A transcriptional study in mice with different ethanol-drinking profiles: Possible involvement of the GABA(B) receptor


Autoria(s): Ribeiro, Andrea Frozino; Correia, Diego; Torres, Adriana Amorim; Villas Boas, Gustavo Roberto; Rueda, André Veloso Lima; Camarini, Rosana; Chiavegatto, Silvana; Boerngen-Lacerda, Roseli; Brunialti-Godard, Ana Lucia
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

30/10/2013

30/10/2013

2012

Resumo

Previous studies have suggested that gamma-aminobutyric acid-B (GABA(B)) receptor agonists effectively reduce ethanol intake. The quantification using real-time polymerase chain reaction of Gabbr1 and Gabbr2 mRNA from the prefrontal cortex, hypothalamus, hippocampus, and striatum in mice exposed to an animal model of the addiction developed in our laboratory was performed to evaluate the involvement of the GABAB receptor in ethanol consumption. We used outbred, Swiss mice exposed to a three-bottle free-choice model (water, 5% v/v ethanol, and 10% v/v ethanol) that consisted of four phases: acquisition (AC), withdrawal (W), reexposure (RE), and quinine-adulteration (AD). Based on individual ethanol intake, the mice were classified into three groups: "addicted" (A group; preference for ethanol and persistent consumption during all phases), "heavy" (H group; preference for ethanol and a reduction in ethanol intake in the AD phase compared to AC phase), and "light" (L group; preference for water during all phases). In the prefrontal cortex in the A group, we found high Gabbr1 and Gabbr2 transcription levels, with significantly higher Gabbr1 transcription levels compared with the C (ethanol-naive control mice). L, and H groups. In the hippocampus in the A group, Gabbr2 mRNA levels were significantly lower compared with the C, L, and H groups. In the striatum, we found a significant increase in Gabbr1 transcription levels compared with the C, L, and H groups. No differences in Gabbr1 or Gabbr2 transcription levels were observed in the hypothalamus among groups. In summary, Gabbr1 and Gabbr2 transcription levels were altered in cerebral areas related to drug taking only in mice behaviorally classified as "addicted" drinkers, suggesting that these genes may contribute to high and persistent ethanol consumption. (C) 2012 Elsevier Inc. All rights reserved.

Conselho Nacional de Pesquisa (CNPq)

Conselho Nacional de Pesquisa (CNPq)

Conselho de Auxilio do Pessoal de Ensino Superior (CAPES)

Conselho de Auxilio do Pessoal de Ensino Superior (CAPES)

Minas Gerais State Foundation (FAPEMIG: EDT Universal ) [01/2008 APQ-00179-08]

Minas Gerais State Foundation (FAPEMIG: EDT Universal )

Identificador

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, OXFORD, v. 102, n. 2, supl., Part 3, pp. 224-232, AUG, 2012

0091-3057

http://www.producao.usp.br/handle/BDPI/36818

10.1016/j.pbb.2012.04.010

http://dx.doi.org/10.1016/j.pbb.2012.04.010

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

OXFORD

Relação

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR

Direitos

closedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #BEHAVIORAL GENETICS #MRNA #ETHANOL CONSUMPTION #ADDICTED #GABA(B) RECEPTOR #MICE #ALCOHOL-PREFERRING RATS #ANIMAL-MODELS #NUCLEUS-ACCUMBENS #DRUG-ADDICTION #PYRAMIDAL NEURONS #NERVOUS-SYSTEM #MESSENGER-RNA #C57BL/6J MICE #DOUBLE-BLIND #B RECEPTORS #BEHAVIORAL SCIENCES #NEUROSCIENCES #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion