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5-Aminosalicylic Acid Inhibits AcuteClostridium difficileToxin A-Induced Colitis in Rats
Author(s) -
Steven R. Vigna
Publication year - 2014
Publication title -
international journal of inflammation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.106
H-Index - 33
eISSN - 2090-8040
pISSN - 2042-0099
DOI - 10.1155/2014/389621
Subject(s) - sulfasalazine , sulfapyridine , toxin , colitis , leukotriene b4 , clostridium difficile toxin a , pharmacology , medicine , aminosalicylic acid , inflammation , capsaicin , microbiology and biotechnology , chemistry , antibiotics , biology , clostridium difficile , ulcerative colitis , receptor , disease , organic chemistry
We tested the hypothesis that 5-aminosalicylic acid (5-ASA) inhibits toxin A-induced generation of colonic leukotriene B 4 (LTB 4 ) and toxin A colitis in rats. Isolated colonic segments in anesthetized rats were treated intraluminally with toxin A for 3 hours with or without 30 minutes of pretreatment with either 5-ASA or sulfapyridine and then colonic tissue levels of LTB 4 were measured and inflammation was assessed. Separately, sulfasalazine was administered to rats in their drinking water for 5 days, isolated colonic segments were then prepared, toxin A was administered, and inflammation was assessed as before. Pretreatment with 5-ASA inhibited toxin A-induced increased tissue LTB 4 concentration in the colon. Sulfasalazine and 5-ASA but not sulfapyridine significantly inhibited toxin A colitis. However, pretreatment with 5-ASA did not protect against direct TRPV1-mediated colitis caused by capsaicin. Toxin A stimulated the release of substance P (SP), and this effect was also inhibited by sulfasalazine and 5-ASA but not by sulfapyridine. Thus, toxin A stimulates colonic LTB 4 resulting in activation of TRPV1, release of SP, and colitis. Inhibition of 5-LO by 5-ASA disrupts this pathway and supports the concept that LTB 4 activation of TRPV1 plays a role in toxin A colitis.

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