金黄色葡萄球菌感染诱发中性粒细胞氧化失衡:纳米共轭万古霉素的可能保护作用。

ISRN Pharmacology Pub Date : 2012-01-01 Epub Date: 2012-03-15 DOI:10.5402/2012/435214
Subhankari Prasad Chakraborty, Panchanan Pramanik, Somenath Roy
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引用次数: 0

摘要

金黄色葡萄球菌感染会导致中性粒细胞氧化应激。免疫细胞利用活性氧(ROS)来执行其正常功能,而过量的 ROS 会攻击细胞成分,导致细胞损伤。本研究旨在检测纳米万古霉素对万古霉素敏感金黄色葡萄球菌(VSSA)和万古霉素耐药金黄色葡萄球菌(VRSA)感染诱导的中性粒细胞氧化应激的保护作用。通过腹腔注射 5 × 10(6) CFU/mL 的细菌溶液,在瑞士小鼠体内形成 VSSA 和 VRSA 感染。纳米共轭万古霉素以其有效剂量治疗 VSSA 和 VRSA 感染小鼠 10 天。万古霉素以相似的剂量分别治疗 VSSA 和 VRSA 感染小鼠 10 天。结果显示,与对照组相比,体内 VSSA 和 VRSA 感染会显著增加脂质过氧化水平、蛋白质氧化水平、氧化谷胱甘肽水平和亚硝酸盐的生成,并降低还原谷胱甘肽水平、抗氧化酶状态和谷胱甘肽依赖酶;而纳米结合万古霉素处理组的还原谷胱甘肽水平则显著增加或降低,接近正常水平。这些发现表明,纳米结合万古霉素对 VSSA 和 VRSA 感染诱导的中性粒细胞氧化失衡具有潜在的用途和有益的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Staphylococcus aureus Infection Induced Oxidative Imbalance in Neutrophils: Possible Protective Role of Nanoconjugated Vancomycin.

Staphylococcus aureus Infection Induced Oxidative Imbalance in Neutrophils: Possible Protective Role of Nanoconjugated Vancomycin.

Staphylococcus aureus Infection Induced Oxidative Imbalance in Neutrophils: Possible Protective Role of Nanoconjugated Vancomycin.

Staphylococcus aureus Infection Induced Oxidative Imbalance in Neutrophils: Possible Protective Role of Nanoconjugated Vancomycin.

Staphylococcus aureus infection causes oxidative stress in neutrophils. The immune cells use reactive oxygen species (ROS) for carrying out their normal functions while an excess amount of ROS can attack cellular components that lead to cell damage. The present study was aimed to test the protective role of nanoconjugated vancomycin against vancomycin-sensitive Staphylococcus aureus (VSSA) and vancomycin-resistant Staphylococcus aureus (VRSA) infection induced oxidative stress in neutrophils. VSSA- and VRSA-infection were developed in Swiss mice by intraperitoneal injection of 5 × 10(6) CFU/mL bacterial solutions. Nanoconjugated vancomycin was treated to VSSA- and VRSA-infected mice at its effective dose for 10 days. Vancomycin was treated to VSSA and VRSA infected mice at similar dose, respectively, for 10 days. The result reveals that in vivo VSSA and VRSA infection significantly increases the level of lipid peroxidation, protein oxidation, oxidized glutathione level, and nitrite generation and decreases the level of reduced glutathione, antioxidant enzyme status, and glutathione-dependent enzymes as compared to control group; which were increased or decreased significantly near to normal in nanoconjugated vancomycin-treated group. These finding suggests the potential use and beneficial protective role of nanoconjugated vancomycin against VSSA and VRSA infection induced oxidative imbalance in neutrophils.

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