Masadeh Majed M, Alzoubi Karem H, Al-Azzam Sayer I, Khabour Omar F, Al-Buhairan Ahlam M
Department of Pharmaceutical Technology, Jordan University of Science and Technology, Irbid 22110, Jordan.
Department of Clinical Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Pathogens. 2016 Mar 9;5(1):28. doi: 10.3390/pathogens5010028.
Ciprofloxacin works through interfering with replication and transcription of bacterial DNA, which leads to increased oxidative stress, and death of bacterial cells. Drugs with strong antioxidant such as tempol, melatonin and pentoxifylline might interfere with the antibacterial activity of ciprofloxacin. In the current study, the effect of these drugs on the cytotoxicity of ciprofloxacin was investigated against several reference bacteria. Standard bacterial strains included Escherichia coli ATCC 35218, Staphylococcus aureus ATCC29213, Pseudomonas aeruginosa ATCC 9027, Staphylococcus epidermidis ATCC 12228, Acinetobacter baumannii ATCC 17978, Proteus mirabilis ATCC 12459, Klebsiella pneumoniae ATCC 13883, methicillin-resistant Staphylococcus aureus (MRSA) (ATCC 43300), and Streptococcus pneumoniae (ATCC 25923). The antibacterial activity of ciprofloxacin with or without treatment of bacterial cells by tempol, melatonin or pentoxifylline was assessed using the disc diffusion method and by measuring the minimum inhibitory concentration (MIC) and zones of inhibition of bacterial growth. All of the tested bacterial strains were sensitive to ciprofloxacin. When treated with tempol, melatonin or pentoxifylline, all bacterial strains showed significantly smaller zones of inhibition and larger MIC values compared ciprofloxacin alone. In correlation, reactive oxygen species (ROS) generation induced by ciprofloxacin antibacterial action was diminished by treatment of bacterial cells with tempol, melatonin or pentoxifylline. In conclusion, results indicate the possible antagonistic properties for agents with antioxidant properties such as tempol, melatonin and pentoxifylline when they are used concurrently with flouroquinolones. This could be related to the ability of these agents to inhibit oxidative stress in bacterial cells.
环丙沙星通过干扰细菌DNA的复制和转录发挥作用,这会导致氧化应激增加以及细菌细胞死亡。具有强抗氧化作用的药物,如Tempol、褪黑素和己酮可可碱,可能会干扰环丙沙星的抗菌活性。在本研究中,针对几种参考细菌研究了这些药物对环丙沙星细胞毒性的影响。标准细菌菌株包括大肠杆菌ATCC 35218、金黄色葡萄球菌ATCC29213、铜绿假单胞菌ATCC 9027、表皮葡萄球菌ATCC 12228、鲍曼不动杆菌ATCC 17978、奇异变形杆菌ATCC 12459、肺炎克雷伯菌ATCC 13883、耐甲氧西林金黄色葡萄球菌(MRSA)(ATCC 43300)和肺炎链球菌(ATCC 25923)。使用纸片扩散法并通过测量最低抑菌浓度(MIC)和细菌生长抑制圈,评估了环丙沙星在有无Tempol、褪黑素或己酮可可碱处理细菌细胞情况下的抗菌活性。所有测试的细菌菌株对环丙沙星均敏感。当用Tempol、褪黑素或己酮可可碱处理时,与单独使用环丙沙星相比,所有细菌菌株的抑制圈均明显变小,MIC值变大。与此相关的是,用Tempol、褪黑素或己酮可可碱处理细菌细胞可减少环丙沙星抗菌作用诱导产生的活性氧(ROS)。总之,结果表明,具有抗氧化特性的药物,如Tempol、褪黑素和己酮可可碱,与氟喹诺酮类药物同时使用时可能具有拮抗特性。这可能与这些药物抑制细菌细胞氧化应激的能力有关。