The present study assessed the ability of the serotonin reuptake inhib
itor fluoxetine (FLX) and lithium chloride (LiCl) to induce conditione
d taste aversion (CTA) to a novel 20% sucrose solution. FLX (2, 5, or
8 mg/kg) or LiCl (10 mg/kg) was administered 30 min after an initial e
xposure to the solution. A single-bottle test of CTA 24 h after the in
itial exposure indicated that rats that received FLX, at any dose, or
LiCl consumed significantly less solution than did those that received
a vehicle treatment following the initial exposure. To examine the po
ssibility that decreased consumption during the CTA test exposure was
associated with lasting hypophagia and/or hypodipsia induced by FLX, s
eparate groups of rats, without any prior exposure to the solution, we
re administered FLX (2, 5, or 8 mg/kg) and given access 24 h later to
a 20% sucrose solution. FLX failed to suppress consumption of the solu
tion at any dose. These data suggest that FLX induces an aversive drug
state in rats, similar to that induced by LiCl, which serves as a pot
ent conditioned stimulus in CTA. In addition, this CTA is independent
of FLX-induced hypophagia and/or hypodipsia. The relevance of these re
sults to the study of hypophagia induced by FLX administration is disc
ussed.