首页> 外文期刊>The Journal of Nutritional Biochemistry >Changes in liver PPAR alpha mRNA expression in response to two levels of high-safflower-oil diets correlate with changes in adiposity and serum leptin in rats and mice.
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Changes in liver PPAR alpha mRNA expression in response to two levels of high-safflower-oil diets correlate with changes in adiposity and serum leptin in rats and mice.

机译:两种高红花油饮食对肝脏PPARαmRNA表达的变化与大鼠和小鼠肥胖和血清瘦素的变化有关。

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The ligand-dependent transcription factor peroxisome proliferator-activated receptor alpha (PPAR alpha ) is known to be activated by common fatty acids and to regulate the expression of genes of various lipid oxidation pathways and transport. High-fat diets provide more fatty acids, which presumably could enhance lipid catabolism through up-regulation of PPAR alpha signaling. However, high intake of fat could also lead to obesity. To examine PPAR alpha signaling in high-fat feeding and obesity, this study examined the hepatic mRNA expression of PPAR alpha and some of its target genes in Wistar rats and C57BL/6J mice fed two levels (20% or 30% wt/wt) of high-safflower-oil (SFO; oleic-acid-rich) diets until animals showed significantly higher body weight (13 weeks for rats and 22 weeks for mice) than those of control groups fed a 5% SFO diet. At the end of these respective feeding periods, only the rats fed 30% SFO and the mice fed 20% SFO among the two groups fed high-fat diets showed significantly higher body weight, white adipose tissue weight, serum leptin and mRNA expression of PPAR alpha (P<.05) compared to the respective control groups. Despite elevated acyl-CoA (a PPAR alpha target gene) protein and activity in both groups fed high-fat diets, the mRNA expression level of most PPAR alpha target genes examined correlated mainly to PPAR alpha mRNA levels and not to fat intake or liver lipid levels. The observation that the liver PPAR alpha mRNA expression in groups fed high-fat diets was significantly higher only in obese animals with elevated serum leptin implied that obesity and associated hyperleptinemia might have a stronger impact than dietary SFO intake per se on PPAR alpha -regulated mRNA expression in the liver..
机译:已知配体依赖性转录因子过氧化物酶体增殖物激活的受体α(PPAR alpha)被普通脂肪酸激活,并调节各种脂质氧化途径和运输基因的表达。高脂饮食提供了更多的脂肪酸,大概可以通过上调PPARα信号传导来增强脂质分解代谢。但是,高脂肪摄入也会导致肥胖。为了检查高脂喂养和肥胖症中的PPARα信号传导,本研究检查了以两种水平(20%或30%wt / wt)喂养的Wistar大鼠和C57BL / 6J小鼠中PPAR alpha及其某些靶基因的肝mRNA表达食用高红花油(SFO;富含油酸)的食物,直到动物显示出比饲喂5%SFO饮食的对照组的体重显着更高的体重(大鼠为13周,小鼠为22周)。在这些各自的进食期结束时,在高脂饮食的两组中,仅进食30%SFO的大鼠和进食20%SFO的小鼠显示出明显更高的体重,白色脂肪组织重量,血清瘦素和PPAR mRNA表达与各个对照组相比,α(P <.05)。尽管在高脂饮食中两组的酰基辅酶A(PPARα目标基因)蛋白和活性均升高,但所检查的大多数PPARα目标基因的mRNA表达水平主要与PPARαmRNA水平相关,与脂肪摄入或肝脂质无关水平。高脂饮食组肝脏PPARαmRNA表达仅在血清瘦素升高的肥胖动物中显着升高的观察结果表明,肥胖和相关的高瘦素血症可能比饮食SFO本身对PPARα调节的mRNA的影响更强在肝脏中的表达

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