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半乳糖醇 CSA-13 在尿路感染小鼠模型中表现出很高的抗菌效率。

Ceragenin CSA-13 displays high antibacterial efficiency in a mouse model of urinary tract infection.

机构信息

Department of Medical Microbiology and Nanobiomedical Engineering, Medical University of Białystok, Mickiewicza 2C, 15-222, Białystok, Poland.

Independent Laboratory of Nanomedicine, Medical University of Białystok, Mickiewicza 2B, 15-222, Białystok, Poland.

出版信息

Sci Rep. 2022 Nov 10;12(1):19164. doi: 10.1038/s41598-022-23281-y.

Abstract

Ceragenins (CSAs) are synthetic, lipid-based molecules that display activities of natural antimicrobial peptides. Previous studies demonstrated their high in vitro activity against pathogens causing urinary tract infections (UTIs), but their efficiency in vivo was not explored to date. In this study, we aimed to investigate the bactericidal efficiency of ceragenins against E. coli (Xen14 and clinical UPEC strains) isolates both in vitro and in vivo, as well to explore CSA-13 biodistribution and ability to modulate nanomechanical alterations of infected tissues using animal model of UTI. CSA-44, CSA-131 and particularly CSA-13 displayed potent bactericidal effect against tested E. coli strains, and this effect was mediated by induction of oxidative stress. Biodistribution studies indicated that CSA-13 accumulates in kidneys and liver and is eliminated with urine and bile acid. We also observed that ceragenin CSA-13 reverses infection-induced alterations in mechanical properties of mouse bladders tissue, which confirms the preventive role of CSA-13 against bacteria-induced tissue damage and potentially promote the restoration of microenvironment with biophysical features unfavorable for bacterial growth and spreading. These data justify the further work on employment of CSA-13 in the treatment of urinary tract infections.

摘要

鲨烯醇(CSAs)是一种合成的脂质分子,具有天然抗菌肽的活性。先前的研究表明,它们对引起尿路感染(UTI)的病原体具有很高的体外活性,但迄今为止尚未探索其在体内的效率。在这项研究中,我们旨在研究鲨烯醇对大肠杆菌(Xen14 和临床 UPEC 株)分离株的体外和体内杀菌效率,以及使用尿路感染动物模型探索 CSA-13 的分布和调节感染组织纳米力学变化的能力。CSA-44、CSA-131 尤其是 CSA-13 对测试的大肠杆菌菌株表现出很强的杀菌作用,这种作用是通过诱导氧化应激介导的。分布研究表明,CSA-13 积聚在肾脏和肝脏中,并随尿液和胆汁酸排出体外。我们还观察到,鲨烯醇 CSA-13 逆转了感染诱导的小鼠膀胱组织力学性质的改变,这证实了 CSA-13 对细菌诱导的组织损伤的预防作用,并可能促进具有不利于细菌生长和扩散的生物物理特性的微环境的恢复。这些数据证明了 CSA-13 在治疗尿路感染方面的进一步研究是合理的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4493/9649698/e00da612b1d3/41598_2022_23281_Fig1_HTML.jpg

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