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©2014 Baishideng Publishing Group Co.
World J Gastroenterol. Mar 14, 2014; 20(10): 2641-2652
Published online Mar 14, 2014. doi: 10.3748/wjg.v20.i10.2641
Published online Mar 14, 2014. doi: 10.3748/wjg.v20.i10.2641
Figure 5 Effects of drugs on indomethacin-induced vascular permeability and oxidative stress.
Animals were given indomethacin (10 mg/kg, po) and killed 24 h later. AL-Na (250 and 500 mg/kg) or Reb (100 mg/kg) was given orally twice at 30 min before and 6 h after administration of indomethacin. A Vascular permeability; B: Superdismdeoxidase content; C: Glutathione peroxidase activity; D: Catalase activity were measured. Each column and vertical bar represents the mean ± SE (n = 8). Significantly different from the control group at aP < 0.05 and bP < 0.01 (Student’s t-test); Significantly different from the indomethacin group at cP < 0.05 and dP < 0.01, respectively (Dunnett’s test). Cont: Control; IND: Indomethacin; AL-Na: Sodium alginate; Reb: Rebamipide.
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Citation: Yamamoto A, Itoh T, Nasu R, Nishida R. Sodium alginate ameliorates indomethacin-induced gastrointestinal mucosal injury
via inhibiting translocation in rats. World J Gastroenterol 2014; 20(10): 2641-2652 - URL: https://www.wjgnet.com/1007-9327/full/v20/i10/2641.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i10.2641