Potassium dichromate was given to female Swiss mice (25 mg/kg per day) oral
ly in water for 1-3 days. Brain homogenates were prepared to evaluate the o
ccurrence of oxidative stress in this organ through the measurement of the
antioxidant defense levels, and the extent of lipid peroxidation. In additi
on, mitochondrial fractions were isolated from brain homogenates to determi
ne the production of reactive oxygen species in this subcellular fraction.
The administration of potassium dichromate for 3 days caused increases of 7
2 and 74% in superoxide dismutase and catalase activities, respectively, in
the homogenates. The treatment with this metal for 3 days increased brain
homogenate chemiluminescence and thiobarbituric acid-reactive substances by
34 and 29%, respectively. Thr brain contents of the non-enzymatic antioxid
ants alpha -tocopherol and sulfhydryl groups decreased by 35 and 32%. respe
ctively. Ascorbic acid levels were not modified by the administration of po
tassium dichromate. Finally. there was a significant increment in the mitoc
hondrial production of oxidants in the brain of treated mice as compared wi
th controls. These results suggest that chromium(VI) produces an increased
formation of reactive oxygen species and brain lipid peroxidation. The incr
ease in the antioxidant enzyme activities reflects an adaptive response aga
inst oxidative stress, while the reduction in the levels of non-enzymatic a
ntioxidants might be due to their reaction with reactive oxygen species gen
erated during the metabolism of chromium(VI). (C) 2000 Elsevier Science Ire
land Ltd. All rights reserved.