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Fucoidan from Marine Brown Algae Inhibits Lipid Accumulation

机译:海洋褐藻中的褐藻糖胶抑制脂质积累

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摘要

In this study, we elucidated the inhibitory effect of fucoidan from marine brown algae on the lipid accumulation in differentiated 3T3-L1 adipocytes and its mechanism. The treatment of fucoidan in a dose-dependent manner was examined on lipid inhibition in 3T3-L1 cells by using Oil Red O staining. Fucoidan showed high lipid inhibition activity at 200 μg/mL concentration (P < 0.001). Lipolytic activity in adipocytes is highly dependent on hormone sensitive lipase (HSL), which is one of the most important targets of lipolytic regulation. Here, we examined the biological response of fucoidan on the protein level of lipolysis pathway. The expressed protein levels of total hormone sensitive lipase (HSL) and its activated form, phosphorylated-HSL were significantly increased at concentration of 200 μg/mL fucoidan. Furthermore, insulin-induced 2-deoxy-d-[3H] glucose uptake was decreased up to 51% in fucoidan-treated cells as compared to control. Since increase of HSL and p-HSL expression and decrease of glucose uptake into adipocytes are known to lead to stimulation of lipolysis, our results suggest that fucoidan reduces lipid accumulation by stimulating lipolysis. Therefore, these results suggest that fucoidan can be useful for the prevention or treatment of obesity due to its stimulatory lipolysis.
机译:在这项研究中,我们阐明了海藻褐藻糖胶对分化的3T3-L1脂肪细胞中脂质蓄积的抑制作用及其机理。使用油红O染色检查了岩藻依聚糖在3T3-L1细胞中对脂质抑制的剂量依赖性方式。岩藻依聚糖在200μg/ mL浓度下显示出高脂质抑制活性(P <0.001)。脂肪细胞中的脂解活性高度依赖于激素敏感性脂肪酶(HSL),后者是脂解调节的最重要目标之一。在这里,我们检查了岩藻依聚糖对脂解途径蛋白质水平的生物学反应。当浓度为200μg/ mL岩藻依聚糖时,总激素敏感性脂肪酶(HSL)及其活化形式磷酸化HSL的表达蛋白水平显着增加。此外,与对照相比,在岩藻依聚糖处理的细胞中,胰岛素诱导的2-脱氧-d-[ 3 H]葡萄糖摄取降低了高达51%。由于已知HSL和p-HSL表达的增加以及脂肪细胞摄取葡萄糖的减少会导致脂肪分解的刺激,因此我们的结果表明岩藻依聚糖通过刺激脂肪分解而减少了脂质蓄积。因此,这些结果表明岩藻依聚糖由于其刺激性脂解作用而可用于预防或治疗肥胖。

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