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Axenically Grown Amastigotes of Leishmania infantum Used as an In Vitro Model To Investigate the Pentavalent Antimony Mode of Action

机译:婴幼儿利什曼原虫的轴生生长的拟南芥用作体外模型研究五价锑的作用方式

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摘要

The mechanism(s) of activity of pentavalent antimony [Sb(V)] is poorly understood. In a recent study, we have shown that potassium antimonyl tartrate, a trivalent antimonial [Sb(III)], was substantially more potent than Sb(V) against both promastigotes and axenically grown amastigotes of three Leishmania species, supporting the idea of an in vivo metabolic conversion of Sb(V) into Sb(III). We report that amastigotes of Leishmania infantum cultured under axenic conditions were poorly susceptible to meglumine [Glucantime; an Sb(V)], unlike those growing inside THP-1 cells (50% inhibitory concentrations [IC50s], about 1.8 mg/ml and 22 μg/ml, respectively). In order to define more precisely the mode of action of Sb(V) agents in vivo, we first induced in vitro Sb(III) resistance by direct drug pressure on axenically grown amastigotes of L. infantum. Then we determined the susceptibilities of both extracellular and intracellular chemoresistant amastigotes to the Sb(V)-containing drugs meglumine and sodium stibogluconate plus m-chlorocresol (Pentostam). The chemoresistant amastigotes LdiR2, LdiR10, and LdiR20 were 14, 26, and 32 times more resistant to Sb(III), respectively, than the wild-type one (LdiWT). In accordance with the hypothesis described above, we found that intracellular chemoresistant amastigotes were resistant to meglumine [Sb(V)] in proportion to the initial level of Sb(III)-induced resistance. By contrast, Sb(III)-resistant cells were very susceptible to sodium stibogluconate. This lack of cross-resistance is probably due to the presence in this reagent of m-chlorocresol, which we found to be more toxic than Sb(III) to L. infantum amastigotes (IC50s, of 0.54 and 1.32 μg/ml, respectively). Collectively, these results were consistent with the hypothesis of an intramacrophagic metabolic conversion of Sb(V) into trivalent compounds, which in turn became readily toxic to the Leishmania amastigote stage.
机译:对五价锑[Sb(V)]的活性机理了解甚少。在最近的一项研究中,我们表明,酒石酸锑基锑酸钾(一种三价锑[Sb(III)])对三种利什曼原虫的前鞭毛体和无性繁殖的拟变体都比Sb(V)更有效,支持了Sb(V)体内代谢转化为Sb(III)。我们报告说,在轴索性条件下培养的婴儿利什曼原虫的变形虫对葡甲胺的敏感性很低[Glucantime; Sb(V)],不同于在THP-1细胞内部生长的Sb(V)](50%抑制浓度[IC50s]分别约为1.8 mg / ml和22μg/ ml)。为了更精确地定义Sb(V)剂在体内的作用方式,我们首先通过直接药压对婴儿乳杆菌L. axenically生长的变形虫诱导了体外Sb(III)耐药性。然后,我们确定了细胞外和细胞内化学抗性吻合剂对含Sb(V)的药物葡甲胺和司考葡糖酸钠加间氯甲酚(Pentostam)的敏感性。化学抗性吻合子LdiR2,LdiR10和LdiR20对Sb(III)的抵抗力分别是野生型(LdiWT)的14倍,26倍和32倍。根据上述假设,我们发现细胞内化学抗性吻合子对葡甲胺[Sb(V)]的抗性与Sb(III)诱导的抗性的初始水平成比例。相比之下,抗Sb(III)的细胞对司他葡糖酸钠非常敏感。这种交叉抗性的缺乏可能是由于该试剂中存在间氯甲酚,我们发现它比Sb(III)对婴儿乳杆菌具有更强的毒性(IC50分别为0.54和1.32μg/ ml)。 。总体而言,这些结果与Sb(V)的宏内吞噬代谢转化为三价化合物的假说相符,而三价化合物反过来容易对利什曼原虫假肢体阶段产生毒性。

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