Department of Bioscience and Biotechnology, BK21 Graduate Program, Sejong University, Seoul, Korea.
J Agric Food Chem. 2012 Apr 18;60(15):3853-60. doi: 10.1021/jf204514a. Epub 2012 Apr 6.
This study investigated the antiadipogenic activity of black pepper extract and its constituent piperine in 3T3-L1 preadipocytes as well as the underlying molecular mechanisms. Both black pepper extract and piperine, without affecting cytotoxicity, strongly inhibited the adipocyte differentiation of 3T3-L1 cells. The mRNA expression of the master adipogenic transcription factors, PPARγ, SREBP-1c, and C/EBPβ, was markedly decreased. Intriguingly, mRNA levels of PPARγ target genes were also down-regulated. Moreover, a luciferase reporter assay indicated that pipierine significantly represses the rosiglitazone-induced PPARγ transcriptional activity. Finally, GST-pull down assays demonstrated that piperine disrupts the rosiglitazone-dependent interaction between PPARγ and coactivator CBP. Genome-wide analysis using microarray further supports the role of piperine in regulating genes associated with lipid metabolism. Overall, these results suggest that piperine, a major component of black pepper, attenuates fat cell differentiation by down-regulating PPARγ activity as well as suppressing PPARγ expression, thus leading to potential treatment for obesity-related diseases.
本研究探讨了黑胡椒提取物及其成分胡椒碱在 3T3-L1 前脂肪细胞中的抗脂肪生成活性及其潜在的分子机制。黑胡椒提取物和胡椒碱均不影响细胞毒性,强烈抑制 3T3-L1 细胞的脂肪细胞分化。主脂肪生成转录因子 PPARγ、SREBP-1c 和 C/EBPβ 的 mRNA 表达明显下调。有趣的是,PPARγ 靶基因的 mRNA 水平也下调。此外,荧光素酶报告基因测定表明胡椒碱显著抑制罗格列酮诱导的 PPARγ 转录活性。最后,GST-pull down 测定表明胡椒碱破坏了罗格列酮依赖的 PPARγ 和共激活因子 CBP 之间的相互作用。使用微阵列进行的全基因组分析进一步支持胡椒碱在调节与脂质代谢相关的基因中的作用。总的来说,这些结果表明,胡椒碱作为黑胡椒的主要成分,通过下调 PPARγ 活性和抑制 PPARγ 表达来减弱脂肪细胞分化,从而为肥胖相关疾病的治疗提供了潜在的可能。