de Melo A L, Hermeto M V, Bicalho R S, Vargas A P, Favaretto F J, Pereira L H
Grupo Interdepartamental de Estudos sobre Esquistossomose/Departamento de Parasitologia, Universidade Federal de Minas Gerais, Belo Horizonte, Brasil.
Rev Inst Med Trop Sao Paulo. 1994 Jan-Feb;36(1):89-93. doi: 10.1590/s0036-46651994000100014.
Treatment with dexamethasone (DMS) in the early phases of the experimental Schistosoma mansoni infection causes an indirect effect on the cercaria-schistosomulum transformation process. This is observed when naive albino mice are treated with that drug (50 mg/Kg, subcutaneously) and infected intraperitoneally 01 hour later with about 500 S. mansoni cercariae (LE strain). An inhibition in the host cell adhesion to the larvae, with a simultaneous delay in the cercaria-schistosomulum transformation, is observed. This effect is probably due to a blockade of the neutrophil migration to the peritoneal cavity of mice, by an impairment of the release of chemotactic substances. Such delay probably favors the killing of S. mansoni larvae, still in the transformation process, by the vertebrate host defenses, as the complement system.
在曼氏血吸虫感染实验的早期阶段,用地塞米松(DMS)治疗会对尾蚴-童虫转化过程产生间接影响。当未感染的白化小鼠用该药物(50毫克/千克,皮下注射)治疗,1小时后腹腔内感染约500条曼氏血吸虫尾蚴(LE株)时,即可观察到这种情况。观察到宿主细胞与幼虫的黏附受到抑制,同时尾蚴-童虫转化延迟。这种效应可能是由于趋化物质释放受损,导致中性粒细胞向小鼠腹腔的迁移受阻。这种延迟可能有利于脊椎动物宿主防御系统(如补体系统)杀死仍处于转化过程中的曼氏血吸虫幼虫。