首页> 外文期刊>Lipids >cis-9,trans-11,cis-15 and cis-9,trans-13,cis-15 CLNA mixture activates PPARalpha in HEK293 and reduces triacylglycerols in 3T3-L1 cells.
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cis-9,trans-11,cis-15 and cis-9,trans-13,cis-15 CLNA mixture activates PPARalpha in HEK293 and reduces triacylglycerols in 3T3-L1 cells.

机译:顺式9,反式11,顺式15和顺式9,反式13,顺式15 CLNA混合物可激活HEK293中的PPARalpha,并减少3T3-L1细胞中的三酰基甘油。

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摘要

Scientific research is constantly working to find new molecules that are effective in preventing excessive accumulation of body fat. The aim of the present work was to assess the potential agonism on PPARalpha and PPARgamma of a conjugated linolenic acid (CLNA) isomer mixture, consisting of two CLNA isomers (cis-9,trans-11,cis-15 and cis-9,trans-13,cis-15). Secondly, we aimed to analyze the effects of this mixture on triacylglycerol accumulation in 3T3-L1 mature adipocytes. Luciferase transactivation assay was used to analyze whether the CLNA mixture activated PPARs. The expression of several enzymes and transcriptional factors involved in the main metabolic pathways that control triacylglycerol accumulation in adipocytes was assessed by real time RT-PCR in 3T3-L1 adipocytes treated for 20 h with the CLNA mixture. The mixture activated PPRE in cells with PPARalpha receptor over-expression, but not those with PPARgamma over-expression. Decreased triacylglycerol was found in treated adipocytes. The lowest dose (10 muM) increased HSL expression and the highest dose (100 muM) increased ATGL gene expression. The other genes analyzed remained unchanged. The hypothesis of an anti-obesity action of the analyzed CLNA mixture, based on increased lipid mobilization in adipose tissue, can be proposed.
机译:科学研究一直在努力寻找可以有效防止体内脂肪过度积聚的新分子。本工作的目的是评估由两种CLNA异构体(顺式9,反式11,顺式15和顺式9,反式)组成的共轭亚麻酸(CLNA)异构体混合物对PPARalpha和PPARgamma的潜在激动作用-13,cis-15)。其次,我们旨在分析该混合物对3T3-L1成熟脂肪细胞中三酰基甘油积累的影响。萤光素酶反式激活法用于分析CLNA混合物是否激活了PPAR。通过实时RT-PCR评估了用CLNA混合物处理20小时的3T3-L1脂肪细胞中,参与控制脂肪细胞中三酰甘油积累的主要代谢途径的几种酶和转录因子的表达。该混合物在具有PPARalpha受体过度表达的细胞中激活PPRE,但不会激活具有PPARgamma过度表达的细胞。在处理过的脂肪细胞中发现三酰甘油减少。最低剂量(10μM)增加HSL表达,最高剂量(100μM)增加ATGL基因表达。分析的其他基因保持不变。可以提出基于增加的脂肪组织中脂质动员的分析的CLNA混合物的抗肥胖作用的假说。

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