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Butein is a novel anti-adipogenic compound

机译:Butein是一种新型的抗脂肪形成化合物

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摘要

Rhus verniciflua Stokes (RVS) has been used as a traditional herbal medicine for its various biological activities including anti-adipogenic effects. Activity-guided separation led to the identification of the anti-adipogenic functions of butein. Butein, a novel anti-adipogenic compound, robustly suppressed lipid accumulation and inhibited expression of adipogenic markers. Molecular studies showed that activated transforming growth factor-β (TGF-β) and suppressed signal transducer and activator of transcription 3 (STAT3) signaling pathways were mediated by butein. Analysis of the temporal expression profiles suggests that TGF-β signaling precedes the STAT3 in the butein-mediated anti-adipogenic cascade. Small interfering RNA-mediated silencing of STAT3 or SMAD2/3 blunted the inhibitory effects of butein on adipogenesis indicating that an interaction between two signaling pathways is required for the action of butein. Upon butein treatments, stimulation of TGF-β signaling was still preserved in STAT3 silenced cells, whereas regulation of STAT3 signaling by butein was significantly impaired in SMAD2/3 silenced cells, further showing that TGF-β acts upstream of STAT3 in the butein-mediated anti-adipogenesis. Taken together, the present study shows that butein, a novel anti-adipogenic compound from RVS, inhibits adipocyte differentiation through the TGF-β pathway followed by STAT3 and peroxisome proliferator-activated receptor γ signaling, further implicating potential roles of butein in TGF-β- and STAT3-dysregulated diseases.
机译:红景天斯托克斯(RVS)已被用作传统草药,因为它具有多种生物活性,包括抗脂肪形成作用。活性指导的分离导致丁酸抗脂肪形成功能的鉴定。 Butein是一种新型的抗脂肪形成化合物,可强烈抑制脂质堆积并抑制脂肪形成标记的表达。分子研究表明,butein介导了活化的转化生长因子-β(TGF-β)和抑制的信号转导和转录激活因子3(STAT3)信号通路。对时间表达谱的分析表明,在酪蛋白介导的抗脂肪形成级联反应中,TGF-β信号传导先于STAT3。 STAT3或SMAD2 / 3的小干扰RNA介导的沉默减弱了丁酸酯对脂肪形成的抑制作用,表明丁酸酯的作用需要两个信号传导途径之间的相互作用。在丁烯酸治疗后,STAT3沉默的细胞中仍保留了TGF-β信号的刺激,而SMAD2 / 3沉默的细胞中丁烯酸对STAT3信号的调节明显受损,进一步表明TGF-β在丁烯酸介导的STAT3上游起作用抗脂肪生成。综上所述,本研究表明,丁香是一种来自RVS的新型抗脂肪形成化合物,其通过TGF-β途径,随后是STAT3和过氧化物酶体增殖物激活的受体γ信号传导来抑制脂肪细胞的分化,进一步暗示了丁烯在TGF-β中的潜在作用。 -和STAT3失调的疾病。

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