Wang Ting, Ishikawa Taichi, Sasaki Minoru, Chiba Toshimi
Division of Internal Medicine, Department of Oral Medicine, Iwate Medical University, Morioka, Japan.
Division of Molecular Microbiology, Department of Microbiology, Iwate Medical University, Morioka, Japan.
Front Med (Lausanne). 2022 Mar 2;9:822190. doi: 10.3389/fmed.2022.822190. eCollection 2022.
Gut microbiota play many important roles, such as the regulation of immunity and barrier function in the intestine, and are crucial for maintaining homeostasis in living organisms. The disruption in microbiota is called dysbiosis, which has been associated with various chronic inflammatory conditions, food allergies, colorectal cancer, etc. The gut microbiota is also affected by several other factors such as diet, antibiotics and other medications, or bacterial and viral infections. Moreover, there are some reports on the oral-gut-liver axis indicating that the disruption of oral microbiota affects the intestinal biota. Non-alcoholic fatty liver disease (NAFLD) is one of the systemic diseases caused due to the dysregulation of the oral-gut-liver axis. NAFLD is the most common liver disease reported in the developed countries. It includes liver damage ranging from simple steatosis to nonalcoholic steatohepatitis (NASH), cirrhosis, and cancer. Recently, accumulating evidence supports an association between NAFLD and dysbiosis of oral and gut microbiota. Periodontopathic bacteria, especially , have been correlated with the pathogenesis and development of NAFLD based on the clinical and basic research, and immunology. was detected in the liver, and lipopolysaccharide from this bacteria has been shown to be involved in the progression of NAFLD, thereby indicating a direct role of in NAFLD. Moreover, induces dysbiosis of gut microbiota, which promotes the progression of NAFLD, through disrupting both metabolic and immunologic pathways. Here, we review the roles of microbial dysbiosis in NAFLD. Focusing on , we evaluate and summarize the most recent advances in our understanding of the relationship between oral-gut microbiome symbiosis and the pathogenesis and progression of non-alcoholic fatty liver disease, as well as discuss novel strategies targeting both and microbial dysbiosis.
肠道微生物群发挥着许多重要作用,如调节肠道免疫和屏障功能,对维持生物体的内环境稳态至关重要。微生物群的破坏称为生态失调,这与各种慢性炎症性疾病、食物过敏、结直肠癌等有关。肠道微生物群还受到其他几个因素的影响,如饮食、抗生素和其他药物,或细菌和病毒感染。此外,有一些关于口-肠-肝轴的报道表明,口腔微生物群的破坏会影响肠道生物群。非酒精性脂肪性肝病(NAFLD)是由于口-肠-肝轴失调引起的全身性疾病之一。NAFLD是发达国家报道的最常见的肝脏疾病。它包括从单纯脂肪变性到非酒精性脂肪性肝炎(NASH)、肝硬化和癌症等肝脏损伤。最近,越来越多的证据支持NAFLD与口腔和肠道微生物群生态失调之间的关联。基于临床和基础研究以及免疫学,牙周病原菌,尤其是,已与NAFLD的发病机制和发展相关。在肝脏中检测到,并且已证明这种细菌的脂多糖参与了NAFLD的进展,从而表明在NAFLD中起直接作用。此外,通过破坏代谢和免疫途径,诱导肠道微生物群生态失调,促进NAFLD的进展。在这里,我们综述了微生物生态失调在NAFLD中的作用。聚焦于,我们评估并总结了我们对口腔-肠道微生物群共生与非酒精性脂肪性肝病的发病机制和进展之间关系的最新认识进展,并讨论了针对和微生物生态失调的新策略。