Mahmoudvand Hossein, Shakibaie Mojtaba, Tavakoli Razieh, Jahanbakhsh Sareh, Sharifi Iraj
Research Center for Tropical and Infectious Diseases, Kerman University of Medical Sciences, Kerman, Iran ; Leishmaniasis Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
Iran J Parasitol. 2014 Oct-Dec;9(4):452-60.
Sensitive and glucantime (MA) resistance Leishmania tropica are referred to those isolates, which are responsive, or non-responsive to one or two full courses of treatment by MA systematically and/or intra-lesionally, respectively. In this study, we evaluated the antileishmanial activity of biogenic selenium nanoparticles (Se NPs) alone and in combination with MA against sensitive and glucantime-resistant L. tropica on in vitro model.
The Se NPs were synthesized by employing the Bacillus sp. MSh-1. The antileishmanial effects of Se NPs alone and in combination with MA on promastigote and amastigote stages of sensitive and glucantime-resistant L. tropica strains have been investigated using a colorimetric MTT assay and in a macrophage model. In addition hemolytic activity in type O+ human red blood cells and infectivity rate of the promastigotes before and after treatment with the Se NPs was evaluated.
In the promastigote stage, various concentrations of Se NPs significantly inhibited (P<0.05) the growth of promastigotes of both strains in a dose-dependent manner. Similarly, Se NPs especially in combination with MA significantly reduced the mean number of amastigotes of both strains in each macrophage. Se NPs showed no hemolytic effect on human RBCs at low concentrations. Moreover, infection rate of macrophages by promastigotes significantly (P<0.05) was reduced when promastigotes pre-treated with Se NPs.
The findings of this study suggest a first step in the search of Se NPs as a new antileishmanial agent. Further experiments are needed to investigate antileishmanial effects of biogenic Se NPs on L. tropica using a clinical setting.
对葡糖胺锑(MA)敏感和耐药的热带利什曼原虫是指分别对系统和/或病灶内一或两个完整疗程的MA有反应或无反应的分离株。在本研究中,我们在体外模型中评估了生物源硒纳米颗粒(Se NPs)单独以及与MA联合对敏感和葡糖胺锑耐药的热带利什曼原虫的抗利什曼活性。
利用芽孢杆菌属MSh-1合成Se NPs。使用比色MTT法和巨噬细胞模型研究了Se NPs单独以及与MA联合对敏感和葡糖胺锑耐药的热带利什曼原虫前鞭毛体和无鞭毛体阶段的抗利什曼作用。此外,还评估了Se NPs处理前后O+型人红细胞的溶血活性以及前鞭毛体的感染率。
在前鞭毛体阶段,不同浓度的Se NPs均以剂量依赖方式显著抑制(P<0.05)两株原虫前鞭毛体的生长。同样,Se NPs尤其是与MA联合显著降低了每个巨噬细胞内两株原虫无鞭毛体的平均数量。低浓度时Se NPs对人红细胞无溶血作用。此外,用Se NPs预处理前鞭毛体后,巨噬细胞被前鞭毛体感染的比率显著降低(P<0.05)。
本研究结果表明在寻找Se NPs作为一种新型抗利什曼药物方面迈出了第一步。需要进一步实验以在临床环境中研究生物源Se NPs对热带利什曼原虫的抗利什曼作用。