A transcriptional study in mice with different ethanol-drinking profiles: Possible involvement of the GABA(B) receptor
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
30/10/2013
30/10/2013
2012
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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 |
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 |