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Baicalein inhibits lipid accumulation by regulating early adipogenesis and m-TOR signaling

机译:黄ical素通过调节早期脂肪生成和m-TOR信号传导抑制脂质蓄积

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摘要

Baicalein is a type of flavonoid that originates from Scutellaria baicalensis. In this study, we examined how baicalein inhibits lipid accumulation during adipogenesis in 3T3-L1 cells. Our data show that baicalein inhibited lipid accumulation during adipogenesis in a dose-dependent manner. Baicalein inhibition was limited to the early adipogenic stage. Cell cycle analysis showed that baicalein induced cell cycle arrest in the G0/G1 phase through cyclin downregulation. In addition, baicalein suppressed the mRNA expression of early adipogenic factors leading to downregulation of late adipogenic factors at mRNA and protein levels. Inhibition of adipogenic factors by baicalein was correlated with downregulation of lipid synthetic enzymes. Additionally, baicalein negatively regulated the m-TOR signaling pathway involved in lipid accumulation during adipogenesis, thus inhibiting phosphorylation of m-TOR and p70S6 K. In a zebraflsh study, baicalein significantly reduced lipid accumulation in Nile Red staining. Consistent with a report using cell lines, mRNA expression of adipogenic factors was decreased in a dose-dependent manner by baicalein. This result reflects a reduction in total triglyceride levels based on a triglyceride assay. Our data suggest that baicalein inhibits lipid accumulation by controlling the cell cycle and m-TOR signaling in 3T3-L1 cells, and its anti-adipogenic effect was found in a zebrafish model.
机译:黄ical素是源自黄ba的一种类黄酮。在这项研究中,我们检查了黄ical素如何抑制3T3-L1细胞在脂肪形成过程中的脂质蓄积。我们的数据表明黄ba素以剂量依赖的方式抑制脂肪生成过程中的脂质蓄积。黄ical素的抑制作用仅限于成脂早期。细胞周期分析表明,黄ical苷通过细胞周期蛋白下调诱导了G0 / G1期细胞周期停滞。此外,黄ical素抑制早期成脂因子的mRNA表达,从而导致晚期成脂因子在mRNA和蛋白质水平上的下调。黄ical素对脂肪形成因子的抑制作用与脂质合成酶的下调有关。此外,黄ical苷负调控脂肪形成过程中参与脂质蓄积的m-TOR信号通路,从而抑制m-TOR和p70S6 K的磷酸化。在zebraflsh研究中,黄ical苷显着减少了尼罗河红染色中的脂质蓄积。与使用细胞系的报道一致,黄ical苷以剂量依赖性方式降低成脂因子的mRNA表达。该结果反映了基于甘油三酸酯测定法的总甘油三酸酯水平的降低。我们的数据表明,黄e素通过控制3T3-L1细胞的细胞周期和m-TOR信号传导来抑制脂质蓄积,并且在斑马鱼模型中发现了其抗脂肪形成作用。

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