Fujian Key Laboratory of Oral Diseases & Fujian Provincial Engineering Research Center of Oral Biomaterial & Stomatological Key laboratory of Fujian College and University, School and Hospital of Stomatology, Fujian Medical University, Fuzhou, P.R. China.
Institute of Stomatology & Laboratory of Oral Tissue Engineering, School and Hospital of Stomatology, Fujian Medical University, Fuzhou, 350002, P.R. China.
J Neuroinflammation. 2024 Oct 18;21(1):263. doi: 10.1186/s12974-024-03256-8.
Periodontitis exacerbates Alzheimer's disease (AD) through multiple pathways. Both periodontitis and AD are intricately correlated to intestinal homeostasis, yet there is still a lack of direct evidence regarding whether periodontitis can regulate the progression of AD by modulating intestinal homeostasis. The current study induced experimental periodontitis in AD mice by bilaterally ligating the maxillary second molars with silk and administering Pg-LPS injections in APP/PS1 (APP/PS1) mice. Behavioral tests and histological analyses of brain tissue were conducted after 8 weeks. Gut microbiota was analyzed and colon tissue were also evaluated. Then, fecal microbiota from mice with periodontitis was transplanted into antibiotic-treated mice to confirm the effects of periodontitis on AD and the potential mechanism was explored. The results indicated periodontitis exacerbated cognitive impairment and anxious behaviour in APP/PS1 mice, with increased Aβ deposition, microglial overactivation and neuroinflammation in brain. Moreover, the intestinal homeostasis of AD mice was altered by periodontitis, including affecting gut microbiota composition, causing colon inflammation and destroyed intestinal epithelial barrier. Furthermore, AD mice that underwent fecal transplantation from mice with periodontitis exhibited worsened AD progression and disrupted intestinal homeostasis. It also impaired intestinal barrier function, elevated peripheral inflammation, damaged blood-brain barrier (BBB) and caused neuroinflammation and synapses impairment. Taken together, the current study demonstrated that periodontitis could disrupt intestinal homeostasis to exacerbate AD progression potential via causing gut microbial dysbiosis, intestinal inflammation and intestinal barrier impairment to induce peripheral inflammation and damage BBB, ultimately leading to neuroinflammation and synapse impairment. It underscores the importance of maintaining both periodontal health and intestinal homeostasis to reduce the risk of AD.
牙周炎通过多种途径加重阿尔茨海默病(AD)。牙周炎和 AD 都与肠道内环境密切相关,但目前仍缺乏牙周炎是否可以通过调节肠道内环境来控制 AD 进展的确切证据。本研究通过丝线结扎上颌第二磨牙在 APP/PS1(APP/PS1)小鼠中诱导实验性牙周炎,并给予 Pg-LPS 注射。8 周后进行行为测试和脑组织组织学分析。分析肠道微生物群,并评估结肠组织。然后,将牙周炎小鼠的粪便微生物群移植到接受抗生素治疗的小鼠中,以确认牙周炎对 AD 的影响,并探讨潜在的机制。结果表明,牙周炎加重了 APP/PS1 小鼠的认知障碍和焦虑行为,导致大脑中 Aβ 沉积增加、小胶质细胞过度激活和神经炎症。此外,牙周炎改变了 AD 小鼠的肠道内环境,包括影响肠道微生物群组成、引起结肠炎症和破坏肠道上皮屏障。此外,接受来自牙周炎小鼠粪便移植的 AD 小鼠表现出 AD 进展恶化和肠道内环境破坏。它还损害了肠道屏障功能,增加了外周炎症,破坏了血脑屏障(BBB),并导致神经炎症和突触损伤。总之,本研究表明,牙周炎可能通过引起肠道微生物失调、肠道炎症和肠道屏障损伤来破坏肠道内环境,从而加重 AD 进展的潜力,导致外周炎症和 BBB 损伤,最终导致神经炎症和突触损伤。这强调了保持牙周健康和肠道内环境稳定以降低 AD 风险的重要性。