Department of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology & Metabolism, Medical University, Innsbruck, Austria.
Department of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology & Metabolism, Medical University, Innsbruck, Austria.
Cell Metab. 2022 Nov 1;34(11):1700-1718. doi: 10.1016/j.cmet.2022.09.017. Epub 2022 Oct 7.
Bidirectional crosstalk along the gut-liver axis controls gastrointestinal health and disease and exploits environmental and host mediators. Nutrients, microbial antigens, metabolites, and bile acids regulate metabolism and immune responses in the gut and liver, which reciprocally shape microbial community structure and function. Perturbation of such host-microbe interactions is observed in a variety of experimental liver diseases and is facilitated by an impaired intestinal barrier, which is fueling hepatic inflammation and disease progression. Clinical evidence describes perturbation of the gut-liver crosstalk in non-alcoholic fatty liver disease, alcoholic liver disease, and primary sclerosing cholangitis. In liver cirrhosis, a common sequela of these diseases, the intestinal microbiota and microbial pathogen-associated molecular patterns constitute liver inflammation and clinical complications, such as hepatic encephalopathy. Understanding the intricate metabolic interplay between the gut and liver in health and disease opens an avenue for targeted therapies in the future, which is probed in controlled clinical trials.
双向串扰沿着肠道-肝脏轴控制胃肠道健康和疾病,并利用环境和宿主介质。营养物质、微生物抗原、代谢物和胆汁酸调节肠道和肝脏的代谢和免疫反应,而肠道和肝脏反过来又塑造微生物群落的结构和功能。在各种实验性肝病中观察到这种宿主-微生物相互作用的破坏,并受到肠道屏障受损的促进,这加剧了肝炎症和疾病进展。临床证据描述了非酒精性脂肪性肝病、酒精性肝病和原发性硬化性胆管炎中肠道-肝脏串扰的破坏。在这些疾病的常见后遗症肝硬化中,肠道微生物群和微生物病原体相关分子模式构成了肝炎症和临床并发症,如肝性脑病。了解健康和疾病中肠道和肝脏之间复杂的代谢相互作用为未来的靶向治疗开辟了道路,这在对照临床试验中进行了探索。