脂肪生成
脂肪细胞
过剩4
3T3-L1
过氧化物酶体增殖物激活受体
脂蛋白脂酶
内分泌学
脂肪组织
内科学
生物
曲格列酮
脂肪细胞蛋白2
白色脂肪组织
葡萄糖转运蛋白
化学
信使核糖核酸
基因表达
细胞生物学
转录因子
Ccaat增强子结合蛋白
下调和上调
过氧化物酶体增殖物激活受体γ
生物化学
细胞分化
核受体
分子生物学
基因表达调控
转录调控
增强子
油红O
受体
胰岛素
脂肪酸
医学
作者
Mi‐Jin Yim,Masashi Hosokawa,Yoshiyuki Mizushina,Hiromi Yoshida,Yasunori Saito,Kazuo Miyashita
摘要
Fucoxanthin is converted to fucoxanthinol and amarouciaxanthin A in mice. It was previously reported that fucoxanthinol attenuated the adipogenesis of 3T3-L1 cells. However, the effects of amarouciaxanthin A on adipocyte differentiation have not been clarified. This study examined the effects of amarouciaxanthin A on 3T3-L1 adipogenesis by comparing the effects of fucoxanthinol, isofucoxanthinol, and amarouciaxanthin B. Amarouciaxanthin A significantly decreased glycerol-3-phosphate dehydrogenase (GPDH) activity, which was measured as an indicator of adipocyte differentiation. The suppressive effect of amarouciaxanthin A was stronger than that of fucoxanthinol, amarouciaxanthin B, and isofucoxanthinol. The mRNA expressions of adipocyte fatty acid-binding protein (aP2), lipoprotein lipase (LPL), and glucose-transporter 4 (Glut4) in 3T3-L1 cells were markedly down-regulated by amarouciaxanthin A compared to fucoxanthinol. Furthermore, the expression levels of peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT-enhancer-binding protein α (C/EBPα),, which are the key adipogenic transcriptional factors, were also decreased by amarouciaxanthin A during adipocyte differentiation. These results show that amarouciaxanthin A, which is a dominant metabolite of fucoxanthin in white adipose tissue, suppressed 3T3-L1 adipocyte differentiation.
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