Zileuton是一种5-溶氧酶抑制剂,具有抗寄生虫和预防心脏恰加斯病慢性期炎症的作用。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-12-13 Epub Date: 2024-11-28 DOI:10.1021/acsinfecdis.4c00623
Mayra Fernanda Ricci, Estela Mariana Guimarães Lourenço, Rafaela das Dores Pereira, Ronan Ricardo Sabino Araújo, Fernando Bento Rodrigues Oliveira, Elany Barbosa da Silva, Gabriel Stephani de Oliveira, Mauro Martins Teixeira, Nazareth de Novaes Rocha, Felipe Santiago Chambergo, Danilo Roman-Campos, Jader Santos Cruz, Rafaela Salgado Ferreira, Fabiana Simão Machado
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引用次数: 0

摘要

慢性恰加斯心肌病与免疫反应不平衡和心功能受损有关,现有药物无法阻止其发展。Zileuton (Zi)是一种5-溶氧酶抑制剂,影响炎症/促溶解介质。因此,在感染早期处理Zi减少了寄生虫血症,这主要与Zi对寄生虫的直接作用有关,环氧化物水解酶是锥虫作用背后的潜在分子靶点。在感染的中急性期,Zi减少了先天性和适应性炎症细胞的数量,增加了心脏中与较低炎症相关的SOCS2表达水平,改善了心功能。在慢性期开始的Zi治疗增加了心脏中SOCS2的表达水平,减少了炎症,改善了心功能。我们的数据表明,Zi通过直接作用于寄生虫和减少心脏损伤来预防克氏锥虫感染,是治疗恰加斯病的一个有希望的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zileuton, a 5-Lypoxigenase Inhibitor, is Antiparasitic and Prevents Inflammation in the Chronic Stage of Heart Chagas Disease.

Chronic Chagas cardiomyopathy is associated with an unbalanced immune response and impaired heart function, and available drugs do not prevent its development. Zileuton (Zi), a 5-lypoxigenase inhibitor, affects inflammatory/pro-resolution mediators. Herein, Zi treatment in the early phase of infection reduced parasitemia associated mainly with the direct effect of Zi on the parasite, and the enzyme epoxide hydrolase was the potential molecular target behind the trypanocidal effect. In the intermediate acute phase of infection, Zi reduced the number of innate and adaptive inflammatory cells, increased the level of SOCS2 expression in the heart associated with lower inflammation, and improved cardiac function. Zi treatment initiated in the chronic stage increased the level of SOCS2 expression in the heart, reduced inflammation, and improved cardiac function. Our data suggest that Zi protects against Trypanosoma cruzi infection by acting directly on the parasite and reducing heart damage and is a promising option for the treatment of Chagas disease.

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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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