The effects of Selenium(Se) on central dopaminergic function were exam
ined in male Sprague-Dawley rats. In this experiment, animals were imp
lanted with microdialysis probes and dialysates were analyzed for dopa
mine (DA), 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic aci
d (HVA). After reaching baseline values, sodium selenite was either in
jected intraperitoneally (i.p.) or directly infused into the striatum
(ST) or nucleus accumbens (NA). Se administration of 3.0 mg/kg (i.p.)
significantly increased (70%) DA overflow in the ST. Meanwhile direct
Se perfusion (10 mM) also caused a significant elevation of synaptic D
A concentrations in the ST and NA. Levels of DOPAC and KVA were minima
lly affected in all studies. In order to test for the effects of DA re
ceptor activation, animals were pretreated with quinpirole (0.5 mg/kg,
s.c.), an hour prior to Se (10 mM) infusion through the probe. It was
found that quinpirole pre-treatment reduced Se-induced changes in DA
concentrations. It was concluded from the present study that Se's cent
ral action might be related to its ability to potentiate DA function.