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High-Fat Feeding in Time-Dependent Manner Affects Metabolic Routes Leading to Nervonic Acid Synthesis in NAFLD

机译:随时间变化的方式高脂喂养会影响导致NAFLD中神经酸合成的代谢途径

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摘要

Nonalcoholic fatty liver disease (NAFLD) is characterized by excessive lipid accumulation in the liver. The disturbances in the fatty acid composition of stored lipids are more important than the lipid species itself, which may influence the overall effect caused by these molecules. Thus, uncovering time-dependent changes in the fatty acid composition of accumulated lipid fractions after a high fat diet seems to be a new marker of NAFLD occurrence. The experiments were conducted on high fat fed Wistar rats. The blood and liver samples were collected at the end of each experimental week and used to assess the content of lipid fractions and their fatty acid composition by gas liquid chromatography. The expression of proteins from lipid metabolism pathways and of fatty acid exporting proteins were detected by Western blotting. In the same high fat feeding period, decreased de novo lipogenesis, increased β-oxidation and lipid efflux were demonstrated. The observed effects may be the first liver protective mechanisms against lipotoxicity. Nevertheless, such effects were still not sufficient to prevent the liver from proinflammatory lipid accumulation. Moreover, the changes in liver metabolic pathways caused the plasma nervonic acid concentration in sphingomyelin to decrease simultaneously with NAFLD development, which may be a steatosis occurrence prognostic marker.
机译:非酒精性脂肪肝疾病(NAFLD)的特征是肝脏中脂质过多积聚。所储存脂质的脂肪酸组成的紊乱比脂质种类本身更为重要,这可能会影响这些分子引起的整体效果。因此,发现高脂饮食后累积脂质部分的脂肪酸组成随时间的变化似乎是NAFLD发生的新标志。实验是在高脂喂养的Wistar大鼠上进行的。在每个实验周结束时收集血液和肝脏样品,并通过气相色谱法评估脂质部分的含量及其脂肪酸组成。通过Western印迹检测脂质代谢途径中蛋白质的表达和脂肪酸输出蛋白质的表达。在相同的高脂肪喂养期,新脂肪生成减少,β-氧化增加和脂质外排被证明。观察到的效果可能是抗脂毒性的第一个肝脏保护机制。然而,这种作用仍不足以防止肝脏促炎性脂质蓄积。此外,肝脏代谢途径的改变导致鞘磷脂中的血浆神经酸浓度与NAFLD的发展同时降低,这可能是脂肪变性发生的预后标志物。

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