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Hepatic Cerebroside Sulfotransferase Is Induced by PPARα Activation in Mice

机译:PPARα激活小鼠肝中脑苷硫转移酶。

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摘要

Sulfatides are one of the major sphingoglycolipids in mammalian serum and are synthesized and secreted mainly from the liver as a component of lipoproteins. Recent studies revealed a protective role for serum sulfatides against arteriosclerosis and hypercoagulation. Although peroxisome proliferator-activated receptor (PPAR) α has important functions in hepatic lipoprotein metabolism, its association with sulfatides has not been investigated. In this study, sulfatide levels and the expression of enzymes related to sulfatide metabolism were examined using wild-type (+/+), Ppara-heterozygous (+/−), and Ppara-null (−/−) mice given a control diet or one containing 0.1% fenofibrate, a clinically used hypolipidemic drug and PPARα activator. Fenofibrate treatment increased serum and hepatic sulfatides in Ppara (+/+) and (+/−) mice through a marked induction of hepatic cerebroside sulfotransferase (CST), a key enzyme in sulfatide synthesis, in a PPARα-dependent manner. Furthermore, increases in CST mRNA levels were correlated with mRNA elevations of several known PPARα target genes, and such changes were not observed for other sulfatide-metabolism enzymes in the liver. These results suggest that PPARα activation enhances hepatic sulfatide synthesis via CST induction and implicate CST as a novel PPARα target gene.
机译:硫化物是哺乳动物血清中主要的鞘糖脂之一,主要从肝脏合成和分泌,作为脂蛋白的一种成分。最近的研究表明血清硫酸盐对动脉硬化和高凝有保护作用。尽管过氧化物酶体增殖物激活受体(PPAR)α在肝脂蛋白代谢中具有重要功能,但尚未研究其与硫酯的关系。在这项研究中,使用对照饮食的野生型(+ / +),Ppara-杂合子(+/-)和Ppara-null(-/-)小鼠检查了硫酸脂水平和与硫酸脂代谢相关的酶的表达。或含有0.1%非诺贝特(一种临床使用的降血脂药和PPARα激活剂)的药物。非诺贝特治疗通过以PPARα依赖性方式显着诱导肝小脑苷磺基转移酶(CST)(一种硫化物合成中的关键酶),从而增加Ppara(+ / +)和(+/-)小鼠的血清和肝硫酸盐。此外,CST mRNA水平的升高与几个已知的PPARα靶基因的mRNA升高相关,在肝脏中其他硫酸酯类代谢酶中未观察到这种变化。这些结果表明,PPARα激活通过CST诱导增强了肝硫酸酯的合成,并暗示了CST作为新的PPARα靶基因。

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