Han Hui, Jiang Yi, Wang Mengyu, Melaku Mebratu, Liu Lei, Zhao Yong, Everaert Nadia, Yi Bao, Zhang Hongfu
State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Precision Livestock and Nutrition Unit, Gembloux Agro-Bio Tech, University of Liège, Gembloux, Belgium.
Crit Rev Food Sci Nutr. 2023;63(12):1689-1706. doi: 10.1080/10408398.2021.1966738. Epub 2021 Aug 18.
Nonalcoholic fatty liver disease (NAFLD) is one of the most common chronic liver disorders in humans, partly because it is closely related to metabolic disorders of the liver with increasing prevalence. NAFLD begins with hepatic lipid accumulation, which may cause inflammation and eventually lead to fibrosis in the liver. Numerous studies have demonstrated the close relationship between gut dysfunction (especially the gut microbiota and its metabolites) and the occurrence and progression of NAFLD. The bidirectional communication between the gut and liver, named the gut-liver axis, is mainly mediated by the metabolites derived from both the liver and gut through the biliary tract, portal vein, and systemic circulation. Herein, we review the effects of the gut-liver axis on the pathogenesis of NAFLD. We also comprehensively describe the potential molecular mechanisms from the perspective of the role of liver-derived metabolites and gut-related components in hepatic metabolism and inflammation and gut health, respectively. The study provides insights into the mechanisms underlying current summarizations that support the intricate interactions between a disordered gut and NAFLD and can provide novel strategies to lessen the prevalence and consequence of NAFLD.
非酒精性脂肪性肝病(NAFLD)是人类最常见的慢性肝脏疾病之一,部分原因是它与肝脏代谢紊乱密切相关且患病率不断上升。NAFLD始于肝脏脂质蓄积,这可能会引发炎症并最终导致肝脏纤维化。大量研究表明肠道功能障碍(尤其是肠道微生物群及其代谢产物)与NAFLD的发生和发展密切相关。肠道与肝脏之间的双向交流,即肠-肝轴,主要由肝脏和肠道通过胆道、门静脉和体循环产生的代谢产物介导。在此,我们综述了肠-肝轴对NAFLD发病机制的影响。我们还分别从肝脏衍生代谢产物和肠道相关成分在肝脏代谢、炎症以及肠道健康中的作用角度,全面描述了潜在的分子机制。该研究为当前支持紊乱肠道与NAFLD之间复杂相互作用的总结背后的机制提供了见解,并可为降低NAFLD的患病率和后果提供新策略。