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烟酰胺对脱氧核糖核酸酶I的激活作用作为一种减轻……四环素抗性生物膜的新策略

Activation of Deoxyribonuclease I by Nicotinamide as a New Strategy to Attenuate Tetracycline-Resistant Biofilms of .

作者信息

Shih Yi-Hsien, Liu Donald, Chen Yen-Chou, Liao Ming-Hsuan, Lee Woan-Ruoh, Shen Shing-Chuan

机构信息

Department of Dermatology, Taipei Medical University Shuang Ho Hospital, New Taipei City 23561 Taiwan.

Department of Dermatology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.

出版信息

Pharmaceutics. 2021 May 31;13(6):819. doi: 10.3390/pharmaceutics13060819.

Abstract

Biofilms of () (formerly ) are responsible for the persistence and antibiotic resistance of acne vulgaris. In addition to the standard treatments for acne vulgaris, a common adjunctive treatment is the topical administration of nicotinamide (NAM). However, the effects of NAM on biofilms of have never been explored. This study comprehensively investigates the effects of NAM against biofilms of using in vitro and in vivo approaches. The results showed that NAM potentiated the efficacy of suboptimal dosing of tetracycline against . Moreover, NAM alone decreased the formation and increased the degradation of biofilms in . The antibiofilm effect of NAM against was further enhanced in combination with deoxyribonuclease (DNase) I, an enzyme with known antibiofilm properties. The computational molecular docking, surface plasmon resonance analysis, and enzymatic kinetic assay demonstrated that NAM binds to DNase I and accelerated its reaction. In conclusion, NAM activates DNase I to attenuate biofilms of . This offers valuable insights into the strategies against biofilms that are worth elaborating on in other biofilm-related chronic cutaneous infections in the future.

摘要

痤疮丙酸杆菌(以前称为痤疮棒状杆菌)的生物膜是寻常痤疮持续存在和产生抗生素耐药性的原因。除了寻常痤疮的标准治疗方法外,一种常见的辅助治疗是局部应用烟酰胺(NAM)。然而,NAM对痤疮丙酸杆菌生物膜的影响从未被研究过。本研究使用体外和体内方法全面研究了NAM对痤疮丙酸杆菌生物膜的影响。结果表明,NAM增强了次优剂量四环素对痤疮丙酸杆菌的疗效。此外,单独使用NAM可减少痤疮丙酸杆菌生物膜的形成并增加其降解。NAM与具有已知抗生物膜特性的脱氧核糖核酸酶(DNase)I联合使用时,其对痤疮丙酸杆菌的抗生物膜作用进一步增强。计算分子对接、表面等离子体共振分析和酶动力学测定表明,NAM与DNase I结合并加速其反应。总之,NAM激活DNase I以减轻痤疮丙酸杆菌的生物膜。这为对抗生物膜的策略提供了有价值的见解,值得在未来其他与生物膜相关的慢性皮肤感染中进一步阐述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4fe/8228415/8f6e4abc7124/pharmaceutics-13-00819-g001.jpg

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