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原花色素抑制牙龈卟啉单胞菌及其葡糖基转移酶的生长和生物膜形成。

Inhibition of gingipains and Porphyromonas gingivalis growth and biofilm formation by prenyl flavonoids.

机构信息

Department of Life Science, Shokei University, Kumamoto, Japan.

Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

J Periodontal Res. 2017 Feb;52(1):89-96. doi: 10.1111/jre.12372. Epub 2016 Mar 9.

Abstract

BACKGROUND AND OBJECTIVE

Porphyromonas gingivalis is considered a major pathogen of chronic periodontitis, which also may be implicated with systemic diseases such as atherosclerosis. Secreted cysteine proteases, gingipains Rgp and Kgp, are essential for P. gingivalis virulence. Some polyphenols and flavonoids are known to inhibit gingipain activity and interfere with biofilm formation by P. gingivalis. Many bioactive compounds have been isolated from Epimedium species, but availability of these compounds on gingipains and P. gingivalis is still unclear. Therefore, the aim of this study was to evaluate natural products from medical plants to develop a new therapeutic agent against periodontal disease.

MATERIAL AND METHODS

Prenylated flavonoids were isolated from Epimedium species plant using column chromatographies. The inhibitory effect of the prenylated flavonoids against protease activity of gingipains were examined using purified gingipains and fluorogenic substrates. Anti-P. gingivalis activity was evaluated to analyze planktonic growth and biofilm formation in brain heart infusion medium in the presence of the prenylated flavonoids.

RESULTS

We isolated 17 prenylated flavonoids (Limonianin, Epimedokoreanin B, etc.) from Epimedium species. We found that some prenylated flavonoids inhibited gingipain activity in a non-competitive manner with K values at μm order. The prenylated flavonoids also hindered growth and biofilm formation of P. gingivalis, in a manner independent of gingipain inhibition by the compounds.

CONCLUSION

The results indicated an inhibitory effect of the prenylated flavonoids against P. gingivalis and would provide useful information for future development of periodontitis treatment that suppresses gingipains, P. gingivalis growth and biofilm formation.

摘要

背景与目的

牙龈卟啉单胞菌被认为是慢性牙周炎的主要病原体,它也可能与动脉粥样硬化等系统性疾病有关。分泌的半胱氨酸蛋白酶、Rgp 和 Kgp 牙龈蛋白酶对 P. gingivalis 的毒力至关重要。一些多酚和类黄酮已知能抑制牙龈蛋白酶的活性,并干扰 P. gingivalis 生物膜的形成。从淫羊藿属植物中分离出许多生物活性化合物,但这些化合物对牙龈蛋白酶和 P. gingivalis 的作用尚不清楚。因此,本研究旨在评估药用植物中的天然产物,以开发一种针对牙周病的新型治疗药物。

材料与方法

采用柱层析法从淫羊藿属植物中分离出苯丙素类黄酮。用纯化的牙龈蛋白酶和荧光底物检测苯丙素类黄酮对牙龈蛋白酶活性的抑制作用。分析苯丙素类黄酮对脑心浸液培养基中浮游生长和生物膜形成的抗 P. gingivalis 活性。

结果

从淫羊藿属植物中分离出 17 种苯丙素类黄酮(Limonianin、Epimedokoreanin B 等)。结果发现,一些苯丙素类黄酮以μm 级的 K 值以非竞争性方式抑制牙龈蛋白酶活性。苯丙素类黄酮还以不依赖于化合物抑制牙龈蛋白酶的方式,阻碍 P. gingivalis 的生长和生物膜形成。

结论

这些结果表明苯丙素类黄酮对 P. gingivalis 具有抑制作用,为未来开发抑制牙龈蛋白酶、P. gingivalis 生长和生物膜形成的牙周病治疗方法提供了有用信息。

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