Lee S H, Kim K-Y, Ryu S Y, Yoon Y, Hahm D-H, Kang S A, Cho S H, Lim J-S, Moon E-Y, Yoon S R, Lee H G, Yoon D Y, Yang Y
Department of Biological Science, Sookmyung Women's University, Seoul 140-742, Korea.
Cell Mol Biol (Noisy-le-grand). 2010 Jan 24;56 Suppl:OL1215-22.
Asarone is a molecule found in certain plants such as Acorus calamus, the root of which is used in traditional medicine to treat diabetes. We determined the molecular mechanism underlying the anti-diabetic activity of asarone. Treatment of asarone significantly inhibited the differentiation of 3T3-L1 preadipocytes through suppression of expression of the transcription factors, CCAAT/enhancer binding protein-alpha and peroxisome proliferator activated receptor-gamma, which activate adipogenesis. Intracellular triglyceride levels were reduced by asarone in a dose-dependent manner and asarone treatment stimulated the phosphorylation of hormone-sensitive lipase. Together, the present findings indicate that asarone inhibits adipogenesis by down-regulation of PPARgamma and C/EBPalpha and reduces lipid accumulation by stimulation of lipolysis through an increase in hormone-sensitive lipase activity.
细辛脑是一种存在于某些植物中的分子,如菖蒲,其根在传统医学中用于治疗糖尿病。我们确定了细辛脑抗糖尿病活性的分子机制。细辛脑处理通过抑制转录因子CCAAT/增强子结合蛋白α和过氧化物酶体增殖物激活受体γ的表达,显著抑制3T3-L1前脂肪细胞的分化,这两种转录因子可激活脂肪生成。细辛脑以剂量依赖的方式降低细胞内甘油三酯水平,并且细辛脑处理刺激了激素敏感性脂肪酶磷酸化。总之,目前的研究结果表明,细辛脑通过下调PPARγ和C/EBPα来抑制脂肪生成,并通过增加激素敏感性脂肪酶活性刺激脂肪分解来减少脂质积累。