Wang Nuoyan, Luo Jing, Deng Fei, Huang Yasi, Zhou Hong
Key Laboratory of Basic Pharmacology, Ministry of Education and Joint Laboratory of International Cooperation, Ministry of Education of Characteristic Ethnic Medicine, School of Pharmacy, Zunyi Medical University, Zunyi, China.
Front Pharmacol. 2022 Feb 23;13:839808. doi: 10.3389/fphar.2022.839808. eCollection 2022.
After the first aminoglycoside antibiotic streptomycin being applied in clinical practice in the mid-1940s, aminoglycoside antibiotics (AGAs) are widely used to treat clinical bacterial infections and bacterial resistance to AGAs is increasing. The bacterial resistance to AGAs is owed to aminoglycoside modifying enzyme modification, active efflux pump gene overexpression and 16S rRNA ribosomal subunit methylation, leading to modification of AGAs' structures and decreased concentration of drugs within bacteria. As AGAs's side effects and bacterial resistance, the development of AGAs is time-consuming and difficult. Because bacterial resistance may occur in a short time after application in clinical practice, it was found that the antibacterial effect of the combination was not only better than that of AGAs alone but also reduce the dosage of antibiotics, thereby reducing the occurrence of side effects. This article reviews the clinical use of AGAs, the antibacterial mechanisms, the molecular mechanisms of bacterial resistance, and especially focuses a recent development of the combination of AGAs with other drugs to exert a synergistic antibacterial effect to provide a new strategy to overcome bacterial resistance to AGAs.
20世纪40年代中期第一种氨基糖苷类抗生素链霉素应用于临床实践后,氨基糖苷类抗生素(AGAs)被广泛用于治疗临床细菌感染,且细菌对AGAs的耐药性正在增加。细菌对AGAs的耐药性归因于氨基糖苷类修饰酶修饰、主动外排泵基因过表达和16S rRNA核糖体亚基甲基化,导致AGAs结构改变以及细菌内药物浓度降低。由于AGAs的副作用和细菌耐药性,AGAs的研发耗时且困难。由于临床实践中应用后短时间内可能出现细菌耐药性,发现联合用药的抗菌效果不仅优于单独使用AGAs,还能减少抗生素剂量,从而减少副作用的发生。本文综述了AGAs的临床应用、抗菌机制、细菌耐药的分子机制,尤其重点介绍了AGAs与其他药物联合发挥协同抗菌作用的最新进展,以提供克服细菌对AGAs耐药性的新策略。