Leukotriene B4Plays a Critical Role in the Progression of Collagen- Induced Arthritis

Leukotriene B4(LTB4) is a product of the 5-lipoxygenase pathway of arachidonic acid metabolism. LTB4is a potent chemotactic factor for neutrophils and has been postulated to play an important role in a variety of pathological conditions including rheumatoid arthritis (RA), psoriasis, and inflammator...

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Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 1995-01, Vol.92 (2), p.517-521
Main Authors: Griffiths, R. J., Pettipher, E. R., Koch, K., Farrell, C. A., Breslow, R., Conklyn, M. J., Smith, M. A., Hackman, B. C., Wimberly, D. J., Milici, A. J., Scampoli, D. N., Cheng, J. B., Pillar, J. S., Pazoles, C. J., Doherty, N. S., Melvin, L. S., Reiter, L. A., Biggars, M. S., Falkner, F. C., Mitchell, D. Y., Liston, T. E., Showell, H. J.
Format: Article
Language:English
Subjects:
Arthritis
Body weight
Chemotaxis
Collagens
Disease models
Dosage
Joint diseases
Mice
Neutrophils
Receptors
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Summary:Leukotriene B4(LTB4) is a product of the 5-lipoxygenase pathway of arachidonic acid metabolism. LTB4is a potent chemotactic factor for neutrophils and has been postulated to play an important role in a variety of pathological conditions including rheumatoid arthritis (RA), psoriasis, and inflammatory bowel disease. The role of LTB4in such diseases has not yet been defined but in this paper we provide direct evidence that LTB_4 plays a critical role in a murine model of RA. CP-105,696, (+)-1-(3S,4R)-[3-(4-phenylbenzyl)-4-hydroxychroman-7-yl]cyclopentane carboxylic acid, is an LTB4receptor antagonist that inhibits LTB_4 binding to human neutrophil membranes with an IC50of 3.7 nM and inhibits LTB4-induced chemotaxis of these cells with an IC50of 5.2 nM. CP-105,696 inhibits LTB4-induced neutrophil influx in mouse skin when administered orally with an ED50of 4.2 mg/kg. CP-105,696 had a dramatic effect on both the clinical symptoms and histological changes of murine collagen-induced arthritis when administered at doses of 0.3-10 mg/kg. Inhibition was not associated with suppression of the humoral immune response to collagen and was equally effective if drug treatment was commenced just prior to the onset of arthritis or throughout the experiment. These results suggest that LTB_4 receptor antagonists may be effective therapeutic agents for the treatment of RA.
ISSN:0027-8424