In Vitro And In Vivo Pharmacological Characterization Of Sb 201993, An Eicosanoid-Like Ltb4 Receptor Antagonist With Anti-Inflammatory Activity

Hm Sarau,Jj Foley,Db Schmidt,Ld Martin,Ef Webb, Mn Tzimas,Jj Breton, M Chabot-Fletcher,Dc Underwood, Dwp Hay,Wd Kingsbury,Pa Chambers, I Pendrak,Dr Jakas,Gm Sathe, S Van Horn, Ra Daines,De Griswold

PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS(1999)

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摘要
Leukotriene B-4 (LTB4) and 12-(R)-hydroxy-5,8,10,14-eicosatetraenoic acid (12-[R]-HETE) have been postulated to contribute to the pathophysiology of inflammatory diseases. SE 201993, (E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl] oxy]-2-pyridinyl] methyl] thio] methyl] benzoic acid, identified from a chemical series designed as ring-fused analogs of LTB4, was evaluated as an antagonist of LTB4- and 12-(R)-HETE-induced responses in vitro and for anti-inflammatory activity in vivo. SE 201993 competitively antagonized [(3)-H]-LTB4 binding to intact human neutrophils (K-i = 7.6 nM) and to membranes of RBL 2H3 cells expressing the LTB4 receptor (RBL 2H3-LTB4R; IC50 = 154 nM). This compound demonstrated competitive antagonism of LTB4- and 12-(R)-HETE-induced Ca2+ mobilization responses in human neutrophils (IC(50)s of 131 nM and 105 nM, respectively) and inhibited LTB4-induced Ca2+ mobilization in human cultured keratinocytes (IC50 = 61 nM), RBL 2H3-LTB4R cells (IC50 = 255 nM) and mouse neutrophils (IC50 = 410 nM). SE 201993 showed weak LTD4-receptor binding affinity (K-i = 1.9 mu M) and inhibited 5-lipoxygenase (IC50 of 3.6 mu M), both in vitro and ex vivo. In vivo, SE 201993 inhibited LTB4-induced neutrophil infiltration in mouse skin and produced dose-related, long lasting topical anti-inflammatory activity against the fluid and cellular phases of arachidonic acid-induced mouse ear inflammation (ED50 of 580 mu g/ear and 390 mu g/ear, respectively). Similarly, anti-inflammatory activity was also observed in the murine phorbol ester-induced cutaneous inflammation model (ED50 of 770 and 730 mu g/ear, respectively, against the fluid and cellular phases). These results indicate that SE 201993 blocks the actions of LTB4 and 12-(R)-HETE and inhibits a variety of inflammatory responses; and thus may be a useful compound to evaluate the role of these mediators in disease models.
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