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首页> 外文期刊>Pathogens and disease[electronic] >Combination of kaempferol and azithromycin attenuates Staphylococcus aureus-induced osteomyelitis via anti-biofilm effects and by inhibiting the phosphorylation of ERK1/2 and SAPK
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Combination of kaempferol and azithromycin attenuates Staphylococcus aureus-induced osteomyelitis via anti-biofilm effects and by inhibiting the phosphorylation of ERK1/2 and SAPK

机译:山柰酚和阿奇霉素变弱葡萄球菌aureus-induced通过anti-biofilm效应和骨髓炎抑制ERK1/2的磷酸化和SAPK

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摘要

Osteomyelitis is bacterial infection of bone, commonly caused by Staphylococcus aureus. This work aims to study the potential of azithromycin and kaempferol against chronic osteomyelitis induced by azithromycin-resistant Staphylococcus aureus (ARSA). It was noticed that rats tolerated the treatments with no diarrhoea or weight loss; also, no deaths were observed in rats. The treatment by azithromycin alone failed to inhibit bacterial growth and also had no effect on the infection condition of bone, although the treatment decreased the levels of interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α), but did not improve the oxidative stress levels. Kaempferol monotherapy slightly inhibited bacterial growth and bone infection; the treatment also inhibited the levels of IL-6 and (TNF-α). The treatment also improved the antioxidant status. However, the combined treatment of azithromycin and kaempferol significantly suppressed bacterial growth and bone infection and modulated oxidative stress. In vitro, the combined treatment inhibited the levels of IL-6 and TNF-α, and also suppressed the phosphorylation of ERK1/2 and stress-activated protein kinase (SAPK). The combined treatment also showed anti-biofilm activity in ARSA. The combination attenuates ARSA-induced osteomyelitis in rats compared with their treatments alone by reducing oxidative stress, inhibiting the phosphorylation of ERK1/2 and SAPK and inhibiting biofilm formation.
机译:骨髓炎是骨头的细菌感染,通常由金黄色葡萄球菌引起的。工作的目的是研究阿奇霉素的潜力和山柰酚对慢性骨髓炎引起azithromycin-resistant金黄色葡萄葡萄球菌(ARSA)。没有腹泻的治疗或减肥;同样,没有观察到大鼠死亡。仅靠阿奇霉素治疗未能抑制细菌生长,也没有影响感染的骨,虽然治疗减少白细胞介素- 6的水平(il - 6)和肿瘤坏死因子-α(TNF -α),但是没有改善氧化应激水平。山柰酚单药治疗轻微抑制细菌生长和骨感染;治疗也抑制il - 6的水平(TNF -α)。抗氧化状态。阿奇霉素和山柰酚治疗显著抑制细菌生长骨感染和调节氧化应激。体外,结合治疗抑制了水平的il - 6和TNF -α,也抑制了磷酸化ERK1/2和压力激发了蛋白激酶(SAPK)。还显示在ARSA anti-biofilm活动。结合变弱ARSA-induced骨髓炎仅在老鼠相比,他们的治疗减少氧化应激,抑制的磷酸化ERK1/2 SAPK和抑制生物膜的形成。

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