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首页> 外文期刊>Acta microbiologica et immunologica Hungarica: A quarterly of the Hungarian Academy of Sciences >Interaction of methylxanthines and gentamicin against Staphylococcus aureus and Pseudomonas aeruginosa: Role of phosphodiesterase inhibition
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Interaction of methylxanthines and gentamicin against Staphylococcus aureus and Pseudomonas aeruginosa: Role of phosphodiesterase inhibition

机译:甲基黄嘌呤和庆大霉素对金黄色葡萄球菌和铜绿假单胞菌的相互作用:磷酸二酯酶抑制作用

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摘要

Previous studies showed that methylxanthines increased the antimicrobial activity of gentamicin against Staphylococcus aureus and Pseudomonas aeruginosa. In this study, the effect of non-selective phosphodiesterase (PDE) inhibitors (methylxanthines: aminophylline and caffeine) and partially selective PDE inhibitors, dipyridamole and sildenafil, was evaluated on the antimicrobial activity of gentamicin using checkerboard method. Aminophylline at concentrations of 0.5 and 1 mg/ml reduced the minimal inhibitory concentration (MIC) of gentamicin (2 μg/ml) 2 and 4 times against S. aureus, and at concentrations of 0.5 and 2 mg/ml reduced the MIC of gentamicin (4 μg/ml) 2 and 4 times, respectively, against P. aeruginosa. Caffeine at concentrations of 1 and 2 mg/ml reduced the MIC of gentamicin (2 μg/ml) 4 and 32 times against S. aureus, and at concentrations of 0.12 and 2 mg/ml reduced the MIC of gentamicin (4 μg/ml) 2 and 4 times, respectively, against P. aeruginosa. However, dipyridamole and sildenafil (32 μg/ml) did not show any effect on MIC of gentamicin against S. aureus and P. aeruginosa. These results suggest that methylxanthines could increase gentamicin effects against S. aureus and P. aeruginosa but this effect is not mediated by inhibition of PDE 5, 6, 8, 10 and 11.
机译:先前的研究表明,甲基黄嘌呤增加了庆大霉素对金黄色葡萄球菌和铜绿假单胞菌的抗菌活性。在这项研究中,使用棋盘法评估了非选择性磷酸二酯酶(PDE)抑制剂(甲基黄嘌呤:氨茶碱和咖啡因)和部分选择性PDE抑制剂双嘧达莫和西地那非对庆大霉素的抗菌活性的影响。浓度为0.5和1 mg / ml的氨茶碱降低了庆大霉素(2μg/ ml)对金黄色葡萄球菌的最小抑菌浓度(MIC)2和4倍,浓度为0.5和2 mg / ml时降低了庆大霉素的MIC (4μg/ ml)分别针对铜绿假单胞菌2次和4次。咖啡因浓度为1和2 mg / ml时,相对于金黄色葡萄球菌,庆大霉素(2μg/ ml)的MIC降低4到32倍;浓度为0.12和2 mg / ml时,庆大霉素的MIC(4μg/ ml)降低)分别对铜绿假单胞菌2次和4次。然而,双嘧达莫和西地那非(32μg/ ml)对庆大霉素对金黄色葡萄球菌和铜绿假单胞菌的MIC没有显示任何作用。这些结果表明甲基黄嘌呤可能增加庆大霉素对金黄色葡萄球菌和铜绿假单胞菌的作用,但这种作用不是由抑制PDE 5、6、8、10和11介导的。

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