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发酵乳杆菌可减轻结扎诱导的牙周炎小鼠的牙槽骨丢失。

Lactobacillus fermentum attenuates the alveolar bone loss in ligature-induced periodontitis in mice.

机构信息

Department of Periodontology and Research Institute of Oral Sciences, Gangneung-Wonju National University College of Dentistry, Gangneung, Republic of Korea.

Department of Anatomy and Research Institute of Oral Sciences, Gangneung-Wonju National University College of Dentistry, Gangneung, Republic of Korea.

出版信息

Oral Dis. 2024 Jul;30(5):3328-3335. doi: 10.1111/odi.14739. Epub 2023 Sep 19.

DOI:10.1111/odi.14739
PMID:37724481
Abstract

OBJECTIVE

This study investigated the effects of Lactobacillus fermentum BELF11 on periodontitis in mice (LIP).

METHODS

Sixty mice were randomly assigned to a control group (CTL), LIP/PBS group (LIP and PBS applied), or LIP/BELF11 group (LIP and L. fermentum BELF11 applied). For 14 days, PBS or L. fermentum BELF11 was applied twice daily to the mice in the LIP/PBS or LIP/BELF11 group, respectively. After 14 days, radiographic, histological, and pro-inflammatory cytokine assessments were conducted.

RESULTS

The LIP/PBS and LIP/BELF11 groups demonstrated greater alveolar bone loss than the CTL group (p < 0.05). The LIP/BELF11 group showed significantly reduced alveolar bone loss on the mesial side compared to the LIP/PBS group. Histologically, the LIP/BELF11 group showed consistent patterns of connective tissue fiber arrangement, lower levels of inflammatory infiltration, less alveolar bone loss, and higher alveolar bone density than the LIP/PBS group, despite showing more signs of destruction than the CTL group. The LIP/BELF11 group also exhibited significantly lower levels of pro-inflammatory cytokines than the LIP/PBS group.

CONCLUSIONS

L. fermentum BELF11 inhibits alveolar bone loss and periodontitis progression by regulating pro-inflammatory cytokine production. These findings suggest that L. fermentum BELF11 may be a potential adjunctive therapy in periodontal treatment.

摘要

目的

本研究旨在探讨发酵乳杆菌 BELF11 对小鼠牙周炎(LIP)的影响。

方法

将 60 只小鼠随机分为对照组(CTL)、LIP/PBS 组(LIP 和 PBS 处理)和 LIP/BELF11 组(LIP 和 L. fermentum BELF11 处理)。LIP/PBS 组和 LIP/BELF11 组小鼠分别每天接受两次 PBS 或 L. fermentum BELF11 处理,持续 14 天。14 天后,对小鼠进行放射学、组织学和促炎细胞因子评估。

结果

与 CTL 组相比,LIP/PBS 组和 LIP/BELF11 组的牙槽骨丧失更为明显(p<0.05)。与 LIP/PBS 组相比,LIP/BELF11 组的近中侧牙槽骨丧失明显减少。组织学上,LIP/BELF11 组与 LIP/PBS 组相比,具有更一致的结缔组织纤维排列模式、更低水平的炎症浸润、较少的牙槽骨丧失和更高的牙槽骨密度,但与 CTL 组相比,仍显示出更多的破坏迹象。与 LIP/PBS 组相比,LIP/BELF11 组促炎细胞因子水平也显著降低。

结论

L. fermentum BELF11 通过调节促炎细胞因子的产生,抑制牙槽骨丧失和牙周炎的进展。这些发现表明,L. fermentum BELF11 可能是牙周治疗的一种潜在辅助治疗方法。

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