Department of Pharmacology, Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, PR China; Department of Pharmacy, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang 441021, China.
Department of Pharmacology, Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, PR China.
Exp Neurol. 2020 Apr;326:113176. doi: 10.1016/j.expneurol.2020.113176. Epub 2020 Jan 8.
Epidemiological studies suggest that chronic periodontitis (CP) is closely associated with the incidence and progression of cognitive impairment. The present study investigated the causal relationship between CP and cognitive decline and the underlying mechanism in mice. Long-term ligature around the left second maxillary molar tooth was used to induce CP in mice. Severe alveolar bone loss and inflammatory changes were observed in gingival tissues, accompanied by progressive cognitive deficits during a 12-month period. We also observed cerebral neuronal and synaptic injury and glial activation in this mouse model of CP. Furthermore, CP mice exhibited significant dysbiosis of the oral and gut microbiota, disruption of the intestinal barrier and blood-brain barrier, increases in the serum contents of proinflammatory cytokines and lipopolysaccharide (LPS), and increases in brain LPS levels, Toll-like receptor 4 (TLR4) expression, nuclear factor-κB (NF-κB) nuclear translocation and proinflammatory cytokine mRNA levels. These results indicate that CP may directly induce progressive cognitive decline and its mechanism is probably related to microbiota-gut-brain axis disorders, LPS/TLR4/NF-κB signaling activation and neuroinflammatory responses in mice. Therefore, the microbiota-gut-brain axis may provide the potential strategy for the prevention and treatment of CP-associated cognitive impairment.
流行病学研究表明,慢性牙周炎(CP)与认知障碍的发生和进展密切相关。本研究旨在探讨 CP 与认知能力下降之间的因果关系及其在小鼠中的潜在机制。通过结扎左侧上颌第二磨牙来诱导 CP 发生在小鼠中。在长达 12 个月的时间里,我们观察到牙龈组织中出现严重的牙槽骨丧失和炎症改变,同时伴有进行性认知缺陷。我们还观察到 CP 小鼠的大脑神经元和突触损伤以及神经胶质细胞激活。此外,CP 小鼠的口腔和肠道微生物群发生显著失调,肠道屏障和血脑屏障被破坏,促炎细胞因子和脂多糖(LPS)的血清含量增加,大脑 LPS 水平、Toll 样受体 4(TLR4)表达、核因子-κB(NF-κB)核易位以及促炎细胞因子 mRNA 水平升高。这些结果表明 CP 可能直接导致进行性认知能力下降,其机制可能与微生物群-肠道-大脑轴紊乱、LPS/TLR4/NF-κB 信号通路激活和神经炎症反应有关。因此,微生物群-肠道-大脑轴可能为预防和治疗 CP 相关的认知障碍提供潜在策略。