TABLE 1.
Description of liver drug metabolic enzymes | PFOA-treated wild-type mice (fold of change)a | PFOA-treated PPARα knockout mice (fold of change) |
Cytochrome P450, family 1, subfamily a, polypeptide 1 | −2.5 ± 0.45* | No change |
Cytochrome P450, family 1, subfamily a, polypeptide 2 | −3.4 ± 1.14* | No change |
Catechol-o-methyltransferase | −2.1 ± 0.32* | No change |
HSD17β2 | −3.4 ± 0.62* | No change |
HSD17β4 | 3.9 ± 1.05* | No change |
SULT1A1 | −7.1 ± 2.14* | No change |
SULT1E1 | −14.4 ± 1.24* | No change |
Ugt2A1 | −2.3 ± 0.78* | No change |
Ugt2B1 | −2.0 ± 0.31 | No change |
Note. Three-week-old wild-type and PPARα knockout C57Bl/6 mice were treated with vehicle control or PFOA (5 mg/kg) for 4 weeks and sacrificed 24 h after the last treatment. Total RNA was extracted from frozen liver samples and used for the synthesis of first-strand cDNAs that were used for liver drug metabolic enzyme qPCR array analysis as described in the “Materials and Methods” section.
Fold change is expressed as mean ± SD (n = 3).
p < 0.05, compared with respective vehicle control–treated mice.