el-On J, Rubinstein N, Kernbaum S, Schnur L F
Ann Trop Med Parasitol. 1986 Oct;80(5):509-17. doi: 10.1080/00034983.1986.11812057.
Chlorpromazine (CPZ) was effective in vitro against leishmanial promastigotes and amastigotes. CPZ at 7.5 micrograms ml-1 killed the promastigotes of Leishmania mexicana, L. aethiopica and L. major within 24 hours of exposure. A higher concentration was required to achieve the same effect against L. donovani. N-meglumine antimonate (MGA) was only partially effective against the promastigotes of the four strains studied. Even at 1000 micrograms ml-1 total destruction of the parasites did not occur within four days of treatment. Combination chemotherapy of CPZ and MGA generally showed an additive effect against promastigotes. However, a synergistic effect was observed in the case of L. donovani promastigotes and L. major amastigotes in vitro. No significant effect was obtained against the amastigotes of L. major and L. mexicana in vivo, in cutaneous lesions of BALB/c mice.
氯丙嗪(CPZ)在体外对利什曼原虫前鞭毛体和无鞭毛体有效。浓度为7.5微克/毫升的CPZ在暴露24小时内可杀死墨西哥利什曼原虫、埃塞俄比亚利什曼原虫和硕大利什曼原虫的前鞭毛体。对杜氏利什曼原虫达到相同效果则需要更高的浓度。葡甲胺锑酸盐(MGA)仅对所研究的四种菌株的前鞭毛体有部分效果。即使在1000微克/毫升的浓度下,处理四天内也未实现寄生虫的完全杀灭。CPZ和MGA联合化疗通常对前鞭毛体显示出相加作用。然而,在体外观察到杜氏利什曼原虫前鞭毛体和硕大利什曼原虫无鞭毛体有协同作用。在BALB/c小鼠的皮肤病变中,对硕大利什曼原虫和墨西哥利什曼原虫的无鞭毛体在体内未获得显著效果。