Tsuji F, Miyake Y, Horiuchi M, Mita S
Discovery Research Division, Santen Pharmaceutical Co., Ltd., Osaka, Japan.
Biochem Pharmacol. 1998 Feb 1;55(3):297-304. doi: 10.1016/s0006-2952(97)00464-4.
Leukotriene B4 (LTB4) is a product of the 5-lipoxygenase pathway of arachidonic acid (AA) metabolism. LTB4 is a potent chemotactic factor for neutrophils and has been postulated to play an important role in a variety of pathological conditions including rheumatoid arthritis, psoriasis, and inflammatory bowel disease. To investigate the role of LTB4 in dermatitis, we used S-(4-dimethylaminobenzyl)-N-[(2S)-3-mercapto-2-methylpropionyl]-L- cysteine (SA6541), a potent leukotriene A4 (LTA4) hydrolase inhibitor. SA6541 inhibited LTB4 production with an IC50 value of 270 nM in vitro. 5-Hydroperoxyeicosatetraenoic acid (5-HPETE) or AA injection induced LTB4 production and neutrophil influx in mouse ear. SA6541 inhibited 5-HPETE- and AA-induced LTB4 production and neutrophil influx in mouse ear when administered orally at a dose of 50 mg/kg. SA6541 also inhibited 5-HPETE-induced prostaglandin E2 (PGE2) production, probably by an indirect effect through the inhibition of LTB4 production. These results suggest that LTB4 may be important in the pathogenesis of dermatitides such as psoriasis.
白三烯B4(LTB4)是花生四烯酸(AA)代谢的5-脂氧合酶途径的产物。LTB4是一种对中性粒细胞有强大趋化作用的因子,据推测在包括类风湿性关节炎、银屑病和炎症性肠病在内的多种病理状况中发挥重要作用。为了研究LTB4在皮炎中的作用,我们使用了S-(4-二甲基氨基苄基)-N-[(2S)-3-巯基-2-甲基丙酰基]-L-半胱氨酸(SA6541),一种有效的白三烯A4(LTA4)水解酶抑制剂。SA6541在体外以270 nM的IC50值抑制LTB4的产生。5-氢过氧化二十碳四烯酸(5-HPETE)或AA注射可诱导小鼠耳部LTB4的产生和中性粒细胞流入。当以50 mg/kg的剂量口服给药时,SA6541可抑制5-HPETE和AA诱导的小鼠耳部LTB4的产生和中性粒细胞流入。SA6541还可能通过抑制LTB4的产生产生间接作用,从而抑制5-HPETE诱导的前列腺素E2(PGE2)的产生。这些结果表明,LTB4可能在银屑病等皮炎的发病机制中起重要作用。