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通过丙磺舒纳米晶体与头孢噻肟钠联合抑制免疫血栓形成促进脓毒症恢复。

Promote Sepsis Recovery through the Inhibition of Immunothrombosis via a Combination of Probenecid Nanocrystals and Cefotaxime Sodium.

作者信息

Meng Zhengjie, Huang Haixiao, Guo Jiaqi, Wang Dong, Tao Xinyue, Dai Qihao, Bai Yunhao, Ma Chenyu, Huang Luming, Fu Yangkai, Lu Chenyu, Wang Hengjian, Wang Qiyue, Li Xueming, Ren Hao

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China.

School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing 211816, China.

出版信息

ACS Appl Mater Interfaces. 2025 Apr 9;17(14):21013-21032. doi: 10.1021/acsami.5c05609. Epub 2025 Mar 28.

Abstract

Sepsis is a life-threatening organ dysfunction syndrome caused by a dysregulated host immune response to pathogenic infection. Due to its high mortality rate, it has been a major global public health problem. Recent studies have shown that the formation of immunothrombosis plays as a "double-edged sword" in the pathogenesis of sepsis, and how to properly regulate immunothrombosis to avoid organ damage and end the high-inflammation state as early as possible are the key steps for sepsis therapy. Considering the complexity of sepsis therapy, the development of an effective combined therapeutic strategy is the goal of this study. First, the insoluble Panexin1 (Panx1) channel inhibitor probenecid (Prob) was prepared as nanocrystals and administered via intramuscular injection. At the same time, septic mice were intravenously injected with cefotaxime sodium through the tail vein for combination therapy. After treatment, the number of infection foci and the level of serum inflammatory factors in septic mice were significantly reduced, and also neutrophil NETosis was significantly inhibited; thus, the survival rate of septic mice was dramatically increased. Pathological analysis revealed that the combination treatment was safe and effective and could significantly reduce the formation of immunothrombosis in septic mice.

摘要

脓毒症是一种由宿主对病原体感染的免疫反应失调引起的危及生命的器官功能障碍综合征。由于其高死亡率,它一直是一个重大的全球公共卫生问题。最近的研究表明,免疫血栓形成在脓毒症发病机制中起着“双刃剑”的作用,如何适当调节免疫血栓形成以避免器官损伤并尽早结束高炎症状态是脓毒症治疗的关键步骤。考虑到脓毒症治疗的复杂性,开发一种有效的联合治疗策略是本研究的目标。首先,将不溶性泛素蛋白1(Panx1)通道抑制剂丙磺舒(Prob)制备成纳米晶体,并通过肌肉注射给药。同时,通过尾静脉对脓毒症小鼠静脉注射头孢噻肟钠进行联合治疗。治疗后,脓毒症小鼠的感染灶数量和血清炎症因子水平显著降低,中性粒细胞胞外诱捕网形成也受到显著抑制;因此,脓毒症小鼠的存活率显著提高。病理分析表明,联合治疗安全有效,可显著减少脓毒症小鼠免疫血栓的形成。

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