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异土木香内酯单独及联合用药对结核分枝杆菌的体外活性。

In vitro activity of isoimperatorin, alone and in combination, against Mycobacterium tuberculosis.

机构信息

Department of Food Quality and Safety, College of Quartermaster Technology, Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun, China.

出版信息

Lett Appl Microbiol. 2014 Apr;58(4):344-9. doi: 10.1111/lam.12195. Epub 2013 Dec 12.

Abstract

UNLABELLED

Previous studies have shown that isoimperatorin (IO), a furanocoumarin isolated from several medicinal plants, has antimycobacterial activity against Mycobacterium tuberculosis strain H37Rv (ATCC 27294). This study demonstrated that IO has antimycobacterial activity against 2 drug-sensitive and 6 drug-resistant isolates, with minimum inhibitory concentrations (MICs) of 50-100 μg ml(-1) and 100-200 μg ml(-1), respectively. IO exhibited synergistic antimycobacterial effects with rifampin (RMP), isoniazid (INH) and ethambutol (EMB) against 6 drug-resistant strains, with fractional inhibitory concentration index (FICI) values of 0·133-0·472, 0·123-0·475 and 0·124-0·25, respectively. The IO/RMP, IO/INH and IO/EMB combination treatments had synergistic effects or no interaction in the 2 drug-sensitive strains and the standard strain ATCC 27294. The synergism of combined drugs against drug-resistant strains was better than drug-sensitive strains. No antagonism was observed in with the aforementioned combinations against all strains tested. IO exhibited relatively low cytotoxicity to Vero cells. Our results indicate that IO may serve as promising a template for future antimycobacterial drug development.

SIGNIFICANCE AND IMPACT OF THE STUDY

This is the first report on the in vitro synergistic antimycobacterial effects of isoimperatorin (IO) in combination with three first-line drugs: rifampin (RMP), isoniazid (INH) and ethambutol (EMB). The results indicated that the antimycobacterial activity of IO was modest; however, IO was a useful and effective agent against Myco. tuberculosis when it was combined with first-line antimycobacterial drugs and is worthy of further development as a lead compound for the development of novel antimycobacterial therapeutic agents.

摘要

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先前的研究表明,异欧前胡素(IO),一种从几种药用植物中分离出来的呋喃香豆素,对结核分枝杆菌 H37Rv(ATCC 27294)具有抗分枝杆菌活性。本研究表明,IO 对 2 种药敏和 6 种耐药分离株具有抗分枝杆菌活性,最低抑菌浓度(MIC)分别为 50-100μg/ml 和 100-200μg/ml。IO 与利福平(RMP)、异烟肼(INH)和乙胺丁醇(EMB)联合对 6 种耐药株具有协同抗分枝杆菌作用,其部分抑菌浓度指数(FICI)值分别为 0.133-0.472、0.123-0.475 和 0.124-0.25。IO/RMP、IO/INH 和 IO/EMB 联合治疗在 2 种药敏株和标准株 ATCC 27294 中具有协同作用或无相互作用。联合药物对耐药株的协同作用优于药敏株。在所有测试菌株中,未观察到上述组合的拮抗作用。IO 对 Vero 细胞的细胞毒性相对较低。我们的结果表明,IO 可能成为未来抗分枝杆菌药物开发的有前途的模板。

研究的意义和影响

这是首次报道异欧前胡素(IO)与三种一线药物:利福平(RMP)、异烟肼(INH)和乙胺丁醇(EMB)联合的体外协同抗分枝杆菌作用。结果表明,IO 的抗分枝杆菌活性适中;然而,当 IO 与一线抗分枝杆菌药物联合使用时,它是一种对抗结核分枝杆菌有效的药物,作为开发新型抗分枝杆菌治疗药物的先导化合物值得进一步开发。

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