Literature DB >> 28457972

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

M Carmen Blanco-Gandía1, Juan Carlos Ledesma1, Auxiliadora Aracil-Fernández2, Francisco Navarrete2, Sandra Montagud-Romero1, Maria A Aguilar1, Jorge Manzanares2, José Miñarro1, Marta Rodríguez-Arias3.   

Abstract

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.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Binge eating; Conditioned place preference; Ethanol; Fat; Gene expression; Self-administration

Mesh:

Substances:

Year:  2017        PMID: 28457972     DOI: 10.1016/j.neuropharm.2017.04.040

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  12 in total

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