首页> 外文期刊>Marine biotechnology >1-(3',5'-dihydroxyphenoxy)-7-(2aEuro(3),4aEuro(3),6-trihydroxyphenoxy)-2,4,9-trihydroxydibenzo-1,4-dioxin Inhibits Adipocyte Differentiation of 3T3-L1 Fibroblasts
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1-(3',5'-dihydroxyphenoxy)-7-(2aEuro(3),4aEuro(3),6-trihydroxyphenoxy)-2,4,9-trihydroxydibenzo-1,4-dioxin Inhibits Adipocyte Differentiation of 3T3-L1 Fibroblasts

机译:1-(3',5'-dihydroxyphenoxy)-7-(2aEuro(3),4aEuro(3),6-trihydroxyphenoxy)-2,4,9-trihydroxydibenzo-1,4-dioxin抑制3T3-L1的脂肪细胞分化成纤维细胞

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In this study, we isolated the phloroglucinol derivative, 1-(3',5'-dihydroxyphenoxy)-7-(2aEuro(3),4aEuro(3),6-trihydroxyphenoxy)-2,4,9-trihydroxydibenzo-1,4-dioxin (1), from Ecklonia cava and evaluated its potential inhibition on adipocyte differentiation in 3T3-L1 cells. Lipid accumulation along with the expression of several genes associated with adipogenesis and lipolysis was examined at the end of differentiation. Lipid accumulation level was examined by measuring triglyceride content and Oil-Red O staining. The expression levels of several genes and proteins were examined using reverse-transcription polymerase chain reaction (RT-PCR), real-time RT-PCR, and Western blot analysis. Compound 1 significantly reduced lipid accumulation and downregulated peroxisome proliferator-activated receptor-gamma, sterol regulatory element-binding protein 1c, and CCAAT/enhancer-binding proteins alpha in a dose-dependent manner. Moreover, the presence of compound 1 induced downregulation of adipogenic target genes such as fatty acid binding protein 4, fatty acid transport protein 1, fatty acid synthase, acyl-CoA synthetase 1, lipoprotein lipase, and leptin. According to the lipolytic response, compound 1 downregulated perilipin and hormone-sensitive lipase while upregulating tumor necrosis factor alpha. Therefore, these results suggest that compound 1 might decrease lipid accumulation during adipocyte differentiation by modulating adipogenesis and lipogenesis. Furthermore, compound 1 could be developed as a functional agent effective in improving obesity.
机译:在这项研究中,我们分离了间苯三酚衍生物1-(3',5'-dihydroxyphenoxy)-7-(2aEuro(3),4aEuro(3),6-trihydroxyphenoxy)-2,4,9-trihydroxydibenzo-1,来自Ecklonia cava的4-dioxin(1),评估了其对3T3-L1细胞中脂肪细胞分化的潜在抑制作用。在分化结束时检查脂质积累以及与脂肪形成和脂解相关的几种基因的表达。通过测量甘油三酸酯含量和油红O染色检查脂质积累水平。使用逆转录聚合酶链反应(RT-PCR),实时RT-PCR和Western blot分析检查了几种基因和蛋白质的表达水平。化合物1以剂量依赖的方式显着减少脂质积聚并下调过氧化物酶体增殖物激活的受体-γ,固醇调节元件结合蛋白1c和CCAAT /增强剂结合蛋白α。此外,化合物1的存在诱导脂肪形成靶基因例如脂肪酸结合蛋白4,脂肪酸转运蛋白1,脂肪酸合酶,酰基辅酶A合成酶1,脂蛋白脂肪酶和瘦蛋白的下调。根据脂解反应,化合物1下调周脂素和激素敏感性脂肪酶,同时上调肿瘤坏死因子α。因此,这些结果表明化合物1可能通过调节脂肪生成和脂肪生成而减少脂肪细胞分化过程中的脂质积累。此外,可以将化合物1开发为有效改善肥胖症的功能剂。

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