Suppr超能文献

寻找用于治疗恰加斯病的苯硝唑与克氏锥虫磷酸丙糖异构酶抑制剂的组合。

Looking for combination of benznidazole and Trypanosoma cruzi-triosephosphate isomerase inhibitors for Chagas disease treatment.

作者信息

Aguilera Elena, Varela Javier, Serna Elva, Torres Susana, Yaluff Gloria, Bilbao Ninfa Vera de, Cerecetto Hugo, Alvarez Guzmán, González Mercedes

机构信息

Universidad de la República, Facultad de Ciencias, Grupo de Química Medicinal, Montevideo, Uruguay.

Universidad Nacional de Asunción, Instituto de Investigaciones en Ciencias de la Salud, Departamento de Medicina Tropical, Asunción, Paraguay.

出版信息

Mem Inst Oswaldo Cruz. 2018 Mar;113(3):153-160. doi: 10.1590/0074-02760170267.

Abstract

BACKGROUND

The current chemotherapy for Chagas disease is based on monopharmacology with low efficacy and drug tolerance. Polypharmacology is one of the strategies to overcome these limitations.

OBJECTIVES

Study the anti-Trypanosoma cruzi activity of associations of benznidazole (Bnz) with three new synthetic T. cruzi-triosephosphate isomerase inhibitors, 2, 3, and 4, in order to potentiate their actions.

METHODS

The in vitro effect of the drug combinations were determined constructing the corresponding isobolograms. In vivo activities were assessed using an acute murine model of Chagas disease evaluating parasitaemias, mortalities and IgG anti-T. cruzi antibodies.

FINDINGS

The effect of Bnz combined with each of these compounds, on the growth of epimastigotes, indicated an additive action or a synergic action, when combining it with 2 or 3, respectively, and an antagonic action when combining it with 4. In vivo studies, for the two chosen combinations, 2 or 3 plus one fifth equivalent of Bnz, showed that Bnz can also potentiate the in vivo therapeutic effects. For both combinations a decrease in the number of trypomastigote and lower levels of anti-T. cruzi IgG-antibodies were detected, as well clear protection against death.

MAIN CONCLUSIONS

These results suggest the studied combinations could be used in the treatment of Chagas disease.

摘要

背景

目前用于治疗恰加斯病的化疗基于单一药理学,疗效低且存在药物耐受性。多药理学是克服这些局限性的策略之一。

目的

研究苯并硝唑(Bnz)与三种新型合成的克氏锥虫磷酸丙糖异构酶抑制剂2、3和4联合使用时的抗克氏锥虫活性,以增强它们的作用。

方法

通过构建相应的等效线图来确定药物组合的体外效果。使用恰加斯病急性小鼠模型评估寄生虫血症、死亡率和抗克氏锥虫IgG抗体,以评估体内活性。

研究结果

Bnz与这些化合物中的每一种联合使用对前鞭毛体生长的影响表明,与2或3联合使用时分别具有相加作用或协同作用,而与4联合使用时具有拮抗作用。在体内研究中,对于所选的两种组合,即2或3加五分之一当量的Bnz,表明Bnz也可以增强体内治疗效果。对于这两种组合,均检测到锥鞭毛体数量减少和抗克氏锥虫IgG抗体水平降低,以及对死亡的明显保护作用。

主要结论

这些结果表明,所研究的组合可用于治疗恰加斯病。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验