Han Younho, Lee Sung Ho, Lee Ik-Soo, Lee Kwang Youl
College of Pharmacy & Research Institute of Drug Development, Chonnam National University, Gwangju, Republic of Korea.
College of Pharmacy & Research Institute of Drug Development, Chonnam National University, Gwangju, Republic of Korea.
Food Chem Toxicol. 2017 Aug;106(Pt A):17-24. doi: 10.1016/j.fct.2017.05.032. Epub 2017 May 18.
Chalcones, the biosynthetic precursors of flavonoids and isoflavonoids abundant in edible plants, possess a number of pharmacological properties, and there is growing evidence that chalcone derivatives inhibit TNF-α mediated insulin resistance. The aim of the present study was to define the effects of 4-methoxychalcone (4-MC) on adipocyte differentiation and to determine the underlying molecular mechanism. We investigated the effects of 4-MC on adipocyte differentiation and lipid accumulation, and expression of adipogenic genes in 3T3-L1 cells. Additionally, treatment with 4-MC significantly increased the PPARγ-induced transcriptional activity and 4-MC also enhanced the DNA binding affinity of PPARγ to the proliferator-activated receptor response elements (PPRE) at target promoters. Next, we tested the effect of 4-MC on the inhibition induced by TNF-α on adipocyte differentiation. Treatment with 4-MC enhanced the lipid accumulation and strongly up-regulated the expression of adipogenic markers, including PPARγ, aP2, FAS, and adiponectin during adipocyte differentiation. Finally, 4-MC attenuated the inhibitory effect of TNF-α on adipocyte differentiation and adiponectin expression and subsequently regulated the expression and secretion of various adipokines that are involved in insulin sensitivity. This study clearly demonstrates that 4-MC enhanced adipocyte differentiation, in part, by its potent effects on PPARγ activation and by its reverse effect on TNF-α.
查耳酮是可食用植物中大量存在的黄酮类化合物和异黄酮类化合物的生物合成前体,具有多种药理特性,并且越来越多的证据表明查耳酮衍生物可抑制肿瘤坏死因子-α(TNF-α)介导的胰岛素抵抗。本研究的目的是确定4-甲氧基查耳酮(4-MC)对脂肪细胞分化的影响,并确定其潜在的分子机制。我们研究了4-MC对3T3-L1细胞中脂肪细胞分化、脂质积累和成脂基因表达的影响。此外,4-MC处理显著增加了过氧化物酶体增殖物激活受体γ(PPARγ)诱导的转录活性,并且4-MC还增强了PPARγ与靶启动子上的增殖物激活受体反应元件(PPRE)的DNA结合亲和力。接下来,我们测试了4-MC对TNF-α诱导的脂肪细胞分化抑制作用的影响。在脂肪细胞分化过程中,4-MC处理增强了脂质积累,并强烈上调了包括PPARγ、脂肪细胞脂肪酸结合蛋白(aP2)、脂肪酸合酶(FAS)和脂联素在内的成脂标志物的表达。最后,4-MC减弱了TNF-α对脂肪细胞分化和脂联素表达的抑制作用,随后调节了参与胰岛素敏感性的各种脂肪因子的表达和分泌。本研究清楚地表明,4-MC部分通过其对PPARγ激活的强大作用以及对TNF-α的反向作用增强了脂肪细胞分化。