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. 2014 Dec 15;4:7473. doi: 10.1038/srep07473

Table 1. Biochemical changes in rat hepatic function and oxidant status.

  CON CCl4 ESM
AST (Karmen) 56.12 ± 2.34a 207.79 ± 25.0b 111.68 ± 17.94c
ALT (Karmen) 8.09 ± 0.93a 38.40 ± 7.81b 18.98 ± 4.63c
Albumin (g/dL) 4.70 ± 0.21 4.84 ± 0.21 4.45 ± 0.11
Total protein (g/dL) 6.95 ± 0.17 7.12 ± 0.37 6.69 ± 0.14
TBARS (μM) 3.92 ± 0.29a 5.11 ± 0.46b 3.97 ± 0.31a
Liver TBARS (μmol/g liver) 0.46 ± 0.02a 0.74 ± 0.05b 0.60 ± 0.03c
Hyaluronic acid (ng/ml) 45.28 ± 6.96a 77.11 ± 13.14b 60.30 ± 13.21ab
Timp1 (ng/ml) 3.74 ± 0.23a 5.76 ± 0.31b 4.81 ± 0.32c
PIIINP (ng/ml) 0.53 ± 0.10a 0.91 ± 0.11b 0.78 ± 0.10ab
ELF score 5.59 ± 0.20a 6.69 ± 0.24b 6.15 ± 0.24ab

CON, control rats; CCl4, rats administered CCl4; ESM, rats given CCl4 and ESM (20 g kg−1); AST, aspartate aminotransferase; ALT, alanine aminotransferase; TBARS, thiobarbituric acid reactive substances; TIMP1, tissue metallopeptidase inhibitor 1; PIIINP, amino-terminal propeptide of type III procollagen, ELF, enhanced liver fibrosis. Data are expressed as mean ± SE in each group (n = 6). Data with different letters (a,b,c) in the same column are significantly different at P < 0.05 by Dunnett's test.