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Journal of Southern Medical University ; (12): 72-76, 2015.
Artigo em Chinês | WPRIM | ID: wpr-239244

RESUMO

<p><b>OBJECTIVE</b>To investigate the inhibitory effects of tetramethoxystilbene, a selective CYP1B1 inhibitor, on adipogenic differentiation of C3H10T1/2 multi-potent mesenchymal cells.</p><p><b>METHODS</b>In vitro cultured C3H10T1/2 cells at full confluence were induced by adipogenic agents (10 µg/ml insulin, 2 µmol/L dexamethasone and 0.5 mmol/L 3-isobutyl-1-methylxanthine) and exposed simultaneously to TMS at the final concentrations of 1.0, 2.0 or 4.0 µg/ml. Oil Red-O staining was used to observe the cell differentiation. The expression of peroxisome proliferator-activated receptor gamma (PPARγ) and its target genes cluster of differentiation 36 (CD36) and fatty acid binding protein 4 (FABP4) were quantified by real-time RT-PCR and Western blotting.</p><p><b>RESULTS</b>Oil Red-O staining and TG contents revealed that TMS suppressed induced differentiation of C3H10T1/2 cells. TMS exposure of the cells dose-dependently decreased both mRNA and protein expressions of PPARγ, a key nuclear transcription factor during adipogenesis, and also lowered the mRNA expressions of PPARγ target genes CD36 and FABP4.</p><p><b>CONCLUSION</b>TMS can suppress adipogenic differentiation of C3H10T1/2 cells by inhibiting PPARγ</p>


Assuntos
Animais , Adipogenia , Diferenciação Celular , Células Cultivadas , Citocromo P-450 CYP1B1 , Inibidores das Enzimas do Citocromo P-450 , Farmacologia , Células-Tronco Mesenquimais , Biologia Celular , Camundongos Endogâmicos C3H , PPAR gama , Metabolismo , Células-Tronco Pluripotentes , Biologia Celular , RNA Mensageiro , Estilbenos , Farmacologia
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