The rewarding effects of ethanol are modulated by binge eating of a high-fat diet during adolescence

• Published in: Neuropharmacology Vol. 121; pp. 219 - 230
• Main Authors: Blanco-Gandía, M. Carmen, Ledesma, Juan Carlos, Aracil-Fernández, Auxiliadora, Navarrete, Francisco, Montagud-Romero, Sandra, Aguilar, Maria A., Manzanares, Jorge, Miñarro, José, Rodríguez-Arias, Marta
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 15.07.2017
• Subjects: Animals; Animals, Newborn; Binge eating; Bulimia - physiopathology; Central Nervous System Depressants - pharmacology; Conditioned place preference; Conditioning, Operant - drug effects; Diet, High-Fat; Disease Models, Animal; Drug Administration Routes; Ethanol; Ethanol - pharmacology; Fat; Gene expression; Locomotion - drug effects; Male; Mice; Reward; Self Administration; Time Factors; Fat; Self-administration; Binge eating; Ethanol; Conditioned place preference; Gene expression
• DOI: 10.1016/j.neuropharm.2017.04.040
• ISSN: 0028-3908; 1873-7064

Binge-eating is considered a specific form of overeating characterized by intermittent and high caloric food intake in a short period of time. Epidemiologic studies support a positive relation between the ingestion of fat and ethanol (EtOH), specifically among adolescent subjects. The aim of this work was to clarify the role of the compulsive, limited and intermittent intake of a high-fat food during adolescence on the rewarding effects of EtOH. After binge-eating for 2 h, three days a week from postnatal day (PND) 29, the reinforcing effects of EtOH were tested with EtOH self-administration (SA), conditioned place preference (CPP) and ethanol locomotor sensitization procedures in young adult mice. Animals in the high fat binge (HFB) group that underwent the EtOH SA procedure presented greater EtOH consumption and a higher motivation to obtain the drug. HFB mice also developed preference for the paired compartment in the CPP with a subthreshold dose of EtOH. Independently of the diet, mice developed EtOH-induced locomotor sensitization. After the SA procedure, HFB mice exhibited reduced levels of the mu opioid receptor (MOr) and increased cannabinoid 1 receptor (CB1r) gene expression in the nucleus accumbens (N Acc), and decreased of tyrosine hydroxylase (TH) gene expression in the ventral tegmental area (VTA). Taken together the results suggest that bingeing on fat may represent a vulnerability factor to an escalation of EtOH consumption. •High-fat binge increases EtOH consumption.•High-fat binge induces higher motivation to obtain EtOH.•High-fat binge increases sensitivity to EtOH-induced CPP.•High-fat binge does not alter EtOH-induced locomotor sensitization.•High-fat binge alters MOr, Cb1r and TH gene expression after exposure to EtOH SA.