AI Article Synopsis

  • The study examines how the number of embryos and maternal undernutrition around conception or before implantation affect liver fat metabolism in sheep fetuses.
  • It reveals that undernutrition leads to decreased expression of key regulators for fat breakdown in both singleton and twin fetuses, but with different protein levels depending on embryo number.
  • The research also highlights changes in microRNA expression, suggesting that both embryo number and timing of maternal undernutrition significantly influence liver fat metabolism mechanisms in developing sheep fetuses.

Article Abstract

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 (Ser(485)) (P < 0.01), p-PDPK-1 (Ser(41)) (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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719029PMC
http://dx.doi.org/10.1152/ajpendo.00600.2014DOI Listing

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