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增强抗生素对金黄色葡萄球菌的活性:卡彭花椒的成分及衍生物

Enhancing activity of antibiotics against Staphylococcus aureus: Zanthoxylum capense constituents and derivatives.

作者信息

Cabral Vanessa, Luo Xuan, Junqueira Elisabete, Costa Sofia S, Mulhovo Silva, Duarte Aida, Couto Isabel, Viveiros Miguel, Ferreira Maria-José U

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisboa, Portugal.

Grupo de Micobactérias, Unidade de Microbiologia Médica, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Rua da Junqueira 100, 1349-008 Lisboa, Portugal.

出版信息

Phytomedicine. 2015 Apr 15;22(4):469-76. doi: 10.1016/j.phymed.2015.02.003. Epub 2015 Mar 5.

Abstract

Six compounds (1-6), isolated from the methanol extract of the roots of the African medicinal plant Zanthoxylum capense Thunb. (Rutaceae), and seven ester derivatives (7-13) were evaluated for their antibacterial activities and modulatory effects on the MIC of antibiotics (erythromycin, oxacillin, and tetracycline) and ethidium bromide (EtBr) against a Staphylococcus aureus reference strain (ATCC 6538). Using the same model, compounds 1-13 were also assessed for their potential as efflux pump inhibitors by a fluorometric assay that measures the accumulation of the broad range efflux pump substrate EtBr. Compounds 8 and 11 were further evaluated for their antibacterial, modulatory and EtBr accumulation effects against four additional S. aureus strains, which included two clinical methicillin-resistant S. aureus (MRSA) strains. Compounds (1-13) have not shown antibacterial activity at the concentration ranges tested. When evaluated against S. aureus ATCC 6538, oxychelerythrine (1) a benzophenanthridine alkaloid, showed the highest modulatory activity enhancing the susceptibility of this strain to all the tested antibiotics from two to four-fold. Ailanthoidiol diacetate (8) and ailanthoidiol di-2-ethylbutanoate (11) were also good modulators when combined with EtBr, increasing the bacteria susceptibility by four and two-fold, respectively. In the EtBr accumulation assay, using ATCC 6538 strain, the phenylpropanoid (+)-ailanthoidiol (6) and most of its ester derivatives (8-11) exhibited higher activity than the positive control verapamil. The highest effects were found for compounds 8 and 11 that also increased the accumulation of EtBr, using S. aureus ATCC 25923 as model. Furthermore, both compounds (8, 11) were able to enhance the ciprofloxacin activity against the MRSA clinical strains tested, causing a reduction of the antibiotic MIC values from two to four-fold. The EtBr accumulation assay revealed that this modulation activity was not due to an inhibition of efflux pumps mechanism. These results suggested that Z. capense constituents may be valuable as leads for restoring antibiotic activity against MRSA strains.

摘要

从非洲药用植物刺花椒(芸香科)根部的甲醇提取物中分离出六种化合物(1-6),并对七种酯衍生物(7-13)进行了抗菌活性评估,以及它们对金黄色葡萄球菌参考菌株(ATCC 6538)的抗生素(红霉素、苯唑西林和四环素)和溴化乙锭(EtBr)最低抑菌浓度(MIC)的调节作用评估。使用相同模型,还通过测量广谱外排泵底物EtBr积累的荧光测定法评估了化合物1-13作为外排泵抑制剂的潜力。进一步评估了化合物8和11对另外四种金黄色葡萄球菌菌株的抗菌、调节和EtBr积累作用,其中包括两种临床耐甲氧西林金黄色葡萄球菌(MRSA)菌株。在测试的浓度范围内,化合物(1-13)未显示出抗菌活性。当针对金黄色葡萄球菌ATCC 6538进行评估时,苯并菲啶生物碱氧化白屈菜红碱(1)表现出最高的调节活性,使该菌株对所有测试抗生素的敏感性提高了两到四倍。与EtBr联合使用时,臭椿二醇二乙酸酯(8)和臭椿二醇二-2-乙基丁酸酯(11)也是良好的调节剂,分别使细菌敏感性提高了四倍和两倍。在使用ATCC 6538菌株的EtBr积累试验中,苯丙烷类化合物(+)-臭椿二醇(6)及其大多数酯衍生物(8-11)表现出比阳性对照维拉帕米更高的活性。以金黄色葡萄球菌ATCC 25923为模型,化合物8和11的效果最为显著,它们也增加了EtBr的积累。此外,两种化合物(8, 11)都能够增强环丙沙星对测试的MRSA临床菌株的活性,使抗生素MIC值降低两到四倍。EtBr积累试验表明,这种调节活性不是由于抑制外排泵机制所致。这些结果表明,刺花椒的成分可能作为恢复针对MRSA菌株抗生素活性的先导物具有重要价值。

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