法尼甾体X受体
熊去氧胆酸
脂肪肝
胆汁酸
微生物群
肠道菌群
毛螺菌科
硼胆酸
酒精性肝病
瘤胃球菌
医学
疾病
生物
肝硬化
厚壁菌
生物信息学
内科学
受体
免疫学
核受体
生物化学
兴奋剂
基因
转录因子
16S核糖体RNA
作者
Qingyi Mao,Beibei Lin,Wenluo Zhang,Yu Zhang,Yu Zhang,Qian Cao,Mengque Xu
标识
DOI:10.3389/fphar.2024.1371574
摘要
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease, resulting in a huge medical burden worldwide. Accumulating evidence suggests that the gut microbiome and bile acids play pivotal roles during the development of NAFLD. Patients with NAFLD exhibit unique signatures of the intestinal microbiome marked by the priority of Gram-negative bacteria, decreased ratio of Firmicutes/Bacteroidetes (F/B), and increased Prevotella and Lachnospiraceae . The intestinal microbiota is involved in the metabolism of bile acids. Ursodeoxycholic acid (UDCA) is a key determinant in maintaining the dynamic communication between the host and gut microbiota. It generally shows surprising therapeutic potential in NAFLD with several mechanisms, such as improving cellular autophagy, apoptosis, and mitochondrial functions. This action is based on its direct or indirect effect, targeting the farnesoid X receptor (FXR) and various other nuclear receptors. This review aims to discuss the current studies on the involvement of the microbiome–UDCA interface in NAFLD therapy and provide prospective insights into future preventative and therapeutic approaches for NAFLD.
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