Literature DB >> 29167412

PEMT, Δ6 desaturase, and palmitoyldocosahexaenoyl phosphatidylcholine are increased in rats during pregnancy.

Alan Chalil1, Alex P Kitson1, Juan J Aristizabal Henao1, Kristin A Marks1, Jason L Elzinga1, Daniel M E Lamontagne-Kam1, Daniel Chalil1, Flavia Badoud2, David M Mutch2, Ken D Stark3.   

Abstract

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 (2.6-fold) and plasma (3.9-fold). Increased protein levels of Δ6 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.
Copyright © 2018 by the American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

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

Mesh:

Substances:

Year:  2017        PMID: 29167412      PMCID: PMC5748503          DOI: 10.1194/jlr.M080309

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  51 in total

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