Zweygarth E, Röttcher D
Chemotherapy of Trypanosomiasis Research Project, Deutsche Gesellschaft für Technische Zusammenarbeit, Kabete, Kenya.
Parasitol Res. 1989;75(3):178-82. doi: 10.1007/BF00931271.
Several experimental trypanocidal compounds, 6-amidino-2-(4-amidinophenyl)indole dilactate (DAPI), DL-alpha-difluoromethylornithine (DFMO), 2-(dimethylamino)-4'-[(1-methyl-2-nitroimidazole-5-yl) methoxy] aceto-anilide (Ro 15-0216), sinefungin, and triacetylbenzene-tris(guanylhydrazone)trimethanesulfonate hydrate (TBG-MS) were tested to evaluate their ability to cure mouse infections with a multiple drug-resistant Trypanosoma brucei brucei stock (CP 547). This stock proved to be drug-resistant against diminazene aceturate, homidium chloride, isometamidium, quinapyramine sulfate, Mel B, and pentamidine isethionate but fully sensitive to suramin. Compared with the sensitive stock CP 462, the drug-resistant stock CP 547 was completely resistant to 16-fold the curative dose of sinefungin and partially resistant to 4-fold the curative dose of DAPI and to 13-fold the curative dose of TBG-MS, a dose that killed 25% of the animals due to its toxicity. Ro 15-0216 cured all mice when 18 times the usual curative dose level was given. DFMO was equally effective against both stocks.
对几种实验性杀锥虫化合物进行了测试,包括6-脒基-2-(4-脒基苯基)吲哚二乳酸盐(DAPI)、DL-α-二氟甲基鸟氨酸(DFMO)、2-(二甲氨基)-4'-[(1-甲基-2-硝基咪唑-5-基)甲氧基]乙酰苯胺(Ro 15-0216)、杀稻瘟菌素以及三乙酰苯三(胍基腙)三甲基磺酸盐一水合物(TBG-MS),以评估它们治愈小鼠多重耐药布氏布氏锥虫(CP 547株)感染的能力。该毒株对乙酰氨基阿苯达唑、氯化血根碱、异美汀、硫酸喹啉脲、美拉胂醇B和乙磺半胱氨酸戊烷脒耐药,但对苏拉明完全敏感。与敏感株CP 462相比,耐药株CP 547对杀稻瘟菌素治疗剂量的16倍完全耐药,对DAPI治疗剂量的4倍部分耐药,对TBG-MS治疗剂量的13倍部分耐药,该剂量因毒性导致25%的动物死亡。当给予18倍常规治疗剂量水平时,Ro 15-0216治愈了所有小鼠。DFMO对这两种毒株同样有效。