Flucofuron as a Promising Therapeutic Agent against Brain-Eating Amoeba

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-05-17 DOI:10.1021/acsinfecdis.4c00062
Javier Chao-Pellicer, Iñigo Arberas-Jiménez, Ines Sifaoui, José E. Piñero* and Jacob Lorenzo-Morales*, 
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Abstract

Primary amoebic meningoencephalitis (PAM) is a rare and fulminant neurodegenerative disease caused by the free-living amoeba Naegleria fowleri. Currently, there is a lack of standardized protocols for therapeutic action. In response to the critical need for effective therapeutic agents, we explored the Global Health Priority Box, a collection of 240 compounds provided by the Medicines for Malaria Venture (MMV). From this pool, flucofuron emerged as a promising candidate, exhibiting high efficacy against trophozoites of both N. fowleri strains (ATCC 30808 IC50 : 2.58 ± 0.64 μM and ATCC 30215 IC50: 2.47 ± 0.38 μM), being even active against the resistant cyst stage (IC50: 0.88 ± 0.07 μM). Moreover, flucofuron induced diverse metabolic events that suggest the triggering of apoptotic cell death. This study highlights the potential of repurposing medications for treating challenging diseases, such as PAM.

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氟虫脲是一种很有前途的食脑阿米巴治疗剂。
原发性阿米巴脑膜脑炎(PAM)是由自由生活的福氏奈格勒阿米巴引起的一种罕见的暴发性神经退行性疾病。目前,还缺乏标准化的治疗方案。为了满足对有效治疗药物的迫切需求,我们研究了全球健康优先药盒(Global Health Priority Box),这是疟疾新药研发公司(MMV)提供的 240 种化合物的集合。在这个化合物库中,氟虫脲是一种很有前途的候选化合物,它对两种 N. fowleri 菌株的滋养体都有很高的疗效(ATCC 30808 IC50:2.58 ± 0.64 μM,ATCC 30215 IC50:2.47 ± 0.38 μM),甚至对抗性囊阶段也有活性(IC50:0.88 ± 0.07 μM)。此外,氟虫脲还能诱导多种新陈代谢事件,这表明它能引发细胞凋亡。这项研究凸显了将药物重新用于治疗具有挑战性的疾病(如 PAM)的潜力。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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