Escrig V, Ubeda A, Ferrandiz M L, Darias J, Sanchez J M, Alcaraz M J, Paya M
Department of Pharmacology, University of Valencia and Institute of Natural Products and Agrobiology, Tenerife, Spain.
J Pharmacol Exp Ther. 1997 Jul;282(1):123-31.
The marine product variabilin was identified as a novel inhibitor of phospholipase A2 (PLA2), which exhibited IC50 values of 6.9 microM and 7.9 microM for human synovial secretory PLA2 and U937 cells cytosolic PLA2 activities, respectively. This compound was less potent on bee venom or zymosan-injected rat air pouch enzymes and failed to affect Naja naja venom PLA2. The production of leukotriene B4 by human neutrophils stimulated with calcium ionophore A23187 was also inhibited by variabilin, which was without effect on 5-lipoxygenase, cyclo-oxygenase 1 and cyclo-oxygenase 2 activities in cell-free assays. Other functions of human neutrophils, such as degranulation and superoxide generation, were also significantly reduced in vitro. Variabilin administered topically suppressed the mouse ear edema induced by 12-O-tetradecanoylphorbol 13-acetate, whereas the ear edema induced by arachidonic acid was unaffected; this suggests an action previous to arachidonic acid metabolism. This compound administered p.o. at 30 mg/kg and 45 mg/kg significantly inhibited mouse paw edema induced by carrageenan and, at 0.01 to 1.0 micromol/pouch in the mouse air pouch injected with zymosan, exerted a marked inhibition on PGE2 and leukotriene B4 levels in exudates (ID50 values of approximately 0.028-0.029 micromol/pouch), without affecting cell migration. Our results indicate that variabilin is an inhibitor of human secretory and cytosolic PLA2 activities that controls eicosanoid production in vitro and in vivo, inhibits neutrophil degranulation and superoxide generation in vitro and shows anti-inflammatory activity after topical or p.o. administration to mice.
海洋产物变豆菜素被鉴定为磷脂酶A2(PLA2)的一种新型抑制剂,它对人滑膜分泌型PLA2和U937细胞胞质型PLA2活性的IC50值分别为6.9微摩尔和7.9微摩尔。该化合物对蜂毒或酵母聚糖注射的大鼠气囊酶的抑制作用较弱,且对眼镜蛇毒PLA2无影响。变豆菜素还能抑制钙离子载体A23187刺激的人中性粒细胞产生白三烯B4,在无细胞试验中,它对5-脂氧合酶、环氧化酶1和环氧化酶2的活性没有影响。人中性粒细胞的其他功能,如脱颗粒和超氧化物生成,在体外也显著降低。局部应用变豆菜素可抑制12-O-十四烷酰佛波醇-13-乙酸酯诱导的小鼠耳部水肿,而花生四烯酸诱导的耳部水肿则不受影响;这表明其作用发生在花生四烯酸代谢之前。该化合物以30毫克/千克和45毫克/千克的剂量口服,可显著抑制角叉菜胶诱导的小鼠爪部水肿,在向注射酵母聚糖的小鼠气囊中注射0.01至1.0微摩尔/气囊时,对渗出液中PGE2和白三烯B4水平有显著抑制作用(ID50值约为0.028 - 0.029微摩尔/气囊),且不影响细胞迁移。我们的结果表明,变豆菜素是一种人分泌型和胞质型PLA2活性的抑制剂,在体外和体内均可控制类花生酸的产生,在体外抑制中性粒细胞脱颗粒和超氧化物生成,并在局部或口服给药后对小鼠显示出抗炎活性。