Department of Physiology and Pathophysiology, Peking University Health Science Center, and Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing 100191, China.
Int J Mol Sci. 2020 Apr 26;21(9):3066. doi: 10.3390/ijms21093066.
Non-alcoholic fatty liver disease (NAFLD) is recognized as the most frequent classification of liver disease around the globe. Along with the sequencing technologies, gut microbiota has been regarded as a vital factor for the maintenance of human and animal health and the mediation of multiple diseases. The modulation of gut microbiota as a mechanism affecting the pathogenesis of NAFLD is becoming a growing area of concern. Recent advances in the communication between gut and hepatic tissue pave novel ways to better explain the molecular mechanisms regarding the pathological physiology of NAFLD. In this review, we recapitulate the current knowledge of the mechanisms correlated with the development and progression of NAFLD regulated by the gut microbiome and gut-liver axis, which may provide crucial therapeutic strategies for NAFLD. These mechanisms predominantly involve: (1) the alteration in gut microbiome profile; (2) the effects of components and metabolites from gut bacteria (e.g., lipopolysaccharides (LPS), trimethylamine-N-oxide (TMAO), and N,N,N-trimethyl-5-aminovaleric acid (TMAVA)); and (3) the impairment of intestinal barrier function and bile acid homeostasis. In particular, the prevention and therapy of NAFLD assisted by nutritional strategies are highlighted, including probiotics, functional oligosaccharides, dietary fibers, ω-3 polyunsaturated fatty acids, functional amino acids (L-tryptophan and L-glutamine), carotenoids, and polyphenols, based on the targets excavated from the gut-liver axis.
非酒精性脂肪性肝病 (NAFLD) 被认为是全球最常见的肝脏疾病分类。随着测序技术的发展,肠道微生物群已被认为是维持人类和动物健康以及介导多种疾病的重要因素。肠道微生物群的调节作为一种影响 NAFLD 发病机制的机制,正成为一个日益受到关注的领域。肠道和肝脏组织之间的交流的最新进展为更好地解释 NAFLD 的病理生理学的分子机制开辟了新的途径。在这篇综述中,我们总结了肠道微生物组和肠-肝轴调节与 NAFLD 发展和进展相关的机制的现有知识,这可能为 NAFLD 提供重要的治疗策略。这些机制主要涉及:(1)肠道微生物组谱的改变;(2)肠道细菌的成分和代谢物的影响(例如,脂多糖(LPS)、三甲胺 N-氧化物(TMAO)和 N,N,N-三甲基-5-氨基戊酸(TMAVA));(3)肠道屏障功能和胆汁酸稳态的损害。特别强调了基于从肠-肝轴挖掘的靶点,通过营养策略辅助预防和治疗 NAFLD,包括益生菌、功能性低聚糖、膳食纤维、ω-3 多不饱和脂肪酸、功能性氨基酸(L-色氨酸和 L-谷氨酰胺)、类胡萝卜素和多酚。