Ferulic acid potentiates the antibacterial activity of quinolone-based antibiotics against Acinetobacter baumannii

被引:46
|
作者
Ibitoye, O. B. [1 ]
Ajiboye, T. O. [2 ]
机构
[1] Al Hikmah Univ, Dept Biol Sci, Ilorin, Nigeria
[2] Nile Univ Nigeria, Coll Hlth Sci, Dept Med Biochem, Antioxidants Redox Biol & Toxicol Res Lab, Abuja, Nigeria
关键词
Acinetobacter baumannii; Superoxide dismutase; Catalase; Ferulic acid; Glutathione; Electron transport; OXIDATIVE STRESS; ESCHERICHIA-COLI; PSEUDOMONAS-AERUGINOSA; 2-(2-NITROVINYL) FURAN; BACTERICIDAL ACTIVITY; PHENOLIC-ACIDS; CIPROFLOXACIN; GLUTATHIONE; RESISTANCE; EFFICACY;
D O I
10.1016/j.micpath.2018.11.033
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ferulic acid is a cinnamic derivative of phenolic acid and its pharmacophore (catechol) is responsible for antioxidant, prooxidant and antibacterial activities. In this study, we evaluated the influence of ferulic acid on the antibacterial activity of quinolone-based antibiotics against Acinetobacter baumannii. The minimum inhibitory concentration of ferulic acid against Acinetobacter baumannii AB5075 were considerably lowered for Delta sodB and Delta katG mutants. Checkerboard assay shows synergistic interactions between ferulic acid and quinolones. In a murine sepsis model, ferulic acid potentiated the antibacterial activities of quinolones. Ferulic acid amplified quinolones-induced redox imbalance by increasing superoxide ion generation, NAD + /NADH ratio and ADP/ ATP ratio. Conversely, the level of reduced glutathione was significantly lowered. We conclude that ferulic acid potentiates the antibacterial activity of quinolone-based antibiotics against A. baumannii by increasing ROS generation, energy metabolism and electron transport chain activity with a concomitant decrease in glutathione.
引用
收藏
页码:393 / 398
页数:6
相关论文
共 50 条
  • [1] (+)-Catechin potentiates the oxidative response of Acinetobacter baumannii to quinolone-based antibiotics
    Ibitoye, O. B.
    Ajiboye, T. O.
    MICROBIAL PATHOGENESIS, 2019, 127 : 239 - 245
  • [2] Synthesis and antibacterial activity of quinolone-based compounds containing a coumarin moiety
    Emami, Saeed
    Foroumadi, Alireza
    Faramarzi, Mohammad A.
    Samad, Nasrin
    ARCHIV DER PHARMAZIE, 2008, 341 (01) : 42 - 48
  • [3] Quercetin-Pivaloxymethyl Conjugate Potentiates Antibiotics against Pseudomonas aeruginosa and Acinetobacter baumannii
    Kim, Mi Kyoung
    Jung, Minji
    Park, Ki-Ho
    Chong, Youhoon
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2018, 39 (07) : 879 - 881
  • [4] Potent In Vitro Antibacterial Activity of DS-8587, a Novel Broad-Spectrum Quinolone, against Acinetobacter baumannii
    Higuchi, Saito
    Onodera, Yoshikuni
    Chiba, Megumi
    Hoshino, Kazuki
    Gotoh, Naomasa
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2013, 57 (04) : 1978 - 1981
  • [5] Synergistic Effect of Oleanolic Acid on Aminoglycoside Antibiotics against Acinetobacter baumannii
    Shin, Bora
    Park, Woojun
    PLOS ONE, 2015, 10 (09):
  • [6] Synergistic activity of coriander oil and conventional antibiotics against Acinetobacter baumannii
    Duarte, A.
    Ferreira, S.
    Silva, F.
    Domingues, F. C.
    PHYTOMEDICINE, 2012, 19 (3-4) : 236 - 238
  • [7] Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
    Wang, Leilei
    Chen, Yuancheng
    Han, Renru
    Huang, Zhiwei
    Zhang, Xuefei
    Hu, Fupin
    Yang, Fan
    INFECTION AND DRUG RESISTANCE, 2021, 14 : 3971 - 3977
  • [8] Evaluation of the Antibacterial Activity of New Dermaseptin Derivatives against Acinetobacter baumannii
    Haddad, Houda
    Mejri, Radhia
    Zairi, Amira
    PHARMACEUTICALS, 2024, 17 (02)
  • [9] In vitro antibacterial activity of photoactivated flavonoid glycosides against Acinetobacter baumannii
    Pourhajibagher, Maryam
    Javanmard, Zahra
    Bahador, Abbas
    AMB EXPRESS, 2024, 14 (01):
  • [10] Emerging quinoline- and quinolone-based antibiotics in the light of epidemics
    Kaur, Paranjeet
    Anuradha
    Chandra, Avik
    Tanwar, Tamanna
    Sahu, Sanjeev Kumar
    Mittal, Amit
    CHEMICAL BIOLOGY & DRUG DESIGN, 2022, 100 (06) : 765 - 785