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首页> 外文期刊>The Journal of Nutritional Biochemistry >Down-regulation in muscle and liver lipogenic genes: EPA ethyl ester treatment in lean and overweight (high-fat-fed) rats
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Down-regulation in muscle and liver lipogenic genes: EPA ethyl ester treatment in lean and overweight (high-fat-fed) rats

机译:肌肉和肝脏脂肪形成基因的下调:瘦和超重(高脂饮食)大鼠的EPA乙酯治疗

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摘要

The precise mechanisms by which s-3 fatty acids improve fat metabolism are not completely understood. This study was designed to determine the effects of eicosapentaenoic acid (EPA) ethyl ester administration on the expression levels of several muscle, liver and adipose tissue genes involved in lipogenesis and fatty acid oxidation pathways. Male Wistar rats fed a standard diet (control animals) or a high-fat diet were treated daily by oral gavage with EPA ethyl ester (1g/kg) for 5 weeks. The high-fat diet caused a very significant increase in plasma cholesterol (P<.01) levels, which was reverted by EPA (P<.001). A significant decrease in circulating triglyceride levels (P<.05) was also observed in EPA-treated groups. EPA administration induced a significant down-regulation in some lipogenic genes such as muscle acetyl CoA carboxylase o (ACC o) (P<.05) and liver fatty acid synthase (FAS) (P<.05). Furthermore, a decrease in glucokinase (GK) gene expression was observed in EPA-treated animals fed a control diet (P<.01), whereas a significant increase in GK mRNA levels was found in groups fed a high-fat diet. On the other hand, no alterations in genes involved in o-oxidation, such acetyl CoA synthase 4 (ACS4), acetyl CoA synthase 5 (ACS5) or acetyl CoA oxidase (ACO), were found in EPA-treated groups. Surprisingly and opposite to the expectations, a very significant decrease in the expression levels of liver PPARl (P<.01) was observed after EPA treatment. These findings show the ability of EPA ethyl ester treatment to down-regulate some genes involved in fatty acid synthesis without affecting the transcriptional activation of o-oxidation-related genes.
机译:s-3脂肪酸改善脂肪代谢的确切机制尚不完全清楚。这项研究旨在确定二十碳五烯酸(EPA)乙酯给药对参与脂肪形成和脂肪酸氧化途径的几种肌肉,肝脏和脂肪组织基因表达水平的影响。每天喂饲标准饮食(对照组动物)或高脂饮食的雄性Wistar大鼠,每天用EPA乙酯(1g / kg)经口管饲法治疗5周。高脂饮食导致血浆胆固醇水平显着增加(P <.01),而EPA可以将其恢复(P <.001)。在EPA治疗组中,循环甘油三酸酯水平也显着降低(P <.05)。 EPA的使用引起某些脂肪生成基因的显着下调,例如肌肉乙酰基CoA羧化酶o(ACC o)(P <.05)和肝脂肪酸合酶(FAS)(P <.05)。此外,在饲喂对照饮食的EPA处理动物中观察到了葡萄糖激酶(GK)基因表达的下降(P <.01),而在饲喂高脂饮食的组中发现了GK mRNA水平的显着增加。另一方面,在EPA处理的组中未发现参与o-氧化的基因的改变,例如乙酰辅酶A合酶4(ACS4),乙酰辅酶A合酶5(ACS5)或乙酰辅酶A氧化酶(ACO)。出乎意料地且与预期相反,在EPA处理后观察到肝PPAR1的表达水平非常显着的降低(P <.01)。这些发现表明,EPA乙酯处理具有下调脂肪酸合成中涉及的某些基因而不影响o-氧化相关基因的转录激活的能力。

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