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两种联苯化合物原苏木素A和B与苏木对耐甲氧西林金黄色葡萄球菌菌株的抗菌活性及抗生素协同作用

Antimicrobial activity and synergy of antibiotics with two biphenyl compounds, protosappanins A and B from Sappan Lignum against methicillin-resistant Staphylococcus aureus strains.

作者信息

Zuo Guo-Ying, Han Zong-Qi, Han Jun, Hao Xiao-Yan, Tang Hua-Shu, Wang Gen-Chun

机构信息

Research Center for Natural Medicines, Kunming General Hospital of Chengdu Military Command, Kunming, China.

School of Pharmacy, Guiyang Medical University, Guiyang, China.

出版信息

J Pharm Pharmacol. 2015 Oct;67(10):1439-47. doi: 10.1111/jphp.12433. Epub 2015 Apr 29.

Abstract

OBJECTIVES

This study aims to investigate antimicrobial ingredients from Sappan Lignum and to evaluate their synergy on methicillin-resistant Staphylococcus aureus strains with antibiotics.

METHODS

Bioactivity-guided phytochemical procedures were used to screen the active compounds. Minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) were assayed by broth microdilution. The synergy was evaluated through checkerboard microdilution and loss of viability assays.

KEY FINDINGS

Protosappanins A (PsA) and B (PsB) were identified from Sappan Lignum extracts. They showed active against both S. aureus and MRSA with MIC or MIC50 at 64 (PsA) and 128 (PsB) mg/L alone. When they were used in combination with antibiotics, they showed best synergy with amikacin and gentamicin with MIC50 (mg/L) of amikacin reduced more significantly from 32 to four (with PsA) and eight (with PsB), and the fractional inhibitory concentration index (FICI) ranged between 0.078 and 0.500 (FICI50  = 0.375). Moreover, the resistance of MRSA towards amikacin and gentamicin could be reversed by the Clinical and Laboratory Standards Institute criteria. The combined bactericidal mode could as well be synergy. PsA and PsB showed very low cytotoxicity in comparison with their promising activity against MRSA.

CONCLUSIONS

Protosappanins A and B showed both alone activities and resistance reversal effects of amikacin and gentamicin against MRSA, which warrant further investigations for potential combinatory therapy of MRSA infection.

摘要

目的

本研究旨在研究苏木中的抗菌成分,并评估其与抗生素对耐甲氧西林金黄色葡萄球菌菌株的协同作用。

方法

采用生物活性导向的植物化学方法筛选活性化合物。通过肉汤微量稀释法测定最低抑菌浓度(MIC)和最低杀菌浓度(MBC)。通过棋盘微量稀释法和活力丧失试验评估协同作用。

主要发现

从苏木提取物中鉴定出原苏木素A(PsA)和原苏木素B(PsB)。它们对金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌均有活性,单独使用时MIC或MIC50分别为64(PsA)和128(PsB)mg/L。当它们与抗生素联合使用时,与阿米卡星和庆大霉素表现出最佳协同作用,阿米卡星的MIC50(mg/L)从32显著降低至4(与PsA联合)和8(与PsB联合),部分抑菌浓度指数(FICI)在0.078至0.500之间(FICI50 = 0.375)。此外,根据临床和实验室标准协会标准,耐甲氧西林金黄色葡萄球菌对阿米卡星和庆大霉素的耐药性可被逆转。联合杀菌模式也可能是协同作用。与它们对耐甲氧西林金黄色葡萄球菌的良好活性相比,PsA和PsB的细胞毒性非常低。

结论

原苏木素A和B单独表现出活性,且对耐甲氧西林金黄色葡萄球菌具有逆转阿米卡星和庆大霉素耐药性的作用,这值得进一步研究用于耐甲氧西林金黄色葡萄球菌感染的潜在联合治疗。

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