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Inflammatory mediator changes in cotton-top tamarins (CTT) after SC-41930 anti-colitic therapy.

Abstract
Use of the CTT model provides insight into the inflammatory mediator contribution in the pathogenesis of idiopathic colitis. To evaluate anti-colitic efficacy, the leukotriene B4 receptor antagonist and anti-inflammatory agent, SC-41930, was administered (10 mg/kg BW by gavage BID) for 8 weeks to CTTs with histologically confirmed persistent and defined active colitis. The inflammatory mediators LTB4, PGE2, TXB2, and PAF were assayed in colonic dialysate that was collected after 1 1/2 h from four CTTs pre-, mid-, and post-treatment, frozen at -70 degrees C, and analyzed by RIA after HPLC purification. LTB4 levels were lower at mid- and post-treatment and had little inter-animal variation post-treatment. PGE2 and PAF levels were elevated during SC-41930 treatment, but there was a trend towards lower thromboxane B2 levels. Reduced LTB4 (PMN degranulation and chemotaxis) and increased PGE2 (mucosal-protective effect) may, in part, explain the observed efficacy of SC-41930 in active tamarin colitis.
AuthorsN Clapp, M Henke, R Hansard, R Carson, R Walsh, D Widomski, C Anglin, D Fretland
JournalAgents and actions (Agents Actions) Vol. 39 Spec No Pg. C8-10 ( 1993) ISSN: 0065-4299 [Print] Switzerland
PMID8273593 (Publication Type: Journal Article)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Arachidonic Acids
  • Benzopyrans
  • Platelet Activating Factor
  • SC 41930
  • Leukotriene B4
  • Thromboxane B2
  • Dinoprostone
Topics
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal (pharmacology)
  • Arachidonic Acids (metabolism)
  • Benzopyrans (administration & dosage, pharmacology, therapeutic use)
  • Colitis (drug therapy, metabolism)
  • Colon (metabolism)
  • Dinoprostone (metabolism)
  • Disease Models, Animal
  • Leukotriene B4 (antagonists & inhibitors, metabolism)
  • Platelet Activating Factor (metabolism)
  • Radioimmunoassay
  • Saguinus
  • Thromboxane B2 (metabolism)

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