Williamson J, McLaren D J, Brown J R
Cell Biol Int Rep. 1983 Dec;7(12):997-1005. doi: 10.1016/0309-1651(83)90004-8.
The nucleus (but not the kinetoplast) of Trypanosoma rhodesiense is the principal target for trypanocidal attack by Daunomycin in vitro and Daunomycin-protein conjugates in vivo; free Daunomycin is inactive in vivo. Nucleolar segregation and abnormal distribution of heterochromatin occur after drug treatment as in tumour cells. Other abnormal changes include formation of cytoplasmic clefts and autophagic vacuoles, increased prominence of the tubular collection system, and exocytotic vesicle production. Large masses of ferritin accumulate in white cells after treatment with the drug-ferritin conjugate but no ferritin was detectable in trypanosomes.
罗德西亚锥虫的细胞核(而非动基体)是体外阿霉素和体内阿霉素 - 蛋白质缀合物杀锥虫攻击的主要靶点;游离阿霉素在体内无活性。药物处理后会出现核仁分离和异染色质异常分布,如同在肿瘤细胞中一样。其他异常变化包括细胞质裂隙和自噬泡的形成、管状收集系统的突出增加以及胞吐小泡的产生。用药物 - 铁蛋白缀合物处理后,白细胞中会积累大量铁蛋白,但在锥虫中未检测到铁蛋白。