Background: This study examines the effects of long-term continuous exposur
e to light on dopaminergic supersensitivity induced by repented treatment w
ith haloperidol in rats,
Methods: Spontaneous general activity in an open-field (SGA) and stereotype
d behavior induced by apomorphine (SB-APO) or amphetamine (SB-AMP) were use
d as experimental parameters. Rats were allocated to four groups in each ex
periment: saline-treated animals kept under a 12-hour light/dark cycle (LD)
or 24-hour light/light cycle (LL), and 2 mg/kg haloperidol-treated animals
kept under the above cycles. Plasma corticosterone concentration was also
measured by radioimunoassay in saline-treated mts kept under a LD or LL cyc
le.
Results: All the behavioral parameters used showed the development of centr
al dopaminergic supersensitivity in rats kept under both cycles. Continuous
exposure to light enhanced SGA and SB-AMP in both saline- and haloperidol-
treated mts, but did not modify SB-APO. Animals kept under the LL cycle pre
sented an increased plasma corticosterone concentration.
Conclusions: Our results suggest that continuous exposure to light leads to
an increase in dopaminergic function in both normal and "supersensitive" r
ats. This effect seems to be mediated by a presynaptic mechanism possibly i
nvolving corticosterone actions. (C) 1999 Society of Biological Psychiatry.