Laboraotry Animal Center, Korea Research Institute of Bioscience and Biotechnology, University of Science and Technology, 125 Gwahak-ro, Yuseong-gu, Daejeon 305-806, Republic of Korea.
Food Chem. 2013 Nov 15;141(2):723-30. doi: 10.1016/j.foodchem.2013.04.036. Epub 2013 Apr 19.
This study was performed to investigate the effect of scoparone on the differentiation of 3T3-L1 preadipocytes. Scoparone inhibited triglyceride (TG) accumulation in the mature adipocytes, evidenced by Oil-red O staining and intracellular quantification. Real time-PCR analysis showed that scoparone significantly down-regulated the mRNA expression of key adipogenic transcription factors, PPARγ, C/EBPα, compared with mature adipocytes. Scoparone appeared to reduce mRNA expression of SREBP1c and FAS being related to the late stage of adipogenesis. Furthermore, aP2 and CD36/FAT, as adipocyte-specific genes, were decreased in mature adipocytes by scoparone treatment. Moreover, scoparone inhibited the up-regulated expression of PPARγ target genes by rosiglitazone to near that observed in cells treated with GW9662. The luciferase assay revealed that scoparone negatively regulates the transcriptional activity of PPARγ. Chromatin immunoprecipitation assay also showed that participation of scoparone in the regulation of PPARγ. Collectively, scoparone has a PPARγ antagonic effect and suppresses differentiation through down-regulation of adipogenic genes by PPARγ inhibition in 3T3-L1 preadipocytes.
本研究旨在探讨贯叶连翘素对 3T3-L1 前脂肪细胞分化的影响。油红 O 染色和细胞内定量分析表明,贯叶连翘素抑制成熟脂肪细胞中三酰甘油(TG)的积累。实时 PCR 分析显示,与成熟脂肪细胞相比,贯叶连翘素显著下调关键脂肪生成转录因子 PPARγ、C/EBPα 的 mRNA 表达。贯叶连翘素似乎降低了与脂肪生成晚期相关的 SREBP1c 和 FAS 的 mRNA 表达。此外,脂肪细胞特异性基因 aP2 和 CD36/FAT 在贯叶连翘素处理的成熟脂肪细胞中减少。此外,贯叶连翘素抑制了罗格列酮上调的 PPARγ 靶基因的表达,使其接近用 GW9662 处理的细胞中观察到的表达水平。荧光素酶测定显示贯叶连翘素负调控 PPARγ 的转录活性。染色质免疫沉淀分析也表明贯叶连翘素参与了 PPARγ 的调节。综上所述,贯叶连翘素具有 PPARγ 拮抗作用,并通过抑制 PPARγ 抑制脂肪生成基因的表达来抑制 3T3-L1 前脂肪细胞的分化。