Synthesis and Biological Evaluation of Cyanoacrylamides and 5-Iminopyrrol-2-Ones Against Naegleria fowleri.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-09-13 Epub Date: 2024-08-08 DOI:10.1021/acsinfecdis.4c00439
Javier Chao-Pellicer, Samuel Delgado-Hernández, Iñigo Arberas-Jiménez, Ines Sifaoui, David Tejedor, Fernando García-Tellado, José E Piñero, Jacob Lorenzo-Morales
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Abstract

Primary amoebic meningoencephalitis is caused by the free-living amoeba Naegleria fowleri. The lack of standardized treatment has significantly contributed to the high fatality rates observed in reported cases. Therefore, this study aims to explore the anti-Naegleria activity of eight synthesized cyanoacrylamides and 5-iminopyrrol-2-ones. Notably, QOET-109, QOET-111, QOET-112, and QOET-114 exhibited a higher selectivity index against Naegleria compared to those of the rest of the compounds. Subsequently, these chemicals were assessed against the resistant stage of N. fowleri, demonstrating activity similar to that observed in the vegetative stage. Moreover, characteristic events of programmed cell death were evidenced, including chromatin condensation, increased plasma membrane permeability, mitochondrial damage, and heightened oxidative stress, among others. Finally, this research demonstrated the in vitro activity of the cyanoacrylamide and 5-iminopyrrol-2-one molecules, as well as the induction of metabolic event characteristics of regulated cell death in Naegleria fowleri.

Abstract Image

氰基丙烯酰胺和 5-氨基吡咯-2-酮的合成及对 Naegleria fowleri 的生物学评价。
原发性阿米巴脑膜脑炎是由自由生活的福氏纳格勒阿米巴引起的。由于缺乏标准化的治疗方法,导致报告病例中的死亡率居高不下。因此,本研究旨在探索八种合成的氰基丙烯酰胺和 5-亚氨基吡咯-2-酮的抗奈格勒氏菌活性。值得注意的是,与其他化合物相比,QOET-109、QOET-111、QOET-112 和 QOET-114 对奈格勒氏菌具有更高的选择性。随后,对这些化学物质进行了针对 N. fowleri 耐药阶段的评估,结果显示其活性与在无性阶段观察到的活性相似。此外,还发现了细胞程序性死亡的特征事件,包括染色质凝结、质膜通透性增加、线粒体损伤和氧化应激增强等。最后,这项研究证明了氰基丙烯酰胺和 5-亚氨基吡咯-2-酮分子的体外活性,以及诱导 Naegleria fowleri 调节性细胞死亡的代谢事件特征。
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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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