Copyright
©The Author(s) 2021.
World J Gastroenterol. Oct 28, 2021; 27(40): 6888-6907
Published online Oct 28, 2021. doi: 10.3748/wjg.v27.i40.6888
Published online Oct 28, 2021. doi: 10.3748/wjg.v27.i40.6888
Figure 1 Histological changes in various groups of rats.
HE staining, magnification: 400 ×. A: Normal control group; B: Model control group; C: Fuzi-Gancao (F-G) group (15 g/kg); D: F-G group (30 g/kg); E: Positive control group (silybin).
Figure 2 Serum metabolites in rats.
A: Partial Least-Squares Discriminant Analysis; B: P-test analysis. M: Model control group; N: Negative control group; F-G: Fuzi-Gancao group.
Figure 3 Metabolic pathway analysis of serum in rats.
A: Negative control group vs model control group; B: Fuzi-Gancao group vs model control group.
Figure 4 Bile acids in rats (n = 6, mean ± SD).
aP < 0.05, bP < 0.01 for each treatment group and model control group, respectively; cP < 0.05, dP < 0.01 for the model control group and normal control group, respectively.
Figure 5 Bile acids in rats.
A: Partial Least-Squares Discriminant Analysis; B: P-test analysis.
- Citation: Wang MF, Zhao SS, Thapa DM, Song YL, Xiang Z. Metabolomics of Fuzi-Gancao in CCl4 induced acute liver injury and its regulatory effect on bile acid profile in rats. World J Gastroenterol 2021; 27(40): 6888-6907
- URL: https://www.wjgnet.com/1007-9327/full/v27/i40/6888.htm
- DOI: https://dx.doi.org/10.3748/wjg.v27.i40.6888