黄酮类化合物对致病性自由活阿米巴、福氏奈格丽虫和棘阿米巴的抗阿米巴活性。

0 PARASITOLOGY Parasites, hosts and diseases Pub Date : 2023-11-01 Epub Date: 2023-11-28 DOI:10.3347/PHD.23078
Hương Giang Lê, Tuấn Cường Võ, Jung-Mi Kang, Thu Hằng Nguyễn, Buyng-Su Hwang, Young-Taek Oh, Byoung-Kuk Na
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引用次数: 0

摘要

自由生活的变形虫(FLA)很少引起人类感染,但可以引起中枢神经系统(CNS)的致命感染。对于中枢神经系统FLA感染的治疗尚无共识,因此迫切需要发现或开发安全有效的药物。黄酮类化合物是来自植物及其衍生产品的天然化合物,已知对几种致病性原生动物寄生虫具有抗原生动物活性。黄酮类化合物的抗FLA活性也已被提出,但其对FLA的抗阿米巴活性还有待于实证研究。研究了18种黄酮类化合物对福氏耐格丽虫和棘阿米巴虫(castellanii和多食A. polyhaga)的抗阿米巴活性。这些黄酮类化合物对福氏单胞菌和棘阿米巴具有不同的抗阿米巴活性。去甲氧基姜黄素、山奈酚、白藜芦醇和水飞蓟宾(A+B)对福氏奈瑟菌和棘阿米巴均有体外抗阿米巴活性。芹菜素、木香内酯、(-)-表儿茶素、(-)-表没食子儿茶素、迷迭香酸和(-)-反式石竹烯对棘阿米巴具有选择性抗阿米巴活性。木犀草素对福氏奈瑟菌更有效。然而,黄连素、小檗碱、(±)-儿茶素、chelerythrine、染料木素、(+)-pinostrobin和槲皮素对变形虫没有抗变形虫活性。它们都没有表现出选择性抗阿米巴活性,对C6胶质细胞具有显著的细胞毒性。本研究结果为黄酮类化合物抗FLA活性的研究提供了基础,可用于开发抗FLA感染的替代或补充治疗药物。
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Antiamoebic activities of flavonoids against pathogenic free-living amoebae, Naegleria fowleri and Acanthamoeba species.

Free-living amoebae (FLA) rarely cause human infections but can invoke fatal infections in the central nervous system (CNS). No consensus treatment has been established for FLA infections of the CNS, emphasizing the urgent need to discover or develop safe and effective drugs. Flavonoids, natural compounds from plants and plant-derived products, are known to have antiprotozoan activities against several pathogenic protozoa parasites. The anti-FLA activity of flavonoids has also been proposed, while their antiamoebic activity for FLA needs to be emperically determined. We herein evaluated the antiamoebic activities of 18 flavonoids against Naegleria fowleri and Acanthamoeba species which included A. castellanii and A. polyphaga. These flavonoids showed different profiles of antiamoebic activity against N. fowleri and Acanthamoeba species. Demethoxycurcumin, kaempferol, resveratrol, and silybin (A+B) showed in vitro antiamoebic activity against both N. fowleri and Acanthamoeba species. Apigenin, costunolide, (‒)-epicatechin, (‒)-epigallocatechin, rosmarinic acid, and (‒)-trans-caryophyllene showed selective antiamoebic activity for Acanthamoeba species. Luteolin was more effective for N. fowleri. However, afzelin, berberine, (±)-catechin, chelerythrine, genistein, (+)-pinostrobin, and quercetin did not exhibit antiamoebic activity against the amoeba species. They neither showed selective antiamoebic activity with significant cytotoxicity to C6 glial cells. Our results provide a basis for the anti-FLA activity of flavonoids, which can be applied to develope alternative or supplemental therapeutic agents for FLA infections of the CNS.

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