噻唑衍生物作为隐球菌病治疗的有希望的候选者。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2025-03-14 Epub Date: 2025-02-07 DOI:10.1021/acsinfecdis.4c00732
Victor Augusto Teixeira Leocádio, Isabela L Miranda, Martha H C Magalhães, Valtair Severino Dos Santos Júnior, José Eduardo Goncalves, Renata Barbosa Oliveira, Vinicius Gonçalves Maltarollo, Rafael Wesley Bastos, Gustavo Goldman, Susana Johann, Nalu Teixeira de Aguiar Peres, Daniel de Assis Santos
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引用次数: 0

摘要

隐球菌病是一种严重的真菌感染,主要由两种被包膜的酵母菌引起:新型隐球菌和加蒂隐球菌。最严重的并发症是隐球菌性脑膜炎,真菌穿过血脑屏障,导致严重的脑部感染。目前的治疗方法,包括两性霉素B和氟胞嘧啶或氟康唑,通常是有毒的,不是很有效。因此,迫切需要新的抗真菌药物。本研究筛选了30种噻唑类衍生物对隐球菌的抗真菌活性及其对脑细胞的毒性。4个化合物(RN86、RN88、RJ37和RVJ42)表现出特别强的作用。这些化合物降低了真菌膜中的麦角甾醇水平,抑制了其穿过血脑屏障的能力。值得注意的是,RN86和RVJ42通过降低肺和脑中的真菌负荷来提高隐球菌病小鼠模型的存活率。这些发现表明,这些衍生物可能是治疗肺和神经隐球菌病的有希望的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiazole Derivatives as Promising Candidates for Cryptococcosis Therapy.

Cryptococcosis is a severe fungal infection primarily caused by two encapsulated yeasts: Cryptococcus neoformans and C. gattii. The most significant complication is cryptococcal meningitis, where the fungus crosses the blood-brain barrier, leading to a severe brain infection. Current treatments, which include amphotericin B and flucytosine or fluconazole, are often toxic and not very effective. Therefore, there is a pressing need for new antifungal agents. This study screened 30 thiazole derivatives for their antifungal activity against Cryptococcus and their toxicity to brain cells. Four compounds (RN86, RN88, RJ37, and RVJ42) showed particularly strong effects. These compounds reduced ergosterol levels in the fungal membrane and inhibited its ability to cross the blood-brain barrier. Notably, RN86 and RVJ42 improved survival rates in a mouse model of cryptococcosis by lowering the fungal load in the lungs and brain. These findings suggest that these derivatives could be promising treatments for pulmonary and neurocryptococcosis.

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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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