Biosciences and Biotechnology Postgraduate Program, Carlos Chagas Institute, (ICC/Fiocruz/PR), Curitiba, Paraná, Brazil; State University of Londrina (UEL/PR), Laboratory of Immunoparasitology, Londrina, Paraná, Brazil.
Biosciences and Biotechnology Postgraduate Program, Carlos Chagas Institute, (ICC/Fiocruz/PR), Curitiba, Paraná, Brazil; State University of Londrina (UEL/PR), Laboratory of Immunoparasitology, Londrina, Paraná, Brazil.
Phytomedicine. 2019 Apr;57:262-270. doi: 10.1016/j.phymed.2018.12.035. Epub 2018 Dec 31.
BACKGROUND: Leishmaniasis is a disease caused by protozoan parasites of the Leishmania genus whose current treatment has high cost, highly toxic, and difficult administration, which makes it very important to find alternative natural compounds of high efficiency and low cost. PURPOSE: This study assessed the in vitro effect of caffeic acid (CA) on promastigotes and L. amazonensis-infected macrophages. METHODS: Evaluation of the in vitro leishmanicidal activity of CA against promastigotes and L. amazonensis infected peritoneal macrophages, as well its microbicide mechanisms. RESULTS: CA 12.5-100 µg/ml were able to inhibit promastigotes proliferation at all tested periods. The IC, 12.5 µg/ml, also altered promastigote cell morphology and cell volume accompanied by loss of mitochondrial integrity, increase in reactive oxygen species (ROS) production, phosphatidylserine exposure, and loss of plasma membrane integrity - characterizing the apoptosis-like process. Moreover, CA reduced the percentage of infected macrophages and the number of amastigotes per macrophages increasing TNF-α, ROS, NO and reducing IL-10 levels as well as iron availability. CONCLUSION: CA showed in vitro antipromastigote and antiamostigote by increasing oxidant and inflammatory response important to eliminate the parasite.
背景:利什曼病是一种由利什曼原虫属原生动物寄生虫引起的疾病,目前的治疗方法成本高、毒性大且给药困难,因此寻找高效、低成本的替代天然化合物非常重要。
目的:本研究评估了咖啡酸(CA)对前鞭毛体和感染巨噬细胞的 L. amazonensis 的体外作用。
方法:评估 CA 对前鞭毛体和感染的 L. amazonensis 腹腔巨噬细胞的体外杀利什曼原虫活性及其杀菌机制。
结果:CA 在所有测试时间点的 12.5-100μg/ml 浓度下均能抑制前鞭毛体的增殖。IC₅₀为 12.5μg/ml,还改变了前鞭毛体的形态和细胞体积,同时伴随着线粒体完整性丧失、活性氧(ROS)产生增加、磷脂酰丝氨酸暴露和质膜完整性丧失,表现出类似凋亡的过程。此外,CA 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 TNF-α、ROS、NO 的水平,降低了 IL-10 的水平,并降低了铁的可用性。
结论:CA 通过增加氧化应激和炎症反应显示出体外抗前鞭毛体和抗无鞭毛体作用,这对于消除寄生虫很重要。
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