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乳酸链球菌素与甘草多酚的生物相容性组合对粪肠球菌具有协同杀菌作用,并抑制单核细胞中的NF-κB活化。

Biocompatible combinations of nisin and licorice polyphenols exert synergistic bactericidal effects against Enterococcus faecalis and inhibit NF-κB activation in monocytes.

作者信息

Grenier Daniel, Marcoux Eve, Azelmat Jabrane, Ben Lagha Amel, Gauthier Philippe

机构信息

Oral Ecology Research Group, Faculty of Dentistry, Université Laval, 2420 de la Terrasse, Quebec City, QC, G1V 0A6, Canada.

出版信息

AMB Express. 2020 Jul 6;10(1):120. doi: 10.1186/s13568-020-01056-w.

Abstract

Enterococcus faecalis is one of the bacterial species most frequently isolated from persistent endodontic and apical periodontal infections. The aim of the present study was to evaluate the synergistic antibacterial effects of nisin and selected licorice polyphenols (glabridin, licoricidin, licochalcone A) against planktonic and biofilm-embedded E. faecalis cells. The biocompatibility and anti-inflammatory properties of the nisin/licorice polyphenol combinations were also investigated. The lantibiotic bacteriocin (nisin), the two isoflavonoids (glabridin, licoricidin), and the chalcone (licochalcone A) efficiently inhibited the growth of E. faecalis, with MICs ranging from 6.25 to 25 µg/mL. Combining nisin with each licorice polyphenol individually resulted in a significant synergistic antibacterial effect. Following a 30-min contact, nisin in combination with either glabridin, licoricidin, or licochalcone A caused significant biofilm killing. The nisin/licorice polyphenol combinations had no cytotoxic effects (oral epithelial cells, gingival fibroblasts, and stem cells of the apical papilla), with the exception of nisin/glabridin, when used at their MICs. Lastly, we showed that nisin/glabridin, nisin/licoricidin, and nisin/licochalcone A inhibit NF-κB activation induced by E. faecalis in a monocyte model, suggesting that these combinations possess anti-inflammatory properties. The present study provides evidence that combinations of nisin and glabridin, licoricidin, or licochalcone A show promise as root canal disinfection agents.

摘要

粪肠球菌是最常从持续性牙髓和根尖周牙周感染中分离出的细菌种类之一。本研究的目的是评估乳酸链球菌素和选定的甘草多酚(光甘草定、甘草杀菌素、甘草查尔酮A)对浮游和生物膜包被的粪肠球菌细胞的协同抗菌作用。还研究了乳酸链球菌素/甘草多酚组合的生物相容性和抗炎特性。羊毛硫抗生素细菌素(乳酸链球菌素)、两种异黄酮(光甘草定、甘草杀菌素)和查尔酮(甘草查尔酮A)有效地抑制了粪肠球菌的生长,最低抑菌浓度范围为6.25至25μg/mL。将乳酸链球菌素分别与每种甘草多酚联合使用产生了显著的协同抗菌效果。接触30分钟后,乳酸链球菌素与光甘草定、甘草杀菌素或甘草查尔酮A联合使用可显著杀灭生物膜。除了在最低抑菌浓度下使用时的乳酸链球菌素/光甘草定组合外,乳酸链球菌素/甘草多酚组合对(口腔上皮细胞、牙龈成纤维细胞和根尖乳头干细胞)没有细胞毒性作用。最后,我们表明,在单核细胞模型中,乳酸链球菌素/光甘草定、乳酸链球菌素/甘草杀菌素和乳酸链球菌素/甘草查尔酮A可抑制粪肠球菌诱导的核因子κB激活,这表明这些组合具有抗炎特性。本研究提供了证据,表明乳酸链球菌素与光甘草定、甘草杀菌素或甘草查尔酮A的组合有望作为根管消毒剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cee/7338318/d1fe8e13974b/13568_2020_1056_Fig1_HTML.jpg

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