Khayat Maan T, Abbas Hisham A, Ibrahim Tarek S, Elbaramawi Samar S, Khayyat Ahdab N, Alharbi Majed, Hegazy Wael A H, Yehia Fatma Al-Zahraa A
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Zagazig 44519, Egypt.
Biomedicines. 2023 May 14;11(5):1442. doi: 10.3390/biomedicines11051442.
The repurposing of drugs is one of the most competent strategies for discovering new antimicrobial agents. Vildagliptin is a dipeptidyl peptidase-4 inhibitor (DPI-4) that is used effectively in combination with metformin to control blood glucose levels in diabetic patients. This study was designed to evaluate the anti-virulence activities of this combination against one of the most clinically important pathogens, . The current findings show a significant ability of the vildagliptin-metformin combination to diminish biofilm formation, bacterial motility, and the production of virulent extracellular enzymes and pyocyanin pigment. Furthermore, this drug combination significantly increased the susceptibility of to oxidative stress, indicating immunity enhancement in the eradication of bacterial cells. In compliance with the in vitro findings, the histopathological photomicrographs of mice showed a considerable protective effect of the metformin-vildagliptin combination against , revealing relief of inflammation due to -induced pathogenesis. mainly employs quorum sensing (QS) systems to control the production of its huge arsenal of virulence factors. The anti-virulence activities of the metformin-vildagliptin combination can be interrupted by the anti-QS activities of both metformin and vildagliptin, as both exhibited a considerable affinity to QS receptors. Additionally, the metformin-vildagliptin combination significantly downregulated the expression of the main three QS-encoding genes in . These findings show the significant anti-virulence activities of metformin-vildagliptin at very low concentrations (10, 1.25 mg/mL, respectively) compared to the concentrations (850, 50 mg/mL, respectively) used to control diabetes.
药物的重新利用是发现新型抗菌剂最有效的策略之一。维格列汀是一种二肽基肽酶-4抑制剂(DPP-4),可与二甲双胍联合有效用于控制糖尿病患者的血糖水平。本研究旨在评估该联合用药对一种临床上最重要的病原体的抗毒力活性。目前的研究结果表明,维格列汀-二甲双胍联合用药具有显著降低生物膜形成、细菌运动性以及有毒细胞外酶和绿脓菌素产生的能力。此外,这种药物组合显著增加了该病原体对氧化应激的敏感性,表明在根除细菌细胞方面增强了免疫力。与体外研究结果一致,小鼠的组织病理学显微照片显示二甲双胍-维格列汀组合对该病原体具有相当大的保护作用,揭示了因该病原体诱导的发病机制而导致的炎症减轻。该病原体主要利用群体感应(QS)系统来控制其大量毒力因子的产生。二甲双胍和维格列汀的抗QS活性可中断二甲双胍-维格列汀组合的抗毒力活性,因为二者均对QS受体表现出相当大的亲和力。此外,二甲双胍-维格列汀组合显著下调了该病原体中主要三个QS编码基因的表达。这些研究结果表明,与用于控制糖尿病的浓度(分别为850、50mg/mL)相比,二甲双胍-维格列汀在非常低的浓度(分别为10、1.25mg/mL)下具有显著的抗毒力活性。