Department of Pharmacognosy with Medicinal Plant Unit, Medical University of Lublin, 20-093 Lublin, Poland.
Department of Biochemistry and Biotechnology, Medical University of Lublin, 20-093 Lublin, Poland.
Molecules. 2018 Jan 15;23(1):176. doi: 10.3390/molecules23010176.
: On account of emergence of multi- and extensively drug-resistant (Mtb) strains, combinations of drugs with natural compounds were tested to search for antibiotic activity enhancers. In this work we studied terpenes (α-pinene, bisabolol, β-elemene, ()-limonene, ()-limonene, myrcene, sabinene), which are the main constituents of essential oil obtained from L., a plant with described antitubercular activity, to investigate their interactions with antibiotics against reference Mtb strains and multidrug-resistant clinical isolates. : The serial dilution method was used to evaluate the minimal inhibitory concentration (MIC) of tested compounds, while the fractional inhibitory concentration index (FICI) was calculated for characterization of interactions. Moreover, IC values of tested compounds were determined using monkey kidney epithelial cell line (GMK). : The combinations of all studied terpenes with ethambutol or rifampicin resulted in a synergistic interaction. Bisabolol and ()-limonene decreased the MIC for rifampicin at least two-fold for all tested strains, however no synergistic action was observed against virulent strains. The tested terpenes showed slight (bisabolol) or no cytotoxic effect against normal eukaryotic cells in vitro. : The obtained enhanced activity (FICI < 0.5) of ethambutol and rifampicin against H37Ra strain under the influence of the studied terpenes may be correlated to the capability of essential oil constituents to modify bacterial resistance mechanisms in general. The observed differences in avirulent and virulent bacteria susceptibility to terpenes tested separately and in combinations with antibiotics can be correlated with the differences in the cell wall structure between H37Ra mutant and all virulent strains.
: 由于出现了多药耐药和广泛耐药的(Mtb)菌株,人们测试了药物与天然化合物的组合,以寻找抗生素活性增强剂。在这项工作中,我们研究了萜类化合物(α-蒎烯、双醇、β-榄香烯、()-柠檬烯、()-柠檬烯、月桂烯、柠檬烯),它们是从 L. 中获得的精油的主要成分,该植物具有描述的抗结核活性,以研究它们与抗生素对参考 Mtb 菌株和多药耐药临床分离株的相互作用。: 使用连续稀释法评估测试化合物的最小抑菌浓度(MIC),同时计算分数抑菌浓度指数(FICI)以表征相互作用。此外,还使用猴肾上皮细胞系(GMK)测定了测试化合物的 IC 值。: 所有研究的萜类化合物与乙胺丁醇或利福平的组合均表现出协同作用。双醇和()-柠檬烯使所有测试菌株的利福平 MIC 降低至少两倍,但对毒力菌株没有观察到协同作用。测试的萜类化合物在体外对正常真核细胞显示出轻微(双醇)或无细胞毒性作用。: 在研究的萜类化合物的影响下,H37Ra 株中乙胺丁醇和利福平的活性增强(FICI<0.5)可能与精油成分普遍改变细菌耐药机制的能力有关。单独测试的萜类化合物以及与抗生素联合使用时对无毒和有毒细菌的敏感性的差异可能与 H37Ra 突变体与所有有毒菌株之间细胞壁结构的差异有关。