NR1H4 and atherosclerosis: In atherosclerosis mice model induced by high fat/cholesterol diet, geniposide expedited reversal cholesterol transport, motivated bile acid synthesis and excretion, and attenuated atherosclerosis inflammatory injury by modulating FXR-mediated bile acids liver-gut crosstalk and miR-101/MKP-1/p38 signaling pathways [89, 90].