I. Yokoi et al., EFFECTS OF KYNURENINE METABOLITES ON THE ELECTROCORTICOGRAPHIC ACTIVITY IN THE RAT, Journal of neural transmission, 105(2-3), 1998, pp. 147-160
We examined the effects of kynurenine metabolites administered into th
e right cerebroventricle (1 mu mol) on the electrocorticogram (ECoG) o
f rats to establish the role of kynurenines on brain function. Kynuren
ine, anthranilic acid, quinaldic acid, xanthurenic acid or 8-hydroxyqu
inaldic acid showed no effect on ECoG throughout the recording period
of 4 hours. 3-Hydroxykynurenine had a transient suppressive effect on
the ECoG, while kynurenic acid caused a slight suppression of ECoG act
ivity. 3-Hydroxyanthranilic acid (3-OH-An), a metabolite of 3-hydroxyk
ynurenine, induced spike discharges with a long latency (60-230min). 3
-OH-An is thought to be metabolized to o-aminophenol, 3-methoxyanthran
ilic acid, quinolinic acid, 2-ketoadipic acid and picolinic acid. Amon
g 3-OH-An metabolites, only o-aminophenol induced spike discharges sev
eral minutes after administration, lasting for 60min. On the other han
d, quinolinic acid suppressed ECoG, though 3-methoxyanthranilic acid,
2-ketoadipic acid and picolinic acid had no effects on ECoG. These ele
ctrocorticographic findings suggest that 3-OH-An may induce spike disc
harges after it is metabolized in the brain to o-aminophenol.