4.6 Article

PEMT, Delta 6 desaturase, and palmitoyldocosahexaenoyl phosphatidylcholine are increased in rats during pregnancy

Journal

JOURNAL OF LIPID RESEARCH
Volume 59, Issue 1, Pages 123-136

Publisher

ELSEVIER
DOI: 10.1194/jlr.M080309

Keywords

omega-3 fatty acids; phospholipids; fatty acids; nutrition/lipids; tandem mass spectrometry; microarray; liver; blood; prenatal nutritional physiological phenomena; phosphatidylethanolamine methyltransferase; 16:0/docosahexaenoic acid phosphatidylcholine

Funding

  1. Natural Sciences and Engineering Research Council of Canada [327149- 2013]
  2. Natural Sciences and Engineering Research Council of Canada
  3. Ontario Graduate Scholarship
  4. Ontario Women's Health Scholarship
  5. Canada Research Chairs program [950-228125]

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DHA is important for fetal neurodevelopment. During pregnancy, maternal plasma DHA increases, but the mechanism is not fully understood. Using rats fed a fixed-formula diet (DHA as 0.07% total energy), plasma and liver were collected for fatty acid profiling before pregnancy, at 15 and 20 days of pregnancy, and 7 days postpartum. Phosphatidylethanolamine methyltransferase (PEMT) and enzymes involved in PUFA synthesis were examined in liver. Ad hoc transcriptomic and lipidomic analyses were also performed. With pregnancy, DHA increased in liver and plasma lipids, with a large increase in plasma DHA between day 15 and day 20 that was mainly attributed to an increase in 16: 0/DHA phosphatidylcholine (PC) in liver (2 Delta 6-fold) and plasma (3.9-fold). Increased protein levels of Delta 6 desaturase (FADS2) and PEMT at day 20 and increased Pemt expression and PEMT activity at day 15 suggest that during pregnancy, both DHA synthesis and 16: 0/DHA PC synthesis are upregulated. Transcriptomic analysis revealed minor changes in the expression of genes related to phospholipid synthesis, but little insight on DHA metabolism. Hepatic PEMT appears to be the mechanism for increased plasma 16: 0/DHA PC, which is supported by increased DHA biosynthesis based on increased FADS2 protein levels.

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