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Effects of combined therapy with thalidomide and glucantime on leishmaniasis induced by Leishmania major in BALB/c mice

机译:沙利度胺和葡聚糖胺联合治疗对BALB / c小鼠大利什曼原虫诱导的利什曼病的影响

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摘要

For treating Leishmania major infection in BALB/c mice, we used thalidomide in conjunction with glucantime. Groups of mice were challenged with 5 × 103 metacyclic promastigotes of L. major subcutaneously. A week after the challenge, drug treatment was started and continued for 12 days. Thalidomide was orally administrated 30 mg/kg/day and glucantime was administrated intraperitoneally (200 mg/kg/day). It was shown that the combined therapy is more effective than single therapies with each one of the drugs since the foot pad swelling in the group of mice received thalidomide and glucantime was significantly decreased (0.9 ± 0.2 mm) compared to mice treated with either glucantime, thalidomide, or carrier alone (1.2 ± 0.25, 1.4 ± 0.3, and 1.7 ± 0.27 mm, respectively). Cytokine study showed that the effect of thalidomide was not dependent on IL-12; however, it up-regulated IFN-γ and down-regulated IL-10 production. Conclusively, thalidomide seems promising as a conjunctive therapy with antimony in murine model of visceral leishmaniasis.
机译:为了治疗BALB / c小鼠中的利什曼原虫重大感染,我们将沙利度胺与葡聚糖疗法联合使用。皮下注射5×10 3 大环乳酸前体鞭毛体攻击小鼠。攻击后一周,药物治疗开始并持续12天。沙利度胺口服30 mg / kg /天,葡聚糖时间腹膜内给药(200 mg / kg /天)。结果表明,与两种药物中的每一种相比,联合疗法比单一疗法更有效,因为与使用两种葡聚糖治疗的小鼠相比,接受沙利度胺治疗的小鼠足垫肿胀和葡聚糖时间明显减少(0.9±0.2 mm),沙利度胺或单独的载体(分别为1.2±0.25、1.4±0.3和1.7±0.27 mm)。细胞因子研究表明,沙利度胺的作用不依赖于IL-12。然而,它上调了IFN-γ,下调了IL-10的产生。结论是沙利度胺有望在内脏利什曼病鼠模型中作为锑的联合疗法。

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