利奈唑啉
金黄色葡萄球菌
糖尿病
TLR2型
体内
胰岛素抵抗
药理学
微生物学
医学
胰岛素
炎症
化学
生物
内科学
细菌
内分泌学
万古霉素
遗传学
TLR4型
生物技术
作者
Lihui Ni,Yuan Li,Haifeng Zhang,Yunxiao Ma,Yuli Song,Xudong Tang,Junwen Fan,Jinyang Shi,Xinhua Cui,Hongyue Xu,Hong Zhou,Keshu Shen,Weiying Guo,Lu Yu
标识
DOI:10.1016/j.ijbiomac.2023.124750
摘要
Diabetes mellitus (DM) complicated with Staphylococcus aureus (S. aureus) infection lacks effective treatment strategies. In this study, we found that insulin combined with linezolid has potential to deal with the thorny problem. In vitro, our drug sensitivity assay, bacterial growth curve and hemolytic tests showed that a combination of insulin and linezolid exerted good antibacterial and anti-α-hemolysin activity, CCK8 experiment, glucose content and glycogen content determination showed that the combination of insulin and linezolid increased murine macrophage survival rate and reduced the extracellular glucose level of high glucose-treated MH-S cells and intracellular glycogen level, and Western blot showed that the combination inhibited TLR2/MAPKs/NLRP3-related inflammatory pathways in MH-S cells. The results of in vivo experiments showed that the combination therapy stabilized glucose level, remained body weight, ameliorated lung injury including improving pulmonary edema and decreasing lung wet/dry weight ratio, reduced the CFUs and inflammation in the lung tissue in a mouse model of diabetes with S. aureus pneumonia, and inhibited the expression of TLR2, MAPKs and NLRP3 inflammatory pathway. Overall, the combination of insulin and linezolid as autolytic inhibitor exhibited the effects of significant antibacterial and improving glucose level in vitro and in vivo, and also has an anti-inflammation activity via the TLR2/MAPKs/NLRP3 pathway, this paves the way for new treatments for diabetes mellitus complicated with S. aureus infection.
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