Department of Molecular Genetics, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, The Netherlands.
Department of Clinical Microbiology, Instituto de Investigación Biosanitaria ibs. GRANADA, University Hospital Clínico San Cecilio, Granada, Spain.
J Enzyme Inhib Med Chem. 2023 Dec;38(1):267-281. doi: 10.1080/14756366.2022.2146685.
Antimicrobial resistance is a global concern, far from being resolved. The need of new drugs against new targets is imminent. In this work, we present a family of aminoalkyl resveratrol derivatives with antibacterial activity inspired by the properties of cationic amphipathic antimicrobial peptides. Surprisingly, the newly designed molecules display modest activity against aerobically growing bacteria but show surprisingly good antimicrobial activity against anaerobic bacteria (Gram-negative and Gram-positive) suggesting specificity towards this bacterial group. Preliminary studies into the action mechanism suggest that activity takes place at the membrane level, while no cross-resistance with traditional antibiotics is observed. Actually, some good synergistic relations with existing antibiotics were found against Gram-negative pathogens. However, some cytotoxicity was observed, despite their low haemolytic activity. Our results show the importance of the balance between positively charged moieties and hydrophobicity to improve antimicrobial activity, setting the stage for the design of new drugs based on these molecules.
抗菌耐药性是一个全球性的问题,远未得到解决。我们迫切需要针对新靶点的新药。在这项工作中,我们展示了一系列具有抗菌活性的氨基酸烷基白藜芦醇衍生物,其灵感来自于阳离子两亲性抗菌肽的特性。令人惊讶的是,新设计的分子对需氧生长的细菌表现出适度的活性,但对厌氧细菌(革兰氏阴性和革兰氏阳性)表现出惊人的良好抗菌活性,表明它们对这种细菌具有特异性。对作用机制的初步研究表明,活性发生在膜水平,而与传统抗生素没有交叉耐药性。实际上,在针对革兰氏阴性病原体的研究中发现了一些与现有抗生素的良好协同关系。然而,尽管它们的溶血活性较低,还是观察到了一些细胞毒性。我们的结果表明,在正电荷部分和疏水性之间取得平衡对于提高抗菌活性非常重要,为基于这些分子设计新药奠定了基础。