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©2010 Baishideng.
World J Gastroenterol. Jun 21, 2010; 16(23): 2873-2880
Published online Jun 21, 2010. doi: 10.3748/wjg.v16.i23.2873
Published online Jun 21, 2010. doi: 10.3748/wjg.v16.i23.2873
Figure 2 Effects of CXCR4 antagonist on colonic myeloperoxidase (MPO), proinflammatory cytokines, and gut permeability in mice.
Colitis was induced by administration of 5% DSS for 7 d. Colonic levels of tumor necrosis factor-α (TNF-α) (A), interleukin-6 (IL-6) (B), interferon-γ (IFN-γ) (C), MPO (D), and FD4 clearance (E) are shown. Eight mice were studied in each experimental group. Results are mean ± SE. aP < 0.05 vs control group; cP < 0.05 vs DSS + PBS group.
- Citation: Xia XM, Wang FY, Xu WA, Wang ZK, Liu J, Lu YK, Jin XX, Lu H, Shen YZ. CXCR4 antagonist AMD3100 attenuates colonic damage in mice with experimental colitis. World J Gastroenterol 2010; 16(23): 2873-2880
- URL: https://www.wjgnet.com/1007-9327/full/v16/i23/2873.htm
- DOI: https://dx.doi.org/10.3748/wjg.v16.i23.2873