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4-硝基查耳酮对 L. amazonensis 前鞭毛体和细胞内无鞭毛体具有杀利什曼原虫作用,而 4-硝基查耳酮包封于巴西棕榈蜡油纳米粒子中则降低了巨噬细胞的细胞毒性。

4-nitrochalcone exerts leishmanicidal effect on L. amazonensis promastigotes and intracellular amastigotes, and the 4-nitrochalcone encapsulation in beeswax copaiba oil nanoparticles reduces macrophages cytotoxicity.

机构信息

Department of Pathological Sciences, Center of Biological Sciences, State University of Londrina, PR, Brazil.

Department of Pathological Sciences, Center of Biological Sciences, State University of Londrina, PR, Brazil.

出版信息

Eur J Pharmacol. 2020 Oct 5;884:173392. doi: 10.1016/j.ejphar.2020.173392. Epub 2020 Jul 28.

Abstract

The Leishmaniasis treatment currently available involves some difficulties, such as high toxicity, variable efficacy, high cost, therefore, it is crucial to search for new therapeutic alternatives. Over the past few years, research on new drugs has focused on the use of natural compounds such as chalcones and nanotechnology. In this context, this research aimed at assessing the in vitro leishmanicidal activity of free 4-nitrochalcone (4NC) on promastigotes and encapsulated 4NC on L. amazonensis-infected macrophages, as well as their action mechanisms. Free 4NC was able to reduce the viability of promastigotes, induce reactive oxygen species production, decrease mitochondrial membrane potential, increase plasma membrane permeability, and expose phosphatidylserine, in addition to altering the morphology and lowering parasite cellular volume. Treatment containing encapsulated 4NC in beeswax-copaiba oil nanoparticles (4NC-beeswax-CO Nps) did not alter the viability of macrophages. Furthermore, 4NC-beeswax-CO Nps reduced the percentage of infected macrophages and the number of amastigotes per macrophages, increasing the production of reactive oxygen species, NO, TNF-α, and IL-10. Therefore, free 4NC proved to exert anti-promastigote effect, while 4NC-beeswax-CO Nps showed a leishmanicidal effect on L. amazonensis-infected macrophages by activating the macrophage microbicidal machinery.

摘要

目前可用的利什曼病治疗方法存在一些困难,如毒性高、疗效不稳定、成本高,因此,寻找新的治疗方法至关重要。在过去的几年中,新药研究的重点是使用天然化合物,如查耳酮和纳米技术。在这种情况下,本研究旨在评估游离 4-硝基查耳酮(4NC)对前鞭毛体和包裹 4NC 对感染巨噬细胞的利什曼原虫的体外杀利什曼原虫活性,以及它们的作用机制。游离 4NC 能够降低前鞭毛体的活力,诱导活性氧的产生,降低线粒体膜电位,增加质膜通透性,暴露磷脂酰丝氨酸,此外还改变寄生虫的形态并降低细胞体积。在蜂蜡-库帕油纳米粒子(4NC-蜂蜡-CO Nps)中包裹的 4NC 处理不会改变巨噬细胞的活力。此外,4NC-蜂蜡-CO Nps 降低了感染巨噬细胞的百分比和每个巨噬细胞中的无鞭毛体数量,增加了活性氧、NO、TNF-α 和 IL-10 的产生。因此,游离 4NC 被证明对前鞭毛体具有抗活性,而 4NC-蜂蜡-CO Nps 通过激活巨噬细胞杀菌机制对感染利什曼原虫的巨噬细胞表现出杀利什曼原虫作用。

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