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首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Anti- Helicobacter pylori activity of ethoxzolamide
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Anti- Helicobacter pylori activity of ethoxzolamide

机译:乙氧唑胺的抗幽门螺杆菌活性

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Ethoxzolamide (EZA), acetazolamide, and methazolamide are clinically used sulphonamide drugs designed to treat non-bacteria-related illnesses (e.g. glaucoma), but they also show antimicrobial activity against the gastric pathogen Helicobacter pylori. EZA showed the highest activity, and was effective against clinical isolates resistant to metronidazole, clarithromycin, and/or amoxicillin, suggesting that EZA kills H. pylori via mechanisms different from that of these antibiotics. The frequency of single-step spontaneous resistance acquisition by H. pylori was less than 5?×?10-9, showing that resistance to EZA does not develop easily. Resistance was associated with mutations in three genes, including the one that encodes undecaprenyl pyrophosphate synthase, a known target of sulphonamides. The data indicate that EZA impacts multiple targets in killing H. pylori. Our findings suggest that developing the approved anti-glaucoma drug EZA into a more effective anti-H. pylori agent may offer a faster and cost-effective route towards new antimicrobials with a novel mechanism of action.
机译:Ethoxzolamide(EZA),acetazolamide和methazolamide是临床上用于治疗非细菌性相关疾病(例如青光眼)的磺胺类药物,但它们也显示出对胃病原体幽门螺杆菌的抗菌活性。 EZA表现出最高的活性,并且对耐甲硝唑,克拉霉素和/或阿莫西林的临床分离株有效,表明EZA通过不同于这些抗生素的机制杀死幽门螺杆菌。幽门螺杆菌获得的单步自发抗性的频率小于5π×Δ10-9,这表明对EZA的抗性不容易发展。抗药性与三个基因的突变有关,包括一个编码十一碳烯基焦磷酸合酶(一种已知的磺酰胺靶标)的基因。数据表明,EZA在杀死幽门螺杆菌方面会影响多个目标。我们的发现表明,将批准的抗青光眼药物EZA开发为更有效的抗H药物。幽门螺杆菌药物可能会提供一种新颖的作用机制,以更快,更具成本效益的方式开发新的抗菌药物。

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