Br. Smith et al., The effects of the GABA(B) agonist baclofen on the temporal and structuralcharacteristics of ethanol intake, ALCOHOL, 17(3), 1999, pp. 231-240
The present study examined the behavioral processes mediating the influence
of the GABAB agonist baclofen on the maintenance of voluntary ethanol inta
ke. Long-Evans rats were randomly assigned to two groups, one receiving bac
lofen (10 mg/kg, IF) and the other an equal Volume of saline. Subjects were
presented with a free choice of ethanol (10% v/v) and water immediately fo
llowing drug injections, which occurred every other day. The results demons
trated that baclofen treatment resulted in an overall increase in the-intak
e of absolute ethanol but failed to influence the intake of water. In contr
ast, food intake was substantially attenuated as evidenced by a decrease in
the number of pellets consumed in subjects treated with baclofen. A microa
nalysis of the patterns of food and fluid bouts indicated that the enhanced
ethanol intake was primarily a function of an increase in the frequency of
ethanol bouts. In contrast, the decrease in food intake appeared to be a r
eflection of a decrease in the size of the food meals but not their frequen
cy. An analysis of the temporal pattern of intake over the 23-h test sessio
ns indicated that baclofen treatment produced a biphasic effect on ethanol
intake with a slight decrease in intake during the first hour following tre
atment. Baclofen-treated animals then were observed to consume greater amou
nts of ethanol than did saline controls throughout the remainder of the dar
k cycle as well as into the light cycle. Although ethanol intake gradually
decreased in controls throughout the light cycle, baclofen-treated subjects
maintained a consistent level of intake throughout this period. Furthermor
e, there was a clear dissociation between the temporal pattern of ethanol i
ntake and that of food and water, as intake of the latter substances was sh
own to decrease during the first hour following injection, but unlike with
ethanol, no increase in intake was observed during the remainder of the tes
t session. The nature of the effects of baclofen observed in the present st
udy would suggest that the GABA, receptor system may not play a central rol
e in the mediation of voluntary ethanol intake. (C) 1999 Elsevier Science I
nc. All rights reserved.