Document Detail

Bile alcohols function as the ligands of membrane-type bile acid-activated G protein-coupled receptor.
MedLine Citation:
PMID:  20023205     Owner:  NLM     Status:  MEDLINE    
TGR5 is a G protein-coupled receptor that is activated by bile acids, resulting in an increase in cAMP levels and the subsequent modulation of energy expenditure in brown adipose tissue and muscle. Therefore, the development of a TGR5-specific agonist could lead to the prevention and treatment of various metabolic disorders related to obesity. In the present study, we evaluated the ability of bile alcohols, which are structurally and physiologically similar to bile acids and are produced as the end products of cholesterol catabolism in evolutionarily primitive vertebrates, to act as TGR5 agonists. In a cell-based reporter assay and a cAMP production assay performed in vitro, most bile alcohols with a side chain containing hydroxyl group(s) were highly efficacious agonists for TGR5 comparable to its most potent ligand in the naturally occurring bile acid, lithocholic acid. However, the abilities of the bile alcohols to activate TGR5 varied with the position and number of the hydroxyl substituent in the side chain. Additionally, the conformation of the steroidal nucleus of bile alcohols is also important for its activity as a TGR5 agonist. Thus, we have provided new insights into the structure-activity relationships of bile alcohols as TGR5 agonists.
Yusuke Iguchi; Masafumi Yamaguchi; Hiroyuki Sato; Kenji Kihira; Tomoko Nishimaki-Mogami; Mizuho Une
Related Documents :
8064365 - Dietary psyllium hydrocolloid and pectin increase bile acid pool size and change bile a...
10203155 - Profile of urinary bile acids in infants and children: developmental pattern of excreti...
8938185 - Stimulation of bile acid independent bile flow with bromo-cyclic guanosine monophosphate.
2365985 - The role of calcium precipitation in the sulfoglycolithocholate-induced cholestasis of ...
9053555 - Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas...
2820885 - Effect of a fish-oil-supplemented diet on inflammation and immunological processes in r...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-12-18
Journal Detail:
Title:  Journal of lipid research     Volume:  51     ISSN:  0022-2275     ISO Abbreviation:  J. Lipid Res.     Publication Date:  2010 Jun 
Date Detail:
Created Date:  2010-05-12     Completed Date:  2010-08-17     Revised Date:  2011-07-28    
Medline Journal Info:
Nlm Unique ID:  0376606     Medline TA:  J Lipid Res     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1432-41     Citation Subset:  IM    
Laboratory of Organic and Bio-molecular Chemistry, Faculty of Pharmaceutical Science, Hiroshima International University, Kure, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cell Line
Cell Membrane / metabolism*
Cholestanols / chemistry,  metabolism*,  pharmacology
Hydroxides / chemistry
Molecular Conformation
Receptors, G-Protein-Coupled / agonists,  chemistry,  metabolism*
Structure-Activity Relationship
Substrate Specificity
Reg. No./Substance:
0/Cholestanols; 0/GPBAR1 protein, human; 0/Hydroxides; 0/Ligands; 0/Receptors, G-Protein-Coupled; 14280-30-9/hydroxide ion

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Intimate Partner Aggression Perpetrated and Sustained by Male Afghanistan, Iraq, and Vietnam Veteran...
Next Document:  FAT/CD36 is localized in sarcolemma and in vesicle-like structures in subsarcolemma regions but not ...