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首页> 外文期刊>Biological & pharmaceutical bulletin >Effects of Perfluorinated Fatty Acids with Different Carbon Chain Length on Fatty Acid Profiles of Hepatic Lipids in Mice
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Effects of Perfluorinated Fatty Acids with Different Carbon Chain Length on Fatty Acid Profiles of Hepatic Lipids in Mice

机译:不同碳链长的全氟脂肪酸对小鼠肝脂质脂肪酸谱的影响

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Alterations by perfluorinated fatty acids (PFCAs) with a chain length of 6-9 carbons in the fatty acid profile of hepatic lipids of mice were investigated. The characteristic changes caused by all the PFCAs examined were increases in the contents and proportions of oleic acid (18: 1), palmitoleic acid (16: 1) and 8,11,14-eicosatrienoic acid (20: 3) in hepatic lipids. Hepatic contents of palmitic acid were also increased by the treatments with the PFCAs. These effects were almost dependent on the hepatic concentrations of PFCA molecules regardless of their carbon chain length. Perfluorooctanoic acid elevated the expressions of mRNA encoding acetyl-CoA carboxylase, fatty acid synthase, malic enzyme, stearoyl-CoA desaturase (SCD) (SCD1 and 2), chain elongase (ELOVL5), Delta 6 desaturase (Fads2), 1-acylglycerophosphocholine acyltransferase (LPCAT) (LPCAT3). The four PFCAs examined induced microsomal SCD and LPCAT in hepatic concentration-dependent manners regardless of carbon chain length. One linear regression line was confirmed between LPCAT activity and hepatic concentration of PFCA at wide range of the concentration, whereas the induction of SCD was saturable at relatively low concentration of PFCAs. These results suggest (i) that PFCAs with a chain length of 6-9 carbons change the fatty acid profile of hepatic lipids by increasing contents and proportions of 16: 1, 18: 1 and 20 : 3, (ii) that these alterations in fatty acid profile are caused by up-regulation of SCD, de nova fatty acid synthesis, chain elongase and Delta 6 desaturase and (iii) that the mechanism underlying SCD induction is, in part, mediated through peroxisome proli-erator-activated receptor alpha.
机译:研究了小鼠肝脂质的脂肪酸谱中链长为6-9个碳原子的全氟化脂肪酸(PFCA)的变化。由所有检测到的PFCA引起的特征变化是肝脂质中油酸(18:1),棕榈油酸(16:1)和8,11,14-二十碳三烯酸(20:3)的含量和比例增加。 PFCA处理也增加了棕榈酸的肝含量。这些影响几乎取决于PFCA分子的肝脏浓度,无论其碳链长度如何。全氟辛酸可提高编码乙酰辅酶A羧化酶,脂肪酸合酶,苹果酸酶,硬脂酰辅酶A去饱和酶(SCD1和2),链延长酶(ELOVL5),Delta 6去饱和酶(Fads2),1-酰基甘油磷酸胆碱酰基转移酶的mRNA表达(LPCAT)(LPCAT3)。四个PFCA均以肝脏浓度依赖性方式检测了诱导的微粒体SCD和LPCAT,而与碳链长度无关。在很宽的浓度范围内,在LPCAT活性和PFCA的肝脏浓度之间证实了一条线性回归线,而在相对较低的PFCAs浓度下,SCD的诱导是饱和的。这些结果表明(i)链长为6-9个碳的PFCA通过增加16:1、18:1和20:3的含量和比例来改变肝脂质的脂肪酸谱,(ii)这些改变脂肪酸谱是由SCD的上调,新脂肪酸合成,链延长酶和Delta 6去饱和酶引起的,以及(iii)SCD诱导的机制部分是通过过氧化物酶体增生激活的受体α介导的。

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