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Synergistic effects of silver ions and metformin against enterococcus faecalis under high-glucose conditions in vitro
BACKGROUND: This study aimed to evaluate the synergistic antibacterial activities of silver ions (Ag(+)) and metformin hydrochloride (Met) against Enterococcus faecalis (E. faecalis) under normal or high-glucose conditions. RESULTS: The minimum inhibitory concentration, minimum bactericidal concentr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482635/ https://www.ncbi.nlm.nih.gov/pubmed/34587895 http://dx.doi.org/10.1186/s12866-021-02291-2 |
Sumario: | BACKGROUND: This study aimed to evaluate the synergistic antibacterial activities of silver ions (Ag(+)) and metformin hydrochloride (Met) against Enterococcus faecalis (E. faecalis) under normal or high-glucose conditions. RESULTS: The minimum inhibitory concentration, minimum bactericidal concentration, growth curves, and colony-forming units were used to evaluate the antibacterial effects of Ag(+) and Met on planktonic E. faecalis in Brain Heart Infusion broth with or without additional glucose. The influences of Ag(+) and Met on four weeks E. faecalis biofilm on human dentin slices was also tested. Cytotoxicity was tested on MC3T3-E1 osteoblastic cells using CCK-8 assays. The results indicated that E. faecalis showed higher resistance to drug treatment under high-glucose conditions. Ag(+) (40 μg/mL) plus Met (3.2% or 6.4%) showed enhanced antibacterial activities against both planktonic E. faecalis and biofilm on dentin slices, with low cytotoxicity. CONCLUSIONS: Met enhanced the bactericidal effects of Ag(+) against both planktonic and biofilm E. faecalis under normal or high-glucose conditions with low cytotoxicity. Further molecular studies are needed to be conducted to understand the mechanisms underlying the synergistic activity between Met and Ag(+). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02291-2. |
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