Table 1.
Effect of crocin treatment on hepatotoxicity markers in a mouse model of TAA-induced liver fibrosis.
Group | ALT | AST | TB | TC | TG |
---|---|---|---|---|---|
U/L | U/L | mg/dL | mg/dL | mg/dL | |
Control | 16.02b ± 4.23 | 13.25b ± 2.04 | 0.23b ± 0.084 | 58.98b ± 3.06 | 73.13b ± 3.79 |
Thioacetamide (TAA; 100 mg/kg) | 129.13a ± 17.09 | 95.54a ± 3.53 | 1.20a ± 0.249 | 126.53a ± 6.56 | 156.90a ± 8.14 |
TAA + crocin 25 mg/kg | 52.86a,b ± 0.43 | 47.28a,b ± 3.22 | 0.83a,b ± 0.29 | 124.00a ± 6.43 | 153.76a ± 7.97 |
TAA + crocin 100 mg/kg | 28.00a,b ± 0.50 | 29.14a,b ± 5.18 | 0.36a,b ± 0.129 | 69.45a,b ± 3.60 | 86.12a,b ± 4.46 |
TAA + silymarin100 mg/kg | 22.17b ± 5.24 | 19.46b ± 4.32 | 0.29b ± 0.103 | 64.29b ± 3.33 | 79.71b ± 4.13 |
n = 6.
Statistical analysis was carried out by a one-way ANOVA followed by Tukey’s post hoc test.
Statistically significant from the corresponding control at p < 0.05.
Statistically significant from TAA-treated group at p < 0.05.