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©The Author(s) 2024.
World J Hepatol. Sep 27, 2024; 16(9): 1278-1288
Published online Sep 27, 2024. doi: 10.4254/wjh.v16.i9.1278
Published online Sep 27, 2024. doi: 10.4254/wjh.v16.i9.1278
Figure 5 C23 inhibits transforming growth factor beta/Smad3 activation in the fibrotic pathway.
A: Heatmap of the transcriptome array comparing the expression of genes involved in the regulation of fibrosis function between carbon tetrachloride (CCl4)-treated and CCl4+C23-treated mouse livers harvested 30 days after the procedure, n = 3; B: Western blotting was used to examine changes in the expression of factors involved in the transforming growth factor beta (TGF-β)/Smad3 signaling pathway during liver fibrosis. β-Actin was used as an internal reference protein; C: The gray value was calculated for p-Smad-3/Smad-3; D: The gray value was calculated for TGF-β/β-actin. aP < 0.05, bP < 0.01 vs carbon tetrachloride. CCl4: Carbon tetrachloride; TGF-β: Transforming growth factor beta.
- Citation: Tang RX, Xie XJ, Xiong Y, Li S, Luo C, Wang YG. C23 ameliorates carbon tetrachloride-induced liver fibrosis in mice. World J Hepatol 2024; 16(9): 1278-1288
- URL: https://www.wjgnet.com/1948-5182/full/v16/i9/1278.htm
- DOI: https://dx.doi.org/10.4254/wjh.v16.i9.1278