Baker J R, Selden L F
Trans R Soc Trop Med Hyg. 1981;75(1):80-5. doi: 10.1016/0035-9203(81)90015-8.
Cultivated trypomastigotes of Trypanosoma (Schizotrypanum) dionisii were added to cultures of buffalo lung (BL) cells at 37 degrees C in a ratio of 500 parasites per cell. More than 60% of the cells became infected with amastigotes and the system was used to test trypanosomicidal activity and cytotoxicity of possible chemotherapeutic agents for use in Chagas's disease. Three nitroheterocyclic compounds known to be active against T. cruzi in cell cultures (nifurtimox, benznidazole and SQ 18506) were active at similar levels against intracellular T. dionisii (1, 10 and 0.1 microgram ml-1 respectively); concentrations of 10, 10 and 1 microgram ml-1 respectively were cytotoxic. Other substances, not regarded as active against T. cruzi (metronidazole, pentamidine and pentostam, had little or no trypanosomicidal effect even at 100 microgram ml-1. A recently developed nitroheterocyclic compound (MK 436) was active, and not cytotoxic, at 10 microgram ml-1 and possibly warrants further investigation Tetraethylthiuram disulphide, an inhibitor of threonine dehydrogenase which prevents growth of extracellular T. cruzi and T. dionisii in vitro at 1 microgram ml-1, was only slightly trypanosomicidal to intracellular T. dionisii at this dose; it was also somewhat cytotoxic.
将培养的克氏锥虫(裂殖锥虫属)杜氏锥虫无鞭毛体以每细胞500个寄生虫的比例添加到37摄氏度的水牛肺(BL)细胞培养物中。超过60%的细胞被无鞭毛体感染,该系统用于测试用于恰加斯病的可能化疗药物的杀锥虫活性和细胞毒性。已知在细胞培养中对克氏锥虫有活性的三种硝基杂环化合物(硝呋莫司、苯硝唑和SQ 18506)对细胞内杜氏锥虫的活性水平相似(分别为1、10和0.1微克/毫升);浓度分别为10、10和1微克/毫升时具有细胞毒性。其他不被认为对克氏锥虫有活性的物质(甲硝唑、喷他脒和戊烷脒)即使在100微克/毫升时也几乎没有或没有杀锥虫作用。一种最近开发的硝基杂环化合物(MK 436)在10微克/毫升时具有活性且无细胞毒性,可能值得进一步研究。二硫化四乙秋兰姆,一种苏氨酸脱氢酶抑制剂,在1微克/毫升时可阻止细胞外克氏锥虫和杜氏锥虫在体外生长,在该剂量下对细胞内杜氏锥虫只有轻微的杀锥虫作用;它也有一定的细胞毒性。