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DHA 调节小鼠脂肪组织和肝脏中的脂肪生成和脂肪分解基因。

DHA regulates lipogenesis and lipolysis genes in mice adipose and liver.

机构信息

College of Animal Science and Technology, Northwest A&F University, 712100, Yangling, Shaanxi, China.

出版信息

Mol Biol Rep. 2011 Feb;38(2):731-7. doi: 10.1007/s11033-010-0160-9. Epub 2010 Apr 11.

Abstract

Docosahexaenoic acid (DHA) is one kind of ω-3 polyunsaturated fatty acids (PUFAs) and plays an important role in lipid metabolism. In this research, mice were daily intragastric administrated with DHA for 3 weeks. Subcutaneous adipose tissue and liver were separated every week, RNA was extracted. Peroxisome proliferator-activated receptor (PPARγ), Sterol regulatory element binding protein-1c (SREBP-1c), Fatty acid synthetase (FAS), Hormone sensitive lipase (HSL) and triglyceride hydrolase TGH genes expression were detected by quantitative PCR. Data showed that, DHA up-regulated PPARγ, HSL and TGH in adipose tissue, but it had no effect on SREBP-1c and FAS expression. However, in liver there were some differences in regulating these genes. PPARγ, SREBP-1c and FAS were down-regulated, HSL was up-regulated and TGH had no change. These results indicated that DHA played different regulating roles in lipid metabolism in different tissues. In adipose tissue, DHA increased the expression of lipogenesis and lipolysis genes. In liver lipogenesis genes were decreased, but lipolysis genes were increased by DHA. In conclusion, DHA could reduce body fat mass through regulating lipogenesis and lipolysis genes.

摘要

二十二碳六烯酸(DHA)是一种ω-3 多不饱和脂肪酸(PUFA),在脂质代谢中发挥重要作用。在这项研究中,小鼠每天经胃内给予 DHA 3 周。每周分离皮下脂肪组织和肝脏,提取 RNA。通过定量 PCR 检测过氧化物酶体增殖物激活受体(PPARγ)、固醇调节元件结合蛋白-1c(SREBP-1c)、脂肪酸合成酶(FAS)、激素敏感脂肪酶(HSL)和甘油三酯水解酶 TGH 基因的表达。结果表明,DHA 在上皮组织中上调了 PPARγ、HSL 和 TGH,但对 SREBP-1c 和 FAS 的表达没有影响。然而,在肝脏中,这些基因的调节存在一些差异。PPARγ、SREBP-1c 和 FAS 下调,HSL 上调,TGH 没有变化。这些结果表明,DHA 在不同组织中对脂质代谢发挥不同的调节作用。在上皮组织中,DHA 增加了脂肪生成和脂肪分解基因的表达。在肝脏中,DHA 下调了脂肪生成基因,但上调了脂肪分解基因。总之,DHA 通过调节脂肪生成和脂肪分解基因来减少体脂肪量。

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