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槐米中选定的黄酮醇糖苷通过激活 3T3-L1 细胞中的 AMPK 促进葡萄糖摄取并抑制脂肪细胞分化。

The selected flavonol glycoside derived from Sophorae Flos improves glucose uptake and inhibits adipocyte differentiation via activation AMPK in 3T3-L1 cells.

机构信息

College of Pharmacy, Chungnam National University, Daejeon, South Korea.

出版信息

Bioorg Med Chem Lett. 2010 Oct 15;20(20):6076-81. doi: 10.1016/j.bmcl.2010.08.054. Epub 2010 Aug 16.

DOI:10.1016/j.bmcl.2010.08.054
PMID:20822902
Abstract

Among nine flavonols (1-9) obtained from Sophorae Flos, we first isolated compounds 4, 5, 8, and 9. These isolates (1-9) were evaluated for the phosphorylation of AMPK and ACC. Administered at 10 μM, 9 possessed high potent activity. Compound 9 displayed a dose-dependent stimulation of glucose uptake in 3T3-L1 cells, and this increase was obviously attenuated by compound C, an AMPK inhibitor. In addition, 9 also phosphorylated AMPK and its downstream substrate ACC in 3T3-L1 cells in a time- and dose-dependent manner. Moreover, we discovered that compound C inhibits 9-stimulated ACC phosphorylation and motivated the 9-inhibited C/EBPα and PPARγ, and FAS gene expression, significantly. These results revealed the role of the AMPK downstream signaling pathway in 9-improved glucose metabolism in 3T3-L1 cells and 9-inhibited adipocyte differentiation. Differentiation was investigated by Oil Red O staining activity after 9 administration (0-20 μM) in 6 days. Compound 9 decreased mean droplet size in a dose-dependent manner. The results revealed that 9 blocked adipogenic conversion in 3T3-L1 cells together with several significant downregulating adipocyte-specific transcription factors, including PPARγ, C/EBPα, and SREBP1. It also reduced FAS gene expression in a dose-dependent manner, which is crucial for adipogenesis in vitro.

摘要

从槐米中分离得到的 9 种黄酮醇(1-9)中,我们首次分离得到了化合物 4、5、8 和 9。这些分离物(1-9)被评估了对 AMPK 和 ACC 的磷酸化作用。在 10 μM 时,化合物 9 表现出对 AMPK 和 ACC 的高度有效活性。化合物 9 在 3T3-L1 细胞中显示出葡萄糖摄取的剂量依赖性刺激作用,而 AMPK 抑制剂化合物 C 明显减弱了这种增加。此外,化合物 9 还以时间和剂量依赖的方式在 3T3-L1 细胞中磷酸化 AMPK 及其下游底物 ACC。此外,我们发现化合物 C 抑制 9 刺激的 ACC 磷酸化,并显著促进了 9 抑制的 C/EBPα 和 PPARγ 以及 FAS 基因表达。这些结果揭示了 AMPK 下游信号通路在 9 改善 3T3-L1 细胞葡萄糖代谢和 9 抑制脂肪细胞分化中的作用。在 9 处理(0-20 μM)6 天后,通过油红 O 染色活性研究 9 对脂肪细胞分化的抑制作用。化合物 9 以剂量依赖的方式降低平均液滴大小。结果表明,9 阻断了 3T3-L1 细胞的脂肪生成转化,同时显著下调了几个脂肪细胞特异性转录因子,包括 PPARγ、C/EBPα 和 SREBP1。它还以剂量依赖的方式降低 FAS 基因表达,这对于体外脂肪生成至关重要。

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