School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, PR China; International Healthcare Innovation Institute (Jiangmen), Jiangmen 529040, PR China; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, PR China.
School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, PR China; International Healthcare Innovation Institute (Jiangmen), Jiangmen 529040, PR China; Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Biotechnology and Health Sciences, Wuyi University, Jiangmen 529020, PR China.
Bioorg Chem. 2023 Dec;141:106911. doi: 10.1016/j.bioorg.2023.106911. Epub 2023 Oct 9.
Drug-resistant bacterium infections are a severe threat to public health and novel antimicrobial agents combating drug-resistant bacteria are an unmet medical need. Although cannabidiol (CBD) has been reported to show antibacterial effects, whether its antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) can be improved remains unclear. Herein, a series of novel CBD derivatives were designed and synthesized using various chemical approaches including amidation, Friedel-Crafts alkylation, and Negishi cross-coupling reaction for the modifications at the C-7, C-2', C-4', and C-6' positions of CBD skeleton. Derivative 21f showed augmented antibacterial activity against MRSA with a minimum inhibitory concentration of 4 μM without cytotoxic effect in microglia BV2 cells. Further mechanistic studies suggested that 21f inhibited the formation of biofilms, induced excess reactive oxygen species, and reduced bacterial metabolism, which collectively led to the acceleration of bacterial death. Findings from this study expand the understanding of CBD derivatives as promising antibacterial agents, which provides useful information for the development of cannabinoid-based antibacterial agents.
耐药菌感染对公众健康构成严重威胁,而新型抗菌药物对抗耐药菌是未满足的医疗需求。尽管已有报道称大麻二酚(CBD)具有抗菌作用,但尚不清楚其对耐甲氧西林金黄色葡萄球菌(MRSA)的抗菌活性是否可以提高。在此,我们采用酰胺化、傅克烷基化和 Negishi 交叉偶联反应等多种化学方法,对 CBD 骨架的 C-7、C-2'、C-4'和 C-6'位进行修饰,设计并合成了一系列新型 CBD 衍生物。衍生物 21f 对 MRSA 的最小抑菌浓度为 4 μM,同时对小胶质细胞 BV2 细胞没有细胞毒性作用,显示出增强的抗菌活性。进一步的机制研究表明,21f 抑制生物膜的形成,诱导过量的活性氧,并降低细菌代谢,这些共同导致细菌死亡的加速。这项研究的结果扩展了对 CBD 衍生物作为有前途的抗菌剂的认识,为基于大麻素的抗菌剂的开发提供了有用的信息。