GLUTAMATE (glu), an excitatory amino acid (EAA) abundantly present in
the brain of mammals, is also a neurotoxin. We examined lipid peroxida
tion (LPO) potential and antioxidant parameters of midbrain region (MB
R) and frontal cortex of adult rats following treatment with monosodiu
m glutamate (MSG) during postnatal day (PND) 1 through PND 10 at a dai
ly dose of 4 mg g(-1) body weight. In PND 90 rats MSG increased LPO by
56% and altered antioxidant status of MBR. This indicates that oxidat
ive stress produced by glu in vulnerable brain regions may persist for
prolonged periods and could be one of the mechanisms of EAA neurotoxi
city resulting in chronic neurodegeneration.