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. 2014 Oct 6;142(2):361–374. doi: 10.1093/toxsci/kfu184

TABLE 4.

Expression of Genes Associated with Fibrosis

Genes AlbCre+/caNrf2−
AlbCre+/caNrf2+
Dietary Effect
Genetic Effect
Std Chow MCD Std Chow MCD AlbCre+/caNrf2- AlbCre+/caNrf2+ Std Chow MCD
Columns 1 2 3 4 1 versus 2 3 versus 4 1 versus 3 2 versus 4
COL1A1 1.00 ± 0.11 0.80 ± 0.11 1.45 ± 0.29 1.13 ± 0.22
TIMP1 1.00 ± 0.09 5.25 ± 0.82* 1.75 ± 0.50 3.74 ± 0.53* 5.25 2.14
TIMP2 1.00 ± 0.08 1.05 ± 0.12 1.12 ± 0.13 1.03 ± 0.09
MMP2 1.00 ± 0.14 0.99 ± 0.11 1.39 ± 0.10 1.26 ± 0.20
MMP9 1.00 ± 0.09 0.91 ± 0.09 1.27 ± 0.28 0.96 ± 0.11

qRT-PCR was performed for genes associated with fibrosis using RNAs from AlbCre+/caNrf2− versus AlbCre+/caNrf2+ animals on MCD diet after 28 days. The mRNA levels are first normalized to the β-actin mRNA content of each sample, and each experimental group is then normalized to the AlbCre+/caNrf2−, standard chow group. All data are presented as mean ± SEM. N = 6–8 for each of the 4 groups. The fold changes in mRNA abundance were compared between groups using one-way ANOVA with Fisher’s LSD post hoc test. Significant fold changes are presented on the right side of the table. *P < 0.05 when compared with standard chow of the same genotype. **P < 0.05 when compared with AlbCre+/caNrf2− on the same diet.