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首页> 外文期刊>Lipids >Increased lipid synthesis and decreased β-oxidation in the liver of SHR/NDmcr-cp (cp/cp) rats, an animal model of metabolic syndrome
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Increased lipid synthesis and decreased β-oxidation in the liver of SHR/NDmcr-cp (cp/cp) rats, an animal model of metabolic syndrome

机译:SHR / NDmcr-cp(cp / cp)大鼠(代谢综合征的动物模型)肝脏中脂质合成的增加和β氧化的减少

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摘要

SHR/NDmcr-cp (cp/cp) rats (SHR/NDcp) are an animal model of metabolic syndrome. A previous study of ours revealed drastic increases in the mass of palmitic (16:0), oleic (18:1n-9), palmitoleic (16:1n-7), cis-vaccenic (18:1n-7) and 5,8,11-eicosatrienoic acids in the liver of SHR/NDcp. However, detailed information on the class of lipid accumulated and the mechanism responsible for the overproduction of the accumulated lipid in the liver was not obtained. This study aimed to characterize the class of lipid accumulated and to explore the mechanism underlying the lipid accumulation in the liver of SHR/NDcp, in comparison with SHR/NDmcr-cp (+/+) (lean hypertensive littermates of SHR/NDcp) and Wistar Kyoto rats. In the liver of SHR/NDcp, de novo synthesis of fatty acids (16:0, 18:1n-9 and 16:1n-7) and triacylglycerol (TAG) synthesis were up-regulated and fatty acid β-oxidation was down-regulated. These perturbations of lipid metabolism caused fat accumulation in hepatocytes and accumulation of TAG, which were enriched with 16:0, 18:1n-9 and 16:1n-7, in the liver of SHR/NDcp. On the other hand, no changes were found in hepatic contents of diacylglycerol and unesterified fatty acid (FFA); among FFA, there were no differences in the hepatic concentrations of unesterified 16:0 and stearic acid between SHR/NDcp and two other groups of rats. Moreover, little change was brought about in the expression of genes responsive to endoplasmic reticulum stress in the liver of SHR/NDcp. These results may reinforce the pathophysiological role of stearoyl-CoA desaturase 1 and fatty acid elongase 6 in the liver of SHR/NDcp.
机译:SHR / NDmcr-cp(cp / cp)大鼠(SHR / NDcp)是代谢综合征的动物模型。我们先前的研究显示,棕榈酸(16:0),油酸(18:1n-9),棕榈油酸(16:1n-7),顺式-vaccenic(18:1n-7)和5的质量急剧增加SHR / NDcp肝脏中的8,11-二十碳三烯酸。但是,没有获得有关脂质堆积类别和肝脏中脂质累积过量产生机理的详细信息。与SHR / NDmcr-cp(+ / +)(SHR / NDcp的瘦高胆固醇同窝仔)相比,本研究旨在表征SHR / NDcp肝脏中脂质积累的类别并探讨其脂质积累的机制。 Wistar京都老鼠。在SHR / NDcp的肝脏中,从头合成脂肪酸(16:0、18:1n-9和16:1n-7)和三酰甘油(TAG)的合成上调,而脂肪酸β-氧化的下调规范的。这些脂类代谢的扰动导致SHR / NDcp肝脏中肝细胞中脂肪积累和TAG积累,TAG富集了16:0、18:1n-9和16:1n-7。另一方面,未发现二酰基甘油和未酯化脂肪酸(FFA)的肝脏含量发生变化;在FFA中,SHR / NDcp与其他两组大鼠的未酯化16:0和硬脂酸的肝浓度没有差异。此外,在SHR / NDcp的肝脏中,响应内质网应激的基因表达几乎没有变化。这些结果可能会增强SHR / NDcp肝脏中硬脂酰CoA去饱和酶1和脂肪酸延伸酶6的病理生理作用。

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