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卡瓦-241 减少了胶原抗体引发的伴放线放线杆菌牙周炎模型中的牙周破坏。

Kava-241 reduced periodontal destruction in a collagen antibody primed Porphyromonas gingivalis model of periodontitis.

机构信息

Henry M.Goldman School of Dental Medicine, Boston University, Boston, MA, USA.

Department of Chemistry, Boston University, Boston, MA, USA.

出版信息

J Clin Periodontol. 2017 Nov;44(11):1123-1132. doi: 10.1111/jcpe.12784. Epub 2017 Sep 21.

Abstract

AIM

The aim of this study was to evaluate the effect of Kava-241, an optimized Piper methysticum Kava compound, on periodontal destruction in a collagen antibody primed oral gavage model of periodontitis.

METHODS

Experimental periodontitis was induced by oral gavage of Porphyromonas gingivalis (P. gingivalis) + type II collagen antibody (AB) in mice during 15 days. Mice were treated with Kava-241 concomitantly or prior to P. gingivalis gavage and compared to untreated mice. Comprehensive histomorphometric analyses were performed.

RESULTS

Oral gavage with P. gingivalis induced mild epithelial down-growth and alveolar bone loss, while oral gavage with additional AB priming had greater tissular destruction in comparison with gavage alone (p < .05). Kava-241 treatment significantly (p < .05) reduced epithelial down-growth (72%) and alveolar bone loss (36%) in P. gingivalis+AB group. This Kava-241 effect was associated to a reduction in inflammatory cell counts within soft tissues and an increase in fibroblasts (p < .05).

CONCLUSION

Priming with type II collagen antibody with oral gavage is a fast and reproducible model of periodontal destruction adequate for the evaluation of novel therapeutics. The effect of Kava-241 shows promise in the prevention and treatment of inflammation and alveolar bone loss associated with periodontitis. Further experiments are required to determine molecular pathways targeted by this therapeutic agent.

摘要

目的

本研究旨在评估优化的胡椒基 methysticum Kava 化合物 Kava-241 对胶原抗体诱导的牙周炎口腔灌胃模型中牙周破坏的影响。

方法

通过口腔灌胃牙龈卟啉单胞菌(P. gingivalis)+II 型胶原抗体(AB)在小鼠中诱导实验性牙周炎,持续 15 天。在 P. gingivalis 灌胃前或同时给予 Kava-241 治疗,并与未治疗的小鼠进行比较。进行全面的组织形态计量学分析。

结果

口腔灌胃 P. gingivalis 可引起轻微的上皮向下生长和牙槽骨丧失,而额外的 AB 预灌胃可引起比单独灌胃更大的组织破坏(p<.05)。Kava-241 治疗可显著降低 P. gingivalis+AB 组的上皮向下生长(72%)和牙槽骨丧失(36%)(p<.05)。这种 Kava-241 作用与软组织中炎症细胞计数减少和成纤维细胞增加有关(p<.05)。

结论

口腔灌胃 II 型胶原抗体预刺激是一种快速且可重复的牙周破坏模型,适用于评估新型治疗方法。Kava-241 的作用有望预防和治疗与牙周炎相关的炎症和牙槽骨丧失。需要进一步的实验来确定这种治疗剂靶向的分子途径。

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