Saito H, Yamamoto N, Tomita S, Taniguchi M, Hasegawa M, Akiyama K, Kawaguchi H, Takahashi K
Clinical Research Center for Rheumatology and Allergy, National Sagamihara Hospital, Sagamihara, Japan.
Int Arch Allergy Immunol. 2001;125 Suppl 1:22-8. doi: 10.1159/000053848.
Emedastine difumarate (emedastine) is an antiallergic drug found among the derivatives which has a series of benzimidazole frames. It has been reported that emedastine can significantly inhibit the migration of eosinophils elicited by classical chemoattractants, including LTB4 or PAF. However, the effect of emedastine on the selective migration of eosinophils that have been stimulated with CC chemokines has not been examined. Emedastine at concentrations of 10 nM or higher strongly inhibited the eosinophil migration elicited by CC chemokines, including eotaxin, RANTES and MCP-3. Preincubation of the eosinophils with emedastine did not alter the expression of the CCR3 receptor, although a decrease in the concentration of intracellular calcium ions was observed after stimulation with 100 ng/ml of eotaxin. Herbimycin A, genistein, staurosporin and emedastine were all able to inhibit the eotaxin-elicited migration. Tyrosine kinase activity in the cytosol supernatant of eosinophils obtained after stimulation with eotaxin significantly decreased when the eosinophils were preincubated with emedastine. In addition, protein kinase A and protein kinase C activities in eotaxin-stimulated EoL-1 cell supernatants decreased significantly with emedastine pretreatment. These findings suggest that emedastine inhibits CC chemokine-elicited eosinophil migration by decreasing the activities of tyrosine kinase or protein kinases but does not alter CCR3 expression.
富马酸依美斯汀(依美斯汀)是一种存在于具有一系列苯并咪唑骨架的衍生物中的抗过敏药物。据报道,依美斯汀可显著抑制由经典趋化因子(包括白三烯B4或血小板活化因子)引发的嗜酸性粒细胞迁移。然而,依美斯汀对经CC趋化因子刺激的嗜酸性粒细胞选择性迁移的影响尚未得到研究。浓度为10 nM或更高的依美斯汀强烈抑制由CC趋化因子(包括嗜酸性粒细胞趋化因子、调节活化正常T细胞表达和分泌的趋化因子及单核细胞趋化蛋白-3)引发的嗜酸性粒细胞迁移。用依美斯汀对嗜酸性粒细胞进行预孵育不会改变CCR3受体的表达,尽管在用100 ng/ml嗜酸性粒细胞趋化因子刺激后观察到细胞内钙离子浓度降低。赫曲霉素A、染料木黄酮、星形孢菌素和依美斯汀均能够抑制嗜酸性粒细胞趋化因子引发的迁移。当嗜酸性粒细胞用依美斯汀预孵育后,经嗜酸性粒细胞趋化因子刺激后获得的嗜酸性粒细胞胞质上清液中的酪氨酸激酶活性显著降低。此外,经依美斯汀预处理后,嗜酸性粒细胞趋化因子刺激的EoL-1细胞上清液中的蛋白激酶A和蛋白激酶C活性显著降低。这些发现表明,依美斯汀通过降低酪氨酸激酶或蛋白激酶的活性来抑制CC趋化因子引发的嗜酸性粒细胞迁移,但不会改变CCR3的表达。