Robinson N, Kaur K, Emmett K, Iovannisci D M, Ullman B
J Biol Chem. 1984 Jun 25;259(12):7637-43.
Formycin B is cytotoxic toward Leishmania and is a potential chemotherapeutic agent for leishmaniasis. In order to determine the mechanism of action of formycin B, we have isolated and characterized clonal populations of formycin B-resistant Leishmania donovani. These formycin B-resistant clones are also cross-resistant to formycin A and allopurinol riboside-mediated growth inhibition. Incubation of the formycin B-resistant cells with [3H]formycin B indicates that, unlike wild type cells, the resistant populations cannot accumulate phosphorylated metabolites of exogenous [3H]formycin B. This is due to a defective transport system for formycin B in the resistant cells. However, wild type and mutant cells incorporate [3H]formycin A equally efficiently into [3H]formycin A-containing nucleotides and into RNA. These data suggest that formycin B cytotoxicity in Leishmania is not mediated by its incorporation as the adenosine analog into RNA. A plausible alternative hypothesis is proposed for the mechanism of action of the pyrazolo (4,3-d)pyrimidine C-nucleosides based upon depletion of an essential intracellular metabolite.
间型霉素B对利什曼原虫具有细胞毒性,是治疗利什曼病的一种潜在化疗药物。为了确定间型霉素B的作用机制,我们分离并鉴定了对间型霉素B耐药的杜氏利什曼原虫的克隆群体。这些对间型霉素B耐药的克隆对间型霉素A和别嘌呤醇核糖苷介导的生长抑制也具有交叉耐药性。用[3H]间型霉素B孵育对间型霉素B耐药的细胞表明,与野生型细胞不同,耐药群体不能积累外源性[3H]间型霉素B的磷酸化代谢产物。这是由于耐药细胞中存在缺陷的间型霉素B转运系统。然而,野生型和突变型细胞将[3H]间型霉素A同样有效地掺入含[3H]间型霉素A的核苷酸和RNA中。这些数据表明,间型霉素B在利什曼原虫中的细胞毒性不是通过其作为腺苷类似物掺入RNA来介导的。基于一种必需的细胞内代谢产物的消耗,提出了一种关于吡唑并(4,3-d)嘧啶C-核苷作用机制的合理替代假说。