selectively bred for opposite ethanol preference and consumption; sP rats represent a validated experimental tool to model several aspects of excessive ethanol drinking in humans. Phosphorylated Extracellular signal-Regulated Kinase (pERK) in dopamine-rich terminal areas plays a critical role in several psychopharmacological effects of addictive drugs, including ethanol. This study was aimed at investigating whether ethanol-elicited ERK activation may differ in key brain areas of ethanol-naïve sP and sNP rats. To this end, the effects of ethanol (0, 0.5, 1, and 2 g/kg, administered intra-gastrically [i.g.]) on ERK phosphorylation were assessed by pERK immunohistochemistry in the shell (AcbSh) and core (AcbC) of the nucleus accumbens (Acb) as well as in the prelimbic (PrL) and infralimbic (IL) prefrontal cortex (PFCx), in the bed nucleus of stria terminalis (BSTL) and in the central nucleus of the amygdala (CeA). Ethanol (1 g/kg) significantly increased pERK immunoreactivity in AcbSh and AcbC of sP but not sNP rats. Conversely, ethanol failed to affect pERK expression in PrL and IL PFCx as well as in BSTL and CeA of both sP and sNP rats. These results suggest that selective breeding of these rat lines results in differential effects of acute ethanol on ERK phosphorylation in brain regions critical for the psychopharmacological effects of ethanol.