Bile acid nuclear receptor FXR and digestive system diseases

Autor: Zhengtao Wang, Lili Ding, Wendong Huang, Li Yang
Jazyk: angličtina
Předmět:
BMI
body mass index

Review
G6Pase
glucose-6-phosphatase

Inflammatory bowel disease
HDL-C
high density lipoprotein cholesterol

SHP
small heterodimer partner

AOM
azoxymethane

AF2
activation domain

ERK
extracellular signal-regulated kinase

Gastrointestinal tract
GPBAR
G protein-coupled BA receptor

MRP2
multidrug resistance-associated protein 2

Glucose homeostasis
General Pharmacology
Toxicology and Pharmaceutics

OSTα
organic solute transporter alpha

BAAT
bile acid-CoA amino acid N-acetyltransferase

LCA
lithocholic acid

NF-κB
nuclear factor-kappa B

FGFR4
fibroblast growth factor receptor 4

CA
cholic acid

Bile acid
IBD
inflammatory bowel disease

HNF4α
hepatic nuclear factor 4α

Type 2 diabetes
TNFα
tumor necrosis factors α

I-BABP
intestinal bile acid-binding protein

FGF19
fibroblast growth factor 19

3. Good health
Cell biology
PEPCK
phosphoenol pyruvate carboxykinase

DSS
dextrane sodium sulfate

LPL
lipoprotein lipase

FFAs
free fatty acids

NOD
non-obese diabetic

AP-1
activator protein-1

GLUT2
glucose transporter type 2

medicine.medical_specialty
Cell signaling
LRH-1
liver receptor homolog-1

MCA
muricholicacid

medicine.drug_class
CREB
cAMP regulatory element-binding protein

SREBP-1c
sterol regulatory element-binding protein 1c

LBD
ligand binding domain

T2D
type 2 diabetes

Biology
Cholesterol 7 alpha-hydroxylase
UDCA
ursodeoxycholic acid

CDCA
chenodeoxycholic acid

FXR
farnesoid X receptor

VSG
vertical sleeve gastrectomy

Farnesoid X receptor
TNBS
trinitrobenzensulfonic acid

Internal medicine
FXRE
farnesoid X receptor response element

medicine
BAAT
GSK3
glycogen synthase kinase 3

KRAS
Kirsten rat sarcoma viral oncogene homolog

GLP-1
glucagon-like peptide 1

FABP6
fatty acid-binding protein subclass 6

BSEP
bile salt export pump

CD
Crohn׳s disease

ASBT
apical sodium-dependent bile salt transporter

PGC-1α
peroxisome proliferators-activated receptor γ coactivator protein-1α

BAs
bile acids

lcsh:RM1-950
FGF19
BACS
bile acid-CoA synthetase

STAT3
signal transducers and activators of transcription 3

CYP7A1
cholesterol 7α-hydroxylase

KLF11
Krüppel-like factor 11

Colorectal cancer
IL-1
interleukin 1

Bile acids
UC
ulcerative colitis

lcsh:Therapeutics. Pharmacology
Endocrinology
Nuclear receptor
Apo
apolipoprotein

DCA
deoxycholic acid

DBD
DNA binding domain

ANGTPL3
angiopoietin-like protein 3

db/db
diabetic mice

TLCA
taurolithocholic acid

GPCRs
G protein-coupled receptors

NRs
nuclear receptors

OSTβ
organic solute transporter beta

6-ECDCA
6α-ethyl-chenodeoxycholic acid
Zdroj: Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica B, Vol 5, Iss 2, Pp 135-144 (2015)
ISSN: 2211-3835
DOI: 10.1016/j.apsb.2015.01.004
Popis: Bile acids (BAs) are not only digestive surfactants but also important cell signaling molecules, which stimulate several signaling pathways to regulate some important biological processes. The bile-acid-activated nuclear receptor, farnesoid X receptor (FXR), plays a pivotal role in regulating bile acid, lipid and glucose homeostasis as well as in regulating the inflammatory responses, barrier function and prevention of bacterial translocation in the intestinal tract. As expected, FXR is involved in the pathophysiology of a wide range of diseases of gastrointestinal tract, including inflammatory bowel disease, colorectal cancer and type 2 diabetes. In this review, we discuss current knowledge of the roles of FXR in physiology of the digestive system and the related diseases. Better understanding of the roles of FXR in digestive system will accelerate the development of FXR ligands/modulators for the treatment of digestive system diseases.
Graphical abstract The bile-acid-activated nuclear receptor, farnesoid X receptor (FXR), is involved in the pathophysiology of a wide range of diseases of gastrointestinal tract, including inflammatory bowel disease, colorectal cancer and type 2 diabetes. In this review, authors discuss current knowledge of the roles of FXR in physiology of the digestive system and the related diseases.
Databáze: OpenAIRE