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传统中药华西獐牙菜抑制脂肪细胞分化和脂肪生成。

Inhibition of adipocyte differentiation and adipogenesis by the traditional Chinese herb Sibiraea angustata.

机构信息

Biomedicine Research Institute and College of Life Sciences, Beijing Normal University, Beijing 100875, China.

出版信息

Exp Biol Med (Maywood). 2010 Dec;235(12):1442-9. doi: 10.1258/ebm.2010.010167. Epub 2010 Oct 20.

Abstract

Obesity has become a major health concern due to its strong association with the metabolic syndrome. Inhibition of adipocyte differentiation represents a key strategy to inhibit obesity. Sibiraea angustata (SA), a traditional Chinese herb, has a wide range of pharmacological effects, such as improving digestive functions. Here, we report a novel antiadipogenic effect of SA. By using the SA water extract (SAW), SA acetic ether extract (SAA) and the 3T3-L1 model of adipocyte differentiation and adipogenesis, we showed that both SAW and SAA impaired the proliferation and adipo-differentiation of 3T3-L1 in a dose- and time-dependent manner. At the molecular level, treatment of 3T3-L1 cells with SAW or SAA inhibited the expression of the key adipocyte differentiation regulator CCAAT enhancer binding protein β (C/EBPβ), as well as peroxisome proliferator activated receptor γ, adipocyte protein-2, lipoprotein lipase and glucose transporter 4. Cell cycle analysis showed that both SAW and SAA blocked cell cycle at the G1-S transition phase, causing cells to remain in the preadipocyte state. The expression of CyclinA and cyclin-dependent kinase 2 was also inhibited by SAW and SAA. Treatment with SAW also prevented the localization of C/EBPβ to the centromeres. Taken together, our results show that SA has a potent antiadipogenic effect in 3T3-L1 cells due to the inhibition of adipocyte differentiation and adipogenesis. We propose that SA may be used as a safe and effective neutraceutical to manage obesity.

摘要

肥胖症已成为一个主要的健康问题,因为它与代谢综合征密切相关。抑制脂肪细胞分化代表了抑制肥胖的一个关键策略。八角枫(SA)是一种传统的中药,具有广泛的药理作用,如改善消化功能。在这里,我们报告了 SA 的一种新的抗脂肪生成作用。通过使用 SA 水提取物(SAW)、SA 乙酸乙酯提取物(SAA)和 3T3-L1 脂肪细胞分化和脂肪生成模型,我们表明,SAW 和 SAA 均以剂量和时间依赖的方式损害 3T3-L1 的增殖和脂肪分化。在分子水平上,用 SAW 或 SAA 处理 3T3-L1 细胞抑制了关键脂肪细胞分化调节因子 CCAAT 增强子结合蛋白β(C/EBPβ)的表达,以及过氧化物酶体增殖物激活受体γ、脂肪细胞蛋白-2、脂蛋白脂肪酶和葡萄糖转运蛋白 4。细胞周期分析表明,SAW 和 SAA 均阻止细胞周期在 G1-S 过渡阶段,使细胞保持在前脂肪细胞状态。细胞周期蛋白 A 和细胞周期蛋白依赖性激酶 2 的表达也被 SAW 和 SAA 抑制。SAW 处理还阻止了 C/EBPβ向着丝粒的定位。总之,我们的结果表明,SA 通过抑制脂肪细胞分化和脂肪生成,对 3T3-L1 细胞具有强大的抗脂肪生成作用。我们提出,SA 可作为一种安全有效的营养保健品,用于治疗肥胖症。

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