Omote M, Sakai K, Mizusawa H
Marion Merrell Dow, Osaka, Japan.
Arzneimittelforschung. 1994 Feb;44(2):149-53.
The acute effects of deflazacort (MDL 458, CAS 14484-47-0) and its metabolite, 21-desacetyl-deflazacort, on allergic reactions in animal models were investigated and compared with those of prednisolone. Deflazacort, 21-desacetyl-deflazacort and prednisolone all inhibited 48-h homologous passive cutaneous anaphylaxis in rats, but had no significant effects on active systemic anaphylaxis in mice, on the Schultz-Dale reaction in the isolated guinea-pig trachea or on compound 48/80-induced histamine release in rat peritoneal mast cells. All three agents inhibited reversed cutaneous anaphylaxis in rats and the Arthus reaction in mice. The inhibitory effects of deflazacort on the passive cutaneous anaphylaxis, the reversed cutaneous anaphylaxis and the Arthus reaction were similar to those of 21-desacetyl-deflazacort and were stronger than those of prednisolone. Delayed type hypersensitivity in mice was also inhibited by deflazacort and 21-desacetyl-deflazacort, but prednisolone, at the doses used in the present study, had little effect on this immune response. These findings indicate that while deflazacort and 21-desacetyl-deflazacort have stronger anti-allergic effects than prednisolone, they seem to have little acute effect on mast cell degranulation or on chemical mediators at the receptor site.
研究了去氟可特(MDL 458,CAS 14484-47-0)及其代谢物21-去乙酰基去氟可特对动物模型过敏反应的急性影响,并与泼尼松龙进行了比较。去氟可特、21-去乙酰基去氟可特和泼尼松龙均能抑制大鼠48小时同源被动皮肤过敏反应,但对小鼠的主动全身过敏反应、离体豚鼠气管的舒尔茨-戴尔反应或大鼠腹腔肥大细胞中化合物48/80诱导的组胺释放均无显著影响。这三种药物均能抑制大鼠的反向皮肤过敏反应和小鼠的阿瑟斯反应。去氟可特对被动皮肤过敏反应、反向皮肤过敏反应和阿瑟斯反应的抑制作用与21-去乙酰基去氟可特相似,且强于泼尼松龙。去氟可特和21-去乙酰基去氟可特也能抑制小鼠的迟发型超敏反应,但在本研究中使用的剂量下,泼尼松龙对这种免疫反应几乎没有影响。这些发现表明,虽然去氟可特和21-去乙酰基去氟可特的抗过敏作用比泼尼松龙更强,但它们似乎对肥大细胞脱颗粒或受体部位的化学介质几乎没有急性影响。