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Anti-Obesity Effect of Standardized Extract of Microalga Phaeodactylum tricornutum Containing Fucoxanthin

机译:含褐藻黄质的微藻微角藻标准提取物的抗肥胖作用

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摘要

Fucoxanthin (FX), a marine carotenoid found in macroalgae and microalgae, exhibits several beneficial effects to health. The anti-obesity activity of FX is well documented, but FX has not been mass-produced or applied extensively or commercially because of limited availability of raw materials and complex extraction techniques. In this study, we investigated the anti-obesity effect of standardized FX powder (Phaeodactylum extract (PE)) developed from microalga Phaeodactylum tricornutum as a commercial functional food. The effects of PE on adipogenesis inhibition in 3T3-L1 adipocytes and anti-obesity in high-fat diet (HFD)-fed C57BL/6J mice were evaluated. PE and FX dose-dependently decreased intracellular lipid contents in adipocytes without cytotoxicity. In HFD-fed obese mice, PE supplementation for six weeks decreased body weight, organ weight, and adipocyte size. In the serum parameter analysis, the PE-treated groups showed attenuation of lipid metabolism dysfunction and liver damage induced by HFD. In the liver, uncoupling protein-1 (UCP1) upregulation and peroxisome proliferator activated receptor γ (PPARγ) downregulation were detected in the PE-treated groups. Additionally, micro computed tomography revealed lower fat accumulation in PE-treated groups compared to that in the HFD group. These results indicate that PE exerts anti-obesity effects by inhibiting adipocytic lipogenesis, inducing fat mass reduction and decreasing intracellular lipid content, adipocyte size, and adipose weight.
机译:Fucoxanthin(FX)是在大型藻类和微藻类中发现的一种海洋类胡萝卜素,对健康具有多种有益作用。 FX的抗肥胖活性已得到充分证明,但由于原材料的可获得性和复杂的提取技术的限制,FX尚未大规模生产或广泛应用或商业应用。在这项研究中,我们调查了从微藻三角藻(Triaeutumumcorncornutum)开发的作为商业功能食品的标准化FX粉末(岩藻提取物(PE))的抗肥胖作用。评估了PE对高脂饮食(HFD)喂养的C57BL / 6J小鼠中3T3-L1脂肪细胞中脂肪形成的抑制作用和抗肥胖作用。 PE和FX剂量依赖性地降低了脂肪细胞中的细胞内脂质含量,而没有细胞毒性。在由HFD喂养的肥胖小鼠中,补充PE六周可减少体重,器官重量和脂肪细胞大小。在血清参数分析中,PE处理组显示了HFD诱导的脂质代谢功能障碍和肝损害的减轻。在肝脏中,在PE治疗组中检测到解偶联蛋白1(UCP1)上调和过氧化物酶体增殖物激活的受体γ(PPARγ)下调。此外,与HFD组相比,微型计算机断层扫描显示,PE治疗组的脂肪堆积较低。这些结果表明,PE通过抑制脂肪细胞的脂肪生成,诱导脂肪减少和降低细胞内脂质含量,脂肪细胞大小和脂肪重量而发挥抗肥胖作用。

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