PT  - JOURNAL ARTICLE
AU  - Qi Sun
AU  - Akira Hirasawa
AU  - Takafumi Hara
AU  - Ikuo Kimura
AU  - Tetsuya Adachi
AU  - Takeo Awaji
AU  - Masaji Ishiguro
AU  - Takayoshi Suzuki
AU  - Naoki Miyata
AU  - Gozoh Tsujimoto
TI  - Structure-Activity Relationships of GPR120 Agonists Based on a Docking Simulation
AID  - 10.1124/mol.110.066324
DP  - 2010 Nov 01
TA  - Molecular Pharmacology
PG  - 804--810
VI  - 78
IP  - 5
4099  - http://molpharm.aspetjournals.org/content/78/5/804.short
4100  - http://molpharm.aspetjournals.org/content/78/5/804.full
SO  - Mol Pharmacol2010 Nov 01; 78
AB  - GPR120 is a G protein-coupled receptor expressed preferentially in the intestinal tract and adipose tissue, that has been implicated in mediating free fatty acid-stimulated glucagon-like peptide-1 (GLP-1) secretion. To develop GPR120-specific agonists, a series of compounds (denoted as NCG compounds) derived from a peroxisome proliferator-activated receptor γ agonist were synthesized, and their structure-activity relationships as GPR120 agonists were explored. To examine the agonistic activities of these newly synthesized NCG compounds, and of compounds already shown to have GPR120 agonistic activity (grifolic acid and MEDICA16), we conducted docking simulation in a GPR120 homology model that was developed on the basis of a photoactivated model derived from the crystal structure of bovine rhodopsin. We calculated the hydrogen bonding energies between the compounds and the GPR120 model. These energies correlated well with the GPR120 agonistic activity of the compounds (R2 = 0.73). NCG21, the NCG compound with the lowest calculated hydrogen bonding energy, showed the most potent extracellular signal-regulated kinase (ERK) activation in a cloned GPR120 system. Furthermore, NCG21 potently activated ERK, intracellular calcium responses and GLP-1 secretion in murine enteroendocrine STC-1 cells that express GPR120 endogenously. Moreover, administration of NCG21 into the mouse colon caused an increase in plasma GLP-1 levels. Taken together, our present study showed that a docking simulation using a GPR120 homology model might be useful to predict the agonistic activity of compounds.