(+) - α -蒎烯对干扰蛋白质合成和细菌遗传物质的抗菌剂活性的调节作用

T. Farias, Felipe Lemos Esteves do Amaral, S. Ferreira
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引用次数: 0

摘要

发现具有抗菌活性的新分子以及了解其作用机制是对抗多重耐药病原体的重要策略。α-蒎烯的正对映体似乎是对抗它们的一种选择,因为它抑制微生物的生长,包括金黄色葡萄球菌菌株,这使得它有可能作为一种抗菌剂,单独使用或与其他药物联合使用。因此,本研究的主要目的是评估(+)- α -蒎烯对作用于蛋白质合酶和干扰细菌遗传物质的合成抗菌素活性的调节作用。采用改良圆盘扩散法研究了(+)- α -蒎烯对部分金黄色葡萄球菌临床用抗生素活性的调节作用。碟片含有以下抗菌剂:环丙沙星5 μg、四环素30 μg、呋喃妥因300 μg和利福平5 μg。将50微升(+)- α -蒎烯(160µL/mL)加入到含有抗菌剂的磁盘中,验证单萜烯的调节作用。在植物成分和四种被测抗菌剂之间的关联中观察到不同的活性。还需要进一步研究新的方法来评价(+)- α -蒎烯与商业抗菌剂之间的关联的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulating effect of (+) – α – pinene on the activity of antimicrobials that interfere on protein synthesis and bacterial genetic material
The discovery of new molecules with antimicrobial activity, and the understanding of the mechanisms of action, are important strategies against multiresistant pathogens. The positive enantiomer of α-pinene appears as an alternative to combat them, since it inhibits the growth of microorganisms, including strains of S. aureus, which gives the possibility of its use as an antimicrobial agent, isolated or in combination with other drugs. Therefore, the main goal of this study is to evaluate the modulating effect of (+)–α–pinene on the activity of synthetic antimicrobials that act on protein synthase and interfere with bacterial genetic material. The modulating effect of (+)–α–pinene on the activity of antibiotics for clinical use on some S. aureus strains was studied using the modified disc-diffusion method. The disks contain the following antimicrobials: Ciprofloxacin 5 μg, Tetracycline 30 μg, Nitrofurantoin 300 μg and Rifampicin 5 μg. 50 microliters of (+) - alpha-pinene (160 µL/mL) were added to the disks containing the antimicrobials to verify the modulating effect of monotrepene. Indifferent activity was observed in the association between the phytoconstituent and the four tested antimicrobials. Further studies using new methods in order to evaluate the antimicrobial activity of the association between the (+)–α–pinene and commercial antimicrobials are still needed.
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