Anti-leishmania Effect of Magnesium Oxide Nanoparticles on Leishmania tropica/infantum and Leishmania-Infected Macrophages

Amir Karimipour-Saryazdi, Mohammad Jafari, Roya Omidi, F. Ghaffarifar, Seyyed Hojjat Sadeghi
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引用次数: 2

Abstract

Background: Leishmania is an intracellular protozoan parasite that enters and reproduces in macrophage cells. Macrophages are important immune cells that phagocyte many pathogens such as bacteria, fungi, and parasites such as Leishmania spp. but are incapable of killing this parasite, living in the phagosomes of infected macrophages, multiplying, and resulting in the divesting of infected macrophages and the appearance of Leishmania lesions. Many of the present drugs for Leishmania treatment have side effects, or parasites have resistance to some of these drugs. Therefore, there is a need for a better drug for Leishmania treatment. Magnesium oxide (MgO) is a metal nanoparticle (NP) with numerous biological applications, including antioxidant and antimicrobial effects on various pathogens such as some bacteria, fungi, and parasites, including Leishmania spp. Objectives: Accordingly, this article has discussed the effects of MgO NPs on Leishmania tropica and Leishmania infantum and Leishmania-infected macrophages. Materials and Methods: The effect of various doses of MgO NPs on L. tropica and L. infantum promastigotes and amastigotes was studied in vitro. Flow cytometry and MTT were also utilized to assess the cytotoxic effects of MgO on L. tropica and L. infantum promastigotes, as well as the likelihood of apoptosis. Amastigote assay was employed to determine the infected macrophage percentage, and the number of parasites present in every macrophage cell. Results: The percentage of macrophages contaminated with amastigotes of L. tropica and L. infantum that were treated with MgO NPs was 15% and 11%, respectively. Flow cytometry revealed that MgO NPs induced approximately 38.56% and 30.5% apoptosis on L. tropica and Leishmania infantum, respectively. The half maximal inhibitory concentration of MgO NPs to L. tropica and L. infantum according to promastigote assay for 72 hours was 7.32 μg/mL and 12.58 μg/mL, respectively. Conclusion: According to the findings, MgO NPs had a great in-vitro fatality effect on L. tropica and L. infantum promastigotes and amastigotes (inside leishmania-infected macrophages).
氧化镁纳米颗粒对热带利什曼原虫/婴儿和感染利什曼原虫巨噬细胞的抗利什曼原虫作用
背景:利什曼原虫是一种进入巨噬细胞并在巨噬细胞中繁殖的细胞内原生动物寄生虫。巨噬细胞是重要的免疫细胞,可以吞噬许多病原体,如细菌、真菌和寄生虫,如利什曼原虫,但不能杀死这种寄生虫,生活在被感染的巨噬细胞的吞噬体中,繁殖,导致被感染的巨噬细胞剥离,出现利什曼原虫病变。目前治疗利什曼原虫的许多药物都有副作用,或者寄生虫对其中一些药物有耐药性。因此,需要一种更好的利什曼原虫治疗药物。氧化镁(MgO)是一种具有多种生物学应用的金属纳米颗粒(NP),包括对各种病原体(如一些细菌、真菌和寄生虫,包括利什曼原虫)的抗氧化和抗菌作用。目的:因此,本文讨论了氧化镁纳米颗粒对热带利什曼原虫、婴儿利什曼原虫和感染利什曼原虫的巨噬细胞的影响。材料与方法:在体外研究了不同剂量MgO NPs对热带乳杆菌和婴儿乳杆菌原鞭毛菌和无尾鞭毛菌的影响。流式细胞术和MTT也被用来评估MgO对热带乳杆菌和婴儿乳杆菌的细胞毒性作用,以及细胞凋亡的可能性。采用无毛线虫实验测定感染的巨噬细胞百分比,以及每个巨噬细胞中存在的寄生虫数量。结果:MgO NPs处理后,被热带乳杆菌和婴儿乳杆菌无尾线虫污染的巨噬细胞比例分别为15%和11%。流式细胞术显示,MgO NPs分别诱导热带L.和婴儿利什曼原虫38.56%和30.5%的细胞凋亡。promastigote法测定MgO NPs对热带乳杆菌和婴儿乳杆菌72 h的半最大抑制浓度分别为7.32 μg/mL和12.58 μg/mL。结论:MgO NPs对热带乳杆菌和婴儿乳杆菌(感染利什曼的巨噬细胞内)的原乳糜虫和无尾乳糜虫具有较强的体外致死作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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