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依巴斯汀(WAL 801 CL)对速发型超敏反应的抗过敏作用:(I).组胺释放抑制机制的阐明。

Antiallergic effect of epinastine (WAL 801 CL) on immediate hypersensitivity reactions: (I). Elucidation of the mechanism for histamine release inhibition.

作者信息

Kamei C, Akagi M, Mio M, Kitazumi K, Izushi K, Masaki S, Tasaka K

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.

出版信息

Immunopharmacol Immunotoxicol. 1992;14(1-2):191-205. doi: 10.3109/08923979209009219.

Abstract

Epinastine caused an inhibition of histamine release from rat peritoneal mast cells induced by both antigen-antibody reaction and compound 48/80. Epinastine was similarly effective in inhibiting compound 48/80-induced histamine release not only from isolated rat peritoneal mast cells but also from rat mesenterial pieces. Also, histamine release from lung pieces obtained from actively sensitized guinea pigs after exposure to antigen challenge was markedly inhibited by epinastine. The drug was effective in inhibiting not only Ca2+ uptake into lung mast cells in actively sensitized guinea pigs but also Ca2+ release from the intracellular Ca store of rat peritoneal mast cells exposed to both compound 48/80 and substance P. No significant changes were observed in phosphodiesterase activity in rat peritoneal mast cells treated with epinastine, while adenylate cyclase activity was augmented by epinastine. Epinastine has no inhibitory effect on histamine release induced by Ca2+ or IP3 from permeabilized mast cells. However, the drug significantly and dose-dependently suppressed calmodulin activity suggesting that histamine release inhibition due to epinastine may be partly attributable to Ca(2+)-calmodulin dependent process(es). The drug caused no visible changes in thermodynamic behavior of lipids, either in order parameter or in differential scanning calorimetry, indicating that the drug has no influence on membrane fluidity.

摘要

依匹斯汀可抑制抗原 - 抗体反应和化合物48/80诱导的大鼠腹腔肥大细胞组胺释放。依匹斯汀不仅对分离的大鼠腹腔肥大细胞,而且对大鼠肠系膜组织,在抑制化合物48/80诱导的组胺释放方面同样有效。此外,依匹斯汀还能显著抑制主动致敏豚鼠肺组织在抗原激发后组胺的释放。该药物不仅能抑制主动致敏豚鼠肺肥大细胞对Ca2+的摄取,还能抑制化合物48/80和P物质作用下大鼠腹腔肥大细胞胞内钙库的Ca2+释放。用依匹斯汀处理的大鼠腹腔肥大细胞中磷酸二酯酶活性未见明显变化,而腺苷酸环化酶活性则被依匹斯汀增强。依匹斯汀对通透化肥大细胞中Ca2+或IP3诱导的组胺释放无抑制作用。然而,该药物能显著且剂量依赖性地抑制钙调蛋白活性,提示依匹斯汀对组胺释放的抑制作用可能部分归因于Ca(2+)-钙调蛋白依赖性过程。该药物在有序参数或差示扫描量热法方面均未引起脂质热力学行为的明显变化,表明该药物对膜流动性无影响。

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