Table 3.
Effect of acute exposure to diesel exhaust on lipid peroxidation in mouse brain
| Sex | Treatment | OB | HIP | CB | CX | ST |
|---|---|---|---|---|---|---|
| M | FA | 5.0 ± 0.1 | 4.4 ± 0.1 | 3.6 ± 0.2 | 3.0 ± 0.2 | 2.2 ± 0.1 |
| DE | 30.1 ± 1.7** | 13.0 ± 0.3* | 6.3 ± 0.1* | 4.1 ± 0.2 | 6.1 ± 0.1* | |
| (% of FA) | 602 | 295 | 175 | 137 | 277 | |
| F | FA | 2.3 ± 0.1 | 1.1 ± 0.1 | 5.9 ± 0.1 | 4.4 ± 0.1 | 2.6 ± 0.1 |
| DE | 8.4 ± 0.1*,## | 2.5 ± 0.1*,# | 8.8 ± 0.1* | 6.7 ± 0.1 | 3.1 ± 0.2# | |
| (% of FA) | 365 | 227 | 149 | 152 | 119 |
Levels of malonyldialdehyde (MDA, nmol/g) are shown as a measurement of lipid peroxidation. Wild-type male (M) and female (F) mice were exposed to diesel exhaust (DE; 250–300 µg/m3) or filtered air (FA) for 6 h, as described in Methods. Results represent the mean (± SE) of three animals/group analyzed in duplicate. Results were analyzed for statistical significance by one-way ANOVA with Bonferroni correction for multiple comparisons; DE vs FA:
p<0.05;
p<0.01; Female vs. male,
p,0.05,
p<0.01.
OB, olfactory bulb; HIP, hippocampus; CB, cerebellum, CX, cerebral cortex; ST, striatum.