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.
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Authors | N Clapp, M Henke, R Hansard, R Carson, R Walsh, D Widomski, C Anglin, D Fretland |
Journal | Agents and actions
(Agents Actions)
Vol. 39 Spec No
Pg. C8-10
( 1993)
ISSN: 0065-4299 [Print] Switzerland |
PMID | 8273593
(Publication Type: Journal Article)
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Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Arachidonic Acids
- Benzopyrans
- Platelet Activating Factor
- SC 41930
- Leukotriene B4
- Thromboxane B2
- Dinoprostone
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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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