2009
DOI: 10.1007/s00535-008-2267-5
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Mast cells are involved in the pathogenesis of indomethacin-induced rat enteritis

Abstract: These results indicate that mast cells are involved in the pathogenesis of the intestinal mucosal damage induced by indomethacin.

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Cited by 10 publications
(3 citation statements)
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“…Gnotobiotic rats mono-associated with Bifidobacterium or Lactobacillus have no ulcers after NSAID administration, while mono-association with Escherichia coli or Eubacterium limosum induces ileal ulcer formation [71]. On the other hand, the development of intestinal lesions in response to indomethacin is prevented in mast cell-deficient rats [72]. It has been shown that orally administered GMP induces an increment in the amount of Lactobacillus and Bifidobacteria in the fecal microbiota of mice [73], and that this bioactive peptide avoids the adhesion of enterohemorrhagic E. coli O157:H7 on Caco-2 cells [74].…”
Section: Discussionmentioning
confidence: 99%
“…Gnotobiotic rats mono-associated with Bifidobacterium or Lactobacillus have no ulcers after NSAID administration, while mono-association with Escherichia coli or Eubacterium limosum induces ileal ulcer formation [71]. On the other hand, the development of intestinal lesions in response to indomethacin is prevented in mast cell-deficient rats [72]. It has been shown that orally administered GMP induces an increment in the amount of Lactobacillus and Bifidobacteria in the fecal microbiota of mice [73], and that this bioactive peptide avoids the adhesion of enterohemorrhagic E. coli O157:H7 on Caco-2 cells [74].…”
Section: Discussionmentioning
confidence: 99%
“…Indomethacin-induced gastric ulcer by inhibition of prostaglandins which are cytoprotective to gastric mucosa [11]. Moreover, it was reported that indomethacin causes significant gastrointestinal damage [12] and several enteropathic consequences, including oxidative stress [13].…”
Section: Introductionmentioning
confidence: 99%
“…According to Okayama’ method of modeling with some modifies [ 16 ], 32 Rats were equally and randomly divided into 4 groups: Control group, indomethacin group, PGP (0.253 g/kg) group, PGP (0.759 g/kg) group. After being adaptively fed for 5 days, the model of intestinal mucosal injury was replicated and administered.…”
Section: Methodsmentioning
confidence: 99%