Literature DB >> 28456841

Changes in gene expression and sensitivity of cocaine reward produced by a continuous fat diet.

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

Abstract

RATIONALE: Preclinical studies report that free access to a high-fat diet (HFD) alters the response to psychostimulants.
OBJECTIVES: The aim of the present study was to examine how HFD exposure during adolescence modifies cocaine effects. Gene expression of CB1 and mu-opioid receptors (MOr) in the nucleus accumbens (N Acc) and prefrontal cortex (PFC) and ghrelin receptor (GHSR) in the ventral tegmental area (VTA) were assessed.
METHODS: Mice were allowed continuous access to fat from PND 29, and the locomotor (10 mg/kg) and reinforcing effects of cocaine (1 and 6 mg/kg) on conditioned place preference (CPP) were evaluated on PND 69. Another group of mice was exposed to a standard diet until the day of post-conditioning, on which free access to the HFD began.
RESULTS: HFD induced an increase of MOr gene expression in the N Acc, but decreased CB1 receptor in the N Acc and PFC. After fat withdrawal, the reduction of CB1 receptor in the N Acc was maintained. Gene expression of GHSR in the VTA decreased during the HFD and increased after withdrawal. Following fat discontinuation, mice exhibited increased anxiety, augmented locomotor response to cocaine, and developed CPP for 1 mg/kg cocaine. HFD reduced the number of sessions required to extinguish the preference and decreased sensitivity to drug priming-induced reinstatement.
CONCLUSION: Our results suggest that consumption of a HFD during adolescence induces neurobiochemical changes that increased sensitivity to cocaine when fat is withdrawn, acting as an alternative reward.

Entities:  

Keywords:  CB1; Cocaine; Conditioned place preference; High-fat diet; Mu-opioid receptor

Mesh:

Substances:

Year:  2017        PMID: 28456841     DOI: 10.1007/s00213-017-4630-9

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


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