4.7 Article

Sex-Dependent Regulation of Placental Oleic Acid and Palmitic Acid Metabolism by Maternal Glycemia and Associations with Birthweight

期刊

出版社

MDPI
DOI: 10.3390/ijms23158685

关键词

placenta; fatty acid; lipids; beta-oxidation; fetal sex; diabetes; fetal growth

资金

  1. Singapore National Medical Research Council [NMRC/CSA-INV/0010/2016, MOH-CSAINV19nov0002]
  2. National University of Singapore
  3. National University Health System Singapore
  4. Singapore Institute for Clinical Sciences A*STAR
  5. Life Sciences Institute
  6. National University of Singapore Yong Loo Lin School of Medicine
  7. National Research Foundation [NRFI2015-05]
  8. A*STAR [IAF-ICP I1901E0040]
  9. UK Medical Research Council [MC_UU_12011/4]
  10. National Institute for Health Research (NIHR) [NF-SI-0515-10042]
  11. National Institute for Health Research (NIHR Southampton Biomedical Research Centre) [IS-BRC-1215-20004]
  12. European Union (Erasmus+ Programme ImpENSA) [598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP]
  13. Erasmus+ [598488-EPP-1-2018-1-DE-EPPKA2-CBHE-JP] Funding Source: Erasmus+
  14. National Institutes of Health Research (NIHR) [IS-BRC-1215-20004] Funding Source: National Institutes of Health Research (NIHR)

向作者/读者索取更多资源

Fetal sex influences placental lipid metabolism and may be a key factor in the impact of maternal metabolic health on perinatal outcomes.
Pregnancy complications such as maternal hyperglycemia increase perinatal mortality and morbidity, but risks are higher in males than in females. We hypothesized that fetal sex-dependent differences in placental palmitic-acid (PA) and oleic-acid (OA) metabolism influence such risks. Placental explants (n = 22) were incubated with isotope-labeled fatty acids (C-13-PA or C-13-OA) for 24 or 48 h and the production of forty-seven C-13-PA lipids and thirty-seven C-13-OA lipids quantified by LCMS. Linear regression was used to investigate associations between maternal glycemia, BMI and fetal sex with C-13 lipids, and between C-13 lipids and birthweight centile. Placental explants from females showed greater incorporation of C-13-OA and C-13-PA into almost all lipids compared to males. Fetal sex also influenced relationships with maternal glycemia, with many C-13-OA and C-13-PA acylcarnitines, C-13-PA-diacylglycerols and C-13-PA phospholipids positively associated with glycemia in females but not in males. In contrast, several C-13-OA triacylglycerols and C-13-OA phospholipids were negatively associated with glycemia in males but not in females. Birthweight centile in females was positively associated with six C-13-PA and three C-13-OA lipids (mainly acylcarnitines) and was negatively associated with eight C-13-OA lipids, while males showed few associations. Fetal sex thus influences placental lipid metabolism and could be a key modulator of the impact of maternal metabolic health on perinatal outcomes, potentially contributing toward sex-specific adaptions in which females prioritize survival.

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