Chen Liuying, Zhu Yixin, Hou Xiaohua, Yang Ling, Chu Huikuan
Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Medicine, University of California, San Diego, San Diego, CA, United States.
Front Med (Lausanne). 2022 Mar 3;9:840752. doi: 10.3389/fmed.2022.840752. eCollection 2022.
Cirrhosis and liver cancer caused by alcohol-associated liver disease (ALD) are serious threats to people's health. In addition to hepatic cell apoptosis and liver inflammation caused by oxidative stress during alcohol metabolism, intestinal microbiota disorders are also involved in the onset and development of ALD. Ethanol and its' oxidative and non-oxidative metabolites, together with dysbiosis-caused-inflammation, destroys the intestinal barrier. Changes of several microbial metabolites, such as bile acids, short-chain fatty acids, and amino acid, are closely associated with gut dysbiosis in ALD. The alcohol-caused dysbiosis can further influence intestinal barrier-related proteins, such as mucin2, bile acid-related receptors, and aryl hydrocarbon receptor (AhR), and these abnormal changes also participate in the injury of the intestinal barrier and hepatic steatosis. Gut-derived bacteria, fungi, and their toxins, such as lipopolysaccharide (LPS) and β-glucan translocate into the liver through the damaged intestinal barrier and promote the progression of inflammation and fibrosis of ALD. Thus, the prevention of alcohol-induced disruption of intestinal permeability has a beneficial effect on ALD. Currently, multiple therapeutic treatments have been applied to restore the gut microbiota of patients with ALD. Fecal microbial transplantation, probiotics, antibiotics, and many other elements has already shown their ability of restoring the gut microbiota. Targeted approaches, such as using bacteriophages to remove cytolytic , and supplement with , or are also powerful therapeutic options for ALD.
酒精性肝病(ALD)所致的肝硬化和肝癌严重威胁着人们的健康。除了酒精代谢过程中氧化应激引起的肝细胞凋亡和肝脏炎症外,肠道微生物群紊乱也参与了ALD的发生和发展。乙醇及其氧化和非氧化代谢产物,连同菌群失调引起的炎症,破坏了肠道屏障。几种微生物代谢产物的变化,如胆汁酸、短链脂肪酸和氨基酸,与ALD中的肠道菌群失调密切相关。酒精引起的菌群失调可进一步影响肠道屏障相关蛋白,如粘蛋白2、胆汁酸相关受体和芳烃受体(AhR),这些异常变化也参与肠道屏障损伤和肝脂肪变性。肠道来源的细菌、真菌及其毒素,如脂多糖(LPS)和β-葡聚糖,通过受损的肠道屏障转移到肝脏,促进ALD炎症和纤维化的进展。因此,预防酒精引起的肠道通透性破坏对ALD有有益作用。目前,多种治疗方法已被应用于恢复ALD患者的肠道微生物群。粪便微生物移植、益生菌、抗生素等许多方法已显示出恢复肠道微生物群的能力。靶向方法,如使用噬菌体去除溶细胞性细菌,以及补充特定物质等,也是治疗ALD的有力选择。