Establishment and application of screening methods for non-agonist PPARγ ligand.
- Author:
Yi HUAN
;
Jun PENG
;
Yue WANG
;
Chun-Ming JIA
;
Ke WANG
;
Ke-Hua WANG
;
Zhi-Qiang FENG
;
Zhu-Fang SHEN
- Publication Type:Journal Article
- MeSH:
Genes, Reporter;
Hepatocytes;
Hypoglycemic Agents;
chemistry;
Ligands;
PPAR gamma;
agonists;
chemistry;
Plasmids;
Response Elements;
Sulfonamides;
chemistry;
Transcriptional Activation
- From:
Acta Pharmaceutica Sinica
2014;49(12):1658-1664
- CountryChina
- Language:Chinese
-
Abstract:
In-vitro assay methods were established to evaluate transactivation and binding activity of compounds on peroxisome proliferator-activated receptor y (PPARγ). Firstly, plasmids were constructed for transactivation assay of PPARγ response element (PPRE) triggered reporter gene expression, and for cell-based binding activity assay of the chimeric receptor, which was fused with PPARγ ligand binding domain (LBD) and yeast transcriptional activator Gal4. Secondly, by using PPARy competitive binding assay based on time resolved-fluorescence resonance energy transfer (TR-FRET), affinities of compounds and drugs to PPARγ were evaluated. In application of these above methods, the PPARγ activating potency and characteristics of different compounds were evaluated, and a novel benzeneselfonamide derivative, ZLJ01, was found to have comparable binding activity and affinity with the well-known PPARy agonist, but lack of PPRE mediated transactivation activity. In preliminary study on in-vitro hypoglycemic activity, ZLJ1 was found to promote insulin-stimulated glucose uptake by liver cells. Therefore, we believe that combining transactivation and binding activity as well as affinity evaluation, the system could be used to screen non-agonist PPARγ ligand as anovel PPARγ modulator
