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乳酸作为生物膜抑制剂:通过蛋白质组学/代谢组学及毒性研究对其作用机制的深入洞察

L. as biofilm inhibitor: Insights into the mechanism of action using proteomics/metabolomics and toxicity studies.

作者信息

Gerschler Sandy, Maaß Sandra, Gerth Philip, Schulig Lukas, Wildgrube Toni, Rockstroh Jan, Wurster Martina, Methling Karen, Becher Dörte, Lalk Michael, Schulze Christian, Guenther Sebastian, Schultze Nadin

机构信息

Institute of Pharmacy, University of Greifswald, Friedrich-Ludwig-Jahn-Straße 17, 17489, Greifswald, Germany.

Institute of Microbiology, University of Greifswald, Felix-Hausdorff-Straße 8, 17489, Greifswald, Germany.

出版信息

Biofilm. 2025 Feb 28;9:100268. doi: 10.1016/j.bioflm.2025.100268. eCollection 2025 Jun.

Abstract

The successful sustainable cultivation of the well-known medicinal plant sundew on rewetted peatlands not only leads to the preservation of natural populations, but also provides a basis for the sustainable pharmaceutical use of the plant. The bioactive compounds of sundew, flavonoids and naphthoquinones, show biofilm-inhibiting properties against multidrug-resistant, ESBL-producing strains and open up new therapeutic possibilities. This study investigates the molecular mechanisms of these compounds in biofilm inhibition through proteomic analyses. Specific fractions of flavonoids and naphthoquinones, as well as individual substances like 7-methyljuglone and 2″--galloylhyperoside, are analyzed. Results show that naphthoquinones appear to act via central regulatory proteins such as OmpR and alter the stress response while flavonoids likely affect biofilm formation by creating an iron-poor environment through iron complexation and additionally influence polyamine balance, reducing intracellular spermidine levels. Further investigations including assays for iron complexation and analysis of polyamines confirmed the proteomic data. Safety evaluations through cytotoxicity tests in 3D cell cultures and the model confirm the safety of the extracts used. These findings highlight sundew as a promising candidate for new phytopharmaceuticals.

摘要

在重新湿润的泥炭地上成功可持续种植著名药用植物茅膏菜,不仅有助于保护自然种群,还为该植物的可持续药用提供了基础。茅膏菜的生物活性化合物,即黄酮类化合物和萘醌,对多重耐药、产超广谱β-内酰胺酶(ESBL)菌株具有生物膜抑制特性,并开辟了新的治疗可能性。本研究通过蛋白质组学分析探究这些化合物在生物膜抑制中的分子机制。对黄酮类化合物和萘醌的特定馏分以及7-甲基胡桃醌和2″-没食子酰基金丝桃苷等个别物质进行了分析。结果表明,萘醌似乎通过OmpR等中心调节蛋白发挥作用,并改变应激反应,而黄酮类化合物可能通过铁络合创造缺铁环境来影响生物膜形成,并额外影响多胺平衡,降低细胞内亚精胺水平。包括铁络合测定和多胺分析在内的进一步研究证实了蛋白质组学数据。通过3D细胞培养和模型中的细胞毒性试验进行的安全性评估证实了所用提取物的安全性。这些发现突出了茅膏菜作为新型植物药的有前景的候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c353/11930149/9b924117b61d/gr1.jpg

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