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牙周炎相关唾液微生物群通过肠脑轴相互作用加重阿尔茨海默病。

Periodontitis-related salivary microbiota aggravates Alzheimer's disease via gut-brain axis crosstalk.

机构信息

Nanjing Stomatological Hospital, Medical School of Nanjing University, Nanjing, China.

出版信息

Gut Microbes. 2022 Jan-Dec;14(1):2126272. doi: 10.1080/19490976.2022.2126272.

Abstract

The oral cavity is the initial chamber of digestive tract; the saliva swallowed daily contains an estimated 1.5 × 10 oral bacteria. Increasing evidence indicates that periodontal pathogens and subsequent inflammatory responses to them contribute to the pathogenesis of Alzheimer's disease (AD). The intestine and central nervous system jointly engage in crosstalk; microbiota-mediated immunity significantly impacts AD via the gut-brain axis. However, the exact mechanism linking periodontitis to AD remains unclear. In this study, we explored the influence of periodontitis-related salivary microbiota on AD based on the gut-brain crosstalk in APP/PS1 (PAP) transgenic mice. Saliva samples were collected from patients with periodontitis and healthy individuals. The salivary microbiota was gavaged into PAP mice for two months. Continuous gavage of periodontitis-related salivary microbiota in PAP mice impaired cognitive function and increased β-amyloid accumulation and neuroinflammation. Moreover, these AD-related pathologies were consistent with gut microbial dysbiosis, intestinal pro-inflammatory responses, intestinal barrier impairment, and subsequent exacerbation of systemic inflammation, suggesting that the periodontitis-related salivary microbiota may aggravate AD pathogenesis through crosstalk of the gut-brain axis. In this study, we demonstrated that periodontitis might participate in the pathogenesis of AD by swallowing salivary microbiota, verifying the role of periodontitis in AD progression and providing a novel perspective on the etiology and intervention strategies of AD.

摘要

口腔是消化道的初始腔室;每天吞咽的唾液中估计含有 1.5×10 口腔细菌。越来越多的证据表明,牙周病原体及其随后的炎症反应有助于阿尔茨海默病(AD)的发病机制。肠道和中枢神经系统共同参与串扰;通过肠-脑轴,微生物群介导的免疫对 AD 有重大影响。然而,将牙周炎与 AD 联系起来的确切机制尚不清楚。在这项研究中,我们基于 APP/PS1(PAP)转基因小鼠的肠-脑串扰,探讨了牙周炎相关唾液微生物群对 AD 的影响。从牙周炎患者和健康个体中采集唾液样本。将唾液微生物群灌胃 PAP 小鼠两个月。持续灌胃牙周炎相关唾液微生物群会损害 PAP 小鼠的认知功能,增加β-淀粉样蛋白积累和神经炎症。此外,这些与 AD 相关的病理学与肠道微生物失调、肠道促炎反应、肠道屏障损伤以及随后的全身炎症加剧一致,表明牙周炎相关唾液微生物群可能通过肠-脑轴的串扰加重 AD 的发病机制。在这项研究中,我们证明了牙周炎可能通过吞咽唾液微生物群参与 AD 的发病机制,验证了牙周炎在 AD 进展中的作用,并为 AD 的病因和干预策略提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a6c/9542625/c8011ec34da6/KGMI_A_2126272_F0001_OC.jpg

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