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Impact of maternal undernutrition around the time of conception on factors regulating hepatic lipid metabolism and microRNAs in singleton and twin fetuses

机译:受孕前后母亲营养不良对单胎和双胎胎儿肝脏脂质代谢和microRNA调控因子的影响

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摘要

We have investigated the effects of embryo number and maternal undernutrition imposed either around the time of conception or before implantation on hepatic lipid metabolism in the sheep fetus. We have demonstrated that periconceptional undernutrition and preimplantation undernutrition each resulted in decreased hepatic fatty acid β-oxidation regulators, PGC-1α (P < 0.05), PDK2 (P < 0.01), and PDK4 (P < 0.01) mRNA expression in singleton and twin fetuses at 135–138 days gestation. In singletons, there was also lower hepatic PDK4 (P < 0.01), CPT-1 (P < 0.01), and PKCζ (P < 0.01) protein abundance in the PCUN and PIUN groups and a lower protein abundance of PDPK-1 (P < 0.05) in the PCUN group. Interestingly, in twins, the hepatic protein abundance of p-AMPK (Ser485) (P < 0.01), p-PDPK-1 (Ser41) (P < 0.05), and PKCζ (P < 0.05) was higher in the PCUN and PIUN groups, and hepatic PDK4 (P < 0.001) and CPT-1 (P < 0.05) protein abundance was also higher in the PIUN twin fetus. We also found that the expression of a number of microRNAs was altered in response to PCUN or PIUN and that there is evidence that these changes may underlie the changes in the protein abundance of key regulators of hepatic fatty acid β-oxidation in the PCUN and PIUN groups. Therefore, embryo number and the timing of maternal undernutrition in early pregnancy have a differential impact on hepatic microRNA expression and on the factors that regulate hepatic fatty acid oxidation and lipid synthesis.
机译:我们已经研究了受孕前后或植入前胚胎数目和母体营养不足对绵羊胎儿肝脂质代谢的影响。我们已经证明,围生期的营养不足和植入前的营养不足都会导致肝脂肪酸β-氧化调节因子,PGC-1α(P <0.05),PDK2(P <0.01)和PDK4(P <0.01)mRNA在单胎和双胎中的表达降低。妊娠135-138天的胎儿。在单胎中,PCUN和PIUN组中的肝PDK4(P <0.01),CPT-1(P <0.01)和PKCζ(P <0.01)蛋白含量较低,而PDPK-1(P <0.05)在PCUN组中。有趣的是,在双胞胎中,p-AMPK(Ser 485 )(P <0.01),p-PDPK-1(Ser 41 )的肝蛋白丰度(P <0.05 ),PCUN和PIUN组的PKCζ(P <0.05)较高,而PIUN双胎胎儿的肝PDK4(P <0.001)和CPT-1(P <0.05)蛋白丰度也较高。我们还发现,响应于PCUN或PIUN,许多microRNA的表达发生了变化,并且有证据表明这些变化可能是PCUN和PIUN中肝脏脂肪酸β-氧化的关键调节因子蛋白质丰度变化的基础。组。因此,妊娠早期的胚胎数量和母体营养不良的时机对肝脏microRNA表达以及调节肝脏脂肪酸氧化和脂质合成的因素有不同的影响。

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