Effects of a fatty acid synthase inhibitor on adipocyte differentiation of mouse 3T3-L1 cells
Abstract
AIM:
To investigate the influence of C75, a fatty acid synthase inhibitor, on adipocyte differentiation.
METHODS:
Mouse 3T3-L1 preadipocytes were induced to differentiation by insulin, isobutylmethylxanthine, and dexamethasone. Oil red O staining was performed and activity of glycerol-3-phosphate dehydrogenase (GPDH) was measured. The level of peroxisome proliferators-activated receptor gamma (PPARgamma) mRNA was assayed by semi-quantitative reverse transcription PCR.
RESULTS:
C75 blocked the adipogenic conversion in a dose-dependent manner and the inhibitory effects occurred both in the early phases (48 h) and in the latter phases (8 d) of the process. Treatment with C75 for 8 d induced more decrease in lipid content than 48 h (P<0.01). Treatment with C75 50 mg/L for 48 h or 8 d decreased GPDH activity by 52.8 % and 31.2 % of Vehicle, respectively. Treatment with C75 10-50 mg/L for 48 h or 8 d down-regulated PPARgamma mRNA expression compared with control (P<0.01).
CONCLUSION:
C75 blocked the adipocyte differentiation, which was related with down-regulation of PPARgamma mRNA.
Keywords:
To investigate the influence of C75, a fatty acid synthase inhibitor, on adipocyte differentiation.
METHODS:
Mouse 3T3-L1 preadipocytes were induced to differentiation by insulin, isobutylmethylxanthine, and dexamethasone. Oil red O staining was performed and activity of glycerol-3-phosphate dehydrogenase (GPDH) was measured. The level of peroxisome proliferators-activated receptor gamma (PPARgamma) mRNA was assayed by semi-quantitative reverse transcription PCR.
RESULTS:
C75 blocked the adipogenic conversion in a dose-dependent manner and the inhibitory effects occurred both in the early phases (48 h) and in the latter phases (8 d) of the process. Treatment with C75 for 8 d induced more decrease in lipid content than 48 h (P<0.01). Treatment with C75 50 mg/L for 48 h or 8 d decreased GPDH activity by 52.8 % and 31.2 % of Vehicle, respectively. Treatment with C75 10-50 mg/L for 48 h or 8 d down-regulated PPARgamma mRNA expression compared with control (P<0.01).
CONCLUSION:
C75 blocked the adipocyte differentiation, which was related with down-regulation of PPARgamma mRNA.