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首页> 外文期刊>Molecular and Cellular Biochemistry >Effect of dietary saturated fatty acids on HNF-4α DNA binding activity and ApoCIII mRNA in sedentary rat liver
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Effect of dietary saturated fatty acids on HNF-4α DNA binding activity and ApoCIII mRNA in sedentary rat liver

机译:日粮饱和脂肪酸对久坐大鼠肝脏HNF-4αDNA结合活性和ApoCIII mRNA的影响

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Hind limb-suspended rats represent a sedentary-hyperinsulinemic model with a liver dyslipidemia mainly related to changes in sterol regulatory element-binding protein 1 (SREBP-1) and peroxisome proliferator-activated receptor-α (PPARα) expression and activity. To assess the effects of dietary fatty acids on hepatic lipid homeostasis, the hepatic expression and activity of PPARα, SREBP-1, and hepatocyte nuclear factor-4α (HNF-4α) were investigated in this animal model. In control and sedentary rats, diets enriched with saturated, monounsaturated, and polyunsaturated fatty acids (PUFA) enhanced the expression of the PPARα target genes carnitine palmitoyltransferase 1 and acyl-CoA oxidase, the highest effect being exerted by ω-3. The same diets reduced SREBP-1 mRNA and target lipogenic gene expression, as indicated by the reduction in fatty acid synthase and acetyl-CoA carboxylase mRNA content. Effects were greater in sedentary rat liver than in controls on the same diet. Only the ω-3 enriched diet decreased liver triglyceride content as well as plasma cholesterol and triglyceride levels in sedentary rats. This effect may be mainly related to the enhanced mitochondrial and peroxisomal β-oxidation genes expression. On the other hand, saturated fatty acid-enriched diet induced an increase in liver triglyceride content and enhanced plasma cholesterol and triglyceride levels, both in control and immobilized rats. This detrimental effect may be ascribed to the induced HNF-4α binding activity on ApoCIII promoter and to the enhanced ApoCIII mRNA levels both in control and in sedentary rat livers. In conclusion, we can speculate that dietary saturated fats, acting at apolipoprotein transcriptional level, may impact on the close relationship existing among high ApoCIII plasma level, dyslipidemia, and atherosclerosis.
机译:后肢悬吊的大鼠代表久坐性高胰岛素血症模型,其肝血脂异常主要与固醇调节元件结合蛋白1(SREBP-1)和过氧化物酶体增殖物激活受体-α(PPARα)的表达和活性有关。为了评估膳食脂肪酸对肝脂质稳态的影响,在该动物模型中研究了肝中PPARα,SREBP-1和肝细胞核因子4α(HNF-4α)的表达和活性。在对照组和久坐的大鼠中,富含饱和,单不饱和和多不饱和脂肪酸(PUFA)的饮食可提高PPARα目标基因肉碱棕榈酰转移酶1和酰基辅酶A氧化酶的表达,其中ω-3发挥了最大作用。相同的饮食减少了SREBP-1 mRNA和目标脂肪基因的表达,如脂肪酸合酶和乙酰辅酶A羧化酶mRNA含量的减少所表明的。在相同饮食条件下,久坐大鼠肝脏的影响大于对照组。只有富含ω-3的饮食可以减少久坐大鼠的肝脏甘油三酸酯含量以及血浆胆固醇和甘油三酸酯水平。该作用可能主要与线粒体和过氧化物酶体β-氧化基因表达增强有关。另一方面,在对照组和固定化大鼠中,富含饱和脂肪酸的饮食都导致肝脏甘油三酸酯含量增加,血浆胆固醇和甘油三酸酯水平升高。这种有害作用可能归因于在对照和久坐的大鼠肝脏中诱导的对ApoCIII启动子的HNF-4α结合活性和增强的ApoCIII mRNA水平。总之,我们可以推测,膳食饱和脂肪以载脂蛋白的转录水平起作用,可能影响高ApoCIII血浆水平,血脂异常和动脉粥样硬化之间存在的密切关系。

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