Farnesoid X Receptor Agonists: A Promising Therapeutic Strategy for Gastrointestinal Diseases

被引:12
作者
Almeqdadi, Mohammad [1 ]
Gordon, Fredric D. [2 ]
机构
[1] Lahey Hosp & Med Ctr, Div Transplantat & Hepatobiliary Dis, Burlington, MA USA
[2] Tufts Med Ctr, Abdominal Transplant Inst, 800 Washington St,4 South, Boston, MA 02111 USA
来源
GASTRO HEP ADVANCES | 2024年 / 3卷 / 03期
关键词
FXR Agonists; Liver Disease; Bile Acids; Metabolic Effects; Immunomodulatory Effects; OBETICHOLIC ACID; NONALCOHOLIC STEATOHEPATITIS; NUCLEAR RECEPTOR; INDUCED AUTOPHAGY; LIVER; FXR; ETHANOL; TRANSPORTER; MULTICENTER; MICROBIOME;
D O I
10.1016/j.gastha.2023.09.013
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Farnesoid X receptor (FXR) agonists have emerged as a promising therapeutic strategy for the management of various gastrointestinal (GI) diseases, including primary biliary cholangitis, nonalcoholic fatty liver disease, inflammatory bowel disease, alcohol-related liver disease, and primary sclerosing cholangitis. In this review, we discuss the mechanisms of action of FXR agonists, including their metabolic and immunomodulatory effects, and provide an overview of the clinical evidence supporting their use in the treatment of GI diseases. We also highlight the safety, adverse effects, and potential drug interactions associated with FXR agonists. While these agents have demonstrated efficacy in improving liver function, reducing hepatic steatosis, and improving histological endpoints in primary biliary cholangitis and nonalcoholic fatty liver disease, further research is needed to determine their long-term safety and effectiveness in other GI diseases, such as inflammatory bowel disease, alcohol-related liver disease, and primary sclerosing cholangitis. Additionally, the development of next-generation FXR agonists with improved potency and reduced side effects could further enhance their therapeutic potential.
引用
收藏
页码:344 / 352
页数:9
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