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抗结核药物:减少外排=增强活性。

Antituberculosis drugs: reducing efflux=increasing activity.

作者信息

Rodrigues Liliana, Parish Tanya, Balganesh Meenakshi, Ainsa José A

机构信息

Grupo de Genética de Micobacterias, Departamento de Microbiología, Medicina Preventiva y Salud Pública, Facultad de Medicina and BIFI, Universidad de Zaragoza, Zaragoza, Spain; CIBER Enfermedades Respiratorias (CIBERES), Madrid, Spain; Fundación Agencia Aragonesa para la Investigación y Desarrollo (ARAID), Zaragoza, Spain.

TB Discovery Research, Infectious Disease Research Institute, Seattle, WA, USA.

出版信息

Drug Discov Today. 2017 Mar;22(3):592-599. doi: 10.1016/j.drudis.2017.01.002. Epub 2017 Jan 13.

Abstract

In mycobacteria, it was assumed that efflux pumps only had a marginal role in drug resistance. In recent years, owing to the need to find novel drugs against multidrug-resistant tuberculosis, it has become clear that efflux should not be ignored. Although efflux inhibitors have been very useful for characterizing in vitro the properties of efflux pumps, their usefulness in vivo is limited because of their toxicity. Alternatively, programs aimed at discovering novel drugs for treating tuberculosis should implement strategies to characterize efflux liability of candidate drugs. Here, we present an experimental approach for studying efflux of compounds selected under the More Medicines for Tuberculosis research project, and a few examples of how, for tuberculosis drug discovery, efflux matters.

摘要

在分枝杆菌中,人们曾认为外排泵在耐药性方面仅起次要作用。近年来,由于需要寻找针对耐多药结核病的新型药物,外排现象显然不应被忽视。尽管外排抑制剂对于在体外表征外排泵的特性非常有用,但由于其毒性,它们在体内的效用有限。另外,旨在发现治疗结核病新药的项目应实施策略来表征候选药物的外排倾向。在此,我们提出一种实验方法,用于研究在“更多结核病药物”研究项目下所选化合物的外排情况,并举例说明外排在结核病药物研发中的重要性。

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