开发具有抗革兰氏阳性菌膜破坏作用的黄原酮醇衍生化合物

Siyu Yang, Fangquan Liu, Yue Leng, Meiyue Zhang, Lei Zhang, Xuekun Wang, Yinhu Wang
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引用次数: 0

摘要

耐多药病原体引起的感染已成为公共卫生的严重威胁。为了开发新的抗菌剂来对抗此类耐药细菌,研究人员通过模仿抗菌肽(AMPs)的结构和功能,设计并合成了一类新型两亲性黄原酮醇衍生化合物。其中,化合物 9h 对测试的革兰氏阳性菌株显示出卓越的抗菌活性(MICs = 0.5-2 μg/mL),与万古霉素相当,且溶血性毒性低,膜选择性好。此外,化合物 9h 还具有快速杀菌作用、低耐药频率、低细胞毒性和良好的血浆稳定性。机理研究进一步发现,化合物 9h 具有良好的膜靶向能力,能够破坏细菌细胞膜的完整性,导致细胞内 ROS 增加、DNA 和蛋白质泄漏,从而加速细菌死亡。这些结果使 9h 成为一种很有希望的抗菌候选物质,可用于抗击细菌感染。
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Development of Xanthoangelol-Derived Compounds with Membrane-Disrupting Effects against Gram-Positive Bacteria
Infections caused by multidrug-resistant pathogens have emerged as a serious threat to public health. To develop new antibacterial agents to combat such drug-resistant bacteria, a class of novel amphiphilic xanthoangelol-derived compounds were designed and synthesized by mimicking the structure and function of antimicrobial peptides (AMPs). Among them, compound 9h displayed excellent antimicrobial activity against the Gram-positive strains tested (MICs = 0.5–2 μg/mL), comparable to vancomycin, and with low hemolytic toxicity and good membrane selectivity. Additionally, compound 9h demonstrated rapid bactericidal effects, low resistance frequency, low cytotoxicity, and good plasma stability. Mechanistic studies further revealed that compound 9h had good membrane-targeting ability and was able to destroy the integrity of bacterial cell membranes, causing an increase in intracellular ROS and the leakage of DNA and proteins, thus accelerating bacterial death. These results make 9h a promising antimicrobial candidate to combat bacterial infection.
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