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©2007 Baishideng Publishing Group Co.
World J Gastroenterol. Aug 28, 2007; 13(32): 4328-4332
Published online Aug 28, 2007. doi: 10.3748/wjg.v13.i32.4328
Published online Aug 28, 2007. doi: 10.3748/wjg.v13.i32.4328
Figure 1 Histologic appearance of representative livers for cystamine treatment and fibrosis control rats.
A, B: Cystamine treatment ameliorated liver damage (A × 100, B × 200); C, D: Fibrosis control livers from CCl4-treated rats showed substantial damage including inflammation, fine fibrils and degeneration of hepatocytes (C × 100, D × 200).
Figure 2 Hepatic function changes of each group.
A: the level of ALT after Cystamine treatment; B: the level of TB after Cystamine treatment; C: the level of TBA after Cystamine treatment. bP < 0.01 vs Control; dP < 0.01 vs Fibrosis.
Figure 3 Difference of mRNA expression in each group.
A: relative expression of tTG after Cystamine treatment; B: relative expression of a-SMA after Cystamine treatment; C: relative expression of Collagen-1 after Cystamine treatment; D: relative expression of TIMP-1 after Cystamine treatment. bP < 0.01 vs Control; dP < 0.01 vs Fibrosis.
Figure 4 Different level of tTG protein in each group.
tTG relative expression after Cystamine treatment. bP < 0.01 vs Control; dP < 0.01 vs Fibrosis.
Figure 5 Different level of α-SMA protein in each group.
α-SMA relative expression after Cystamine treatment. bP < 0.01 vs Control; dP < 0.01 vs Fibrosis.
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Citation: Qiu JF, Zhang ZQ, Chen W, Wu ZY. Cystamine ameliorates liver fibrosis induced by carbon tetrachloride
via inhibition of tissue transglutaminase. World J Gastroenterol 2007; 13(32): 4328-4332 - URL: https://www.wjgnet.com/1007-9327/full/v13/i32/4328.htm
- DOI: https://dx.doi.org/10.3748/wjg.v13.i32.4328