TY - JOUR
T1 - Bile acids
T2 - emerging role in management of liver diseases
AU - Asgharpour, Amon
AU - Kumar, Divya
AU - Sanyal, Arun
N1 - Publisher Copyright:
© 2015, Asian Pacific Association for the Study of the Liver.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - Bile acids are well known for their effects on cholesterol homeostasis and lipid digestion. Since the discovery of bile acid receptors, of which there are farnesoid X receptor (FXR), a nuclear receptor, and the plasma membrane G-protein receptor, as well as Takeda G-protein coupled receptor clone 5, further roles have been elucidated for bile acids including glucose and lipid metabolism as well as inflammation. Additionally, treatment with bile acid receptor agonists has shown a decrease in the amount of atherosclerosis plaque formation and decreased portal vascular resistance and portal hypotension in animal models. Furthermore, rodent models have demonstrated antifibrotic activity using bile acid receptor agonists. Early human data using a FXR agonist, obeticholic acid, have shown promising results with improvement of histological activity and even a reduction of fibrosis. Human studies are ongoing and will provide further information on bile acid receptor agonist therapies. Thus, bile acids and their derivatives have the potential for management of liver diseases and potentially other disease states including diabetes and the metabolic syndrome.
AB - Bile acids are well known for their effects on cholesterol homeostasis and lipid digestion. Since the discovery of bile acid receptors, of which there are farnesoid X receptor (FXR), a nuclear receptor, and the plasma membrane G-protein receptor, as well as Takeda G-protein coupled receptor clone 5, further roles have been elucidated for bile acids including glucose and lipid metabolism as well as inflammation. Additionally, treatment with bile acid receptor agonists has shown a decrease in the amount of atherosclerosis plaque formation and decreased portal vascular resistance and portal hypotension in animal models. Furthermore, rodent models have demonstrated antifibrotic activity using bile acid receptor agonists. Early human data using a FXR agonist, obeticholic acid, have shown promising results with improvement of histological activity and even a reduction of fibrosis. Human studies are ongoing and will provide further information on bile acid receptor agonist therapies. Thus, bile acids and their derivatives have the potential for management of liver diseases and potentially other disease states including diabetes and the metabolic syndrome.
KW - Bile acids
KW - FXR
KW - Liver disease
KW - TGR5
UR - https://www.scopus.com/pages/publications/84944516583
U2 - 10.1007/s12072-015-9656-7
DO - 10.1007/s12072-015-9656-7
M3 - Review article
C2 - 26320013
AN - SCOPUS:84944516583
SN - 1936-0533
VL - 9
SP - 527
EP - 533
JO - Hepatology International
JF - Hepatology International
IS - 4
ER -