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齐留通,一种5-脂氧合酶抑制剂,具有抗寄生虫作用,并可预防恰加斯病慢性期的炎症。

Zileuton, a 5-Lypoxigenase Inhibitor, is Antiparasitic and Prevents Inflammation in the Chronic Stage of Heart Chagas Disease.

作者信息

Ricci Mayra Fernanda, Lourenço Estela Mariana Guimarães, Pereira Rafaela das Dores, Araújo Ronan Ricardo Sabino, Oliveira Fernando Bento Rodrigues, Barbosa da Silva Elany, de Oliveira Gabriel Stephani, Teixeira Mauro Martins, Rocha Nazareth de Novaes, Chambergo Felipe Santiago, Roman-Campos Danilo, Cruz Jader Santos, Ferreira Rafaela Salgado, Machado Fabiana Simão

机构信息

Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Minas Gerais, Brazil.

Department of Microbiology, Institute of Biomedical Sciences, Universidade de São Paulo, São Paulo 05508-000, Brazil.

出版信息

ACS Infect Dis. 2024 Dec 13;10(12):4258-4270. doi: 10.1021/acsinfecdis.4c00623. Epub 2024 Nov 28.

Abstract

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 infection by acting directly on the parasite and reducing heart damage and is a promising option for the treatment of Chagas disease.

摘要

慢性恰加斯心肌病与免疫反应失衡和心脏功能受损有关,且现有药物无法阻止其发展。齐留通(Zi)是一种5-脂氧合酶抑制剂,可影响炎症/促消退介质。在此,感染早期进行Zi治疗可降低寄生虫血症,这主要与Zi对寄生虫的直接作用有关,环氧水解酶是杀锥虫作用背后的潜在分子靶点。在感染的中间急性期,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,并改善了心脏功能。在慢性期开始的Zi治疗增加了心脏中SOCS2的表达水平,减轻了炎症,并改善了心脏功能。我们的数据表明,Zi通过直接作用于寄生虫并减少心脏损伤来预防感染,是治疗恰加斯病的一个有前景的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c304/11650774/9ecbb99f0362/id4c00623_0001.jpg

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