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Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight
BACKGROUND: Fetal docosahexaenoic acid (DHA) supply relies on preferential transplacental transfer, which is regulated by placental DHA lipid metabolism. Maternal hyperglycemia and obesity associate with higher birthweight and fetal DHA insufficiency but the role of placental DHA metabolism is uncle...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349043/ https://www.ncbi.nlm.nih.gov/pubmed/34362294 http://dx.doi.org/10.1186/s10020-021-00344-w |
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author | Watkins, Oliver C. Selvam, Preben Appukuttan Pillai, Reshma Cracknell-Hazra, Victoria K. B. Yong, Hannah E. J. Sharma, Neha Cazenave-Gassiot, Amaury Bendt, Anne K. Godfrey, Keith M. Lewis, Rohan M. Wenk, Markus R. Chan, Shiao-Yng |
author_facet | Watkins, Oliver C. Selvam, Preben Appukuttan Pillai, Reshma Cracknell-Hazra, Victoria K. B. Yong, Hannah E. J. Sharma, Neha Cazenave-Gassiot, Amaury Bendt, Anne K. Godfrey, Keith M. Lewis, Rohan M. Wenk, Markus R. Chan, Shiao-Yng |
author_sort | Watkins, Oliver C. |
collection | PubMed |
description | BACKGROUND: Fetal docosahexaenoic acid (DHA) supply relies on preferential transplacental transfer, which is regulated by placental DHA lipid metabolism. Maternal hyperglycemia and obesity associate with higher birthweight and fetal DHA insufficiency but the role of placental DHA metabolism is unclear. METHODS: Explants from 17 term placenta were incubated with (13)C-labeled DHA for 48 h, at 5 or 10 mmol/L glucose treatment, and the production of 17 individual newly synthesized (13)C-DHA labeled lipids quantified by liquid chromatography mass spectrometry. RESULTS: Maternal BMI positively associated with (13)C-DHA-labeled diacylglycerols, triacylglycerols, lysophospholipids, phosphatidylcholine and phosphatidylethanolamine plasmalogens, while maternal fasting glycemia positively associated with five (13)C-DHA triacylglycerols. In turn, (13)C-DHA-labeled phospholipids and triacylglycerols positively associated with birthweight centile. In-vitro glucose treatment increased most (13)C-DHA-lipids, but decreased (13)C-DHA phosphatidylethanolamine plasmalogens. However, with increasing maternal BMI, the magnitude of the glucose treatment induced increase in (13)C-DHA phosphatidylcholine and (13)C-DHA lysophospholipids was curtailed, with further decline in (13)C-DHA phosphatidylethanolamine plasmalogens. Conversely, with increasing birthweight centile glucose treatment induced increases in (13)C-DHA triacylglycerols were exaggerated, while glucose treatment induced decreases in (13)C-DHA phosphatidylethanolamine plasmalogens were diminished. CONCLUSIONS: Maternal BMI and glycemia increased the production of different placental DHA lipids implying impact on different metabolic pathways. Glucose-induced elevation in placental DHA metabolism is moderated with higher maternal BMI. In turn, findings of associations between many DHA lipids with birthweight suggest that BMI and glycemia promote fetal growth partly through changes in placental DHA metabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10020-021-00344-w. |
format | Online Article Text |
id | pubmed-8349043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83490432021-08-09 Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight Watkins, Oliver C. Selvam, Preben Appukuttan Pillai, Reshma Cracknell-Hazra, Victoria K. B. Yong, Hannah E. J. Sharma, Neha Cazenave-Gassiot, Amaury Bendt, Anne K. Godfrey, Keith M. Lewis, Rohan M. Wenk, Markus R. Chan, Shiao-Yng Mol Med Research Article BACKGROUND: Fetal docosahexaenoic acid (DHA) supply relies on preferential transplacental transfer, which is regulated by placental DHA lipid metabolism. Maternal hyperglycemia and obesity associate with higher birthweight and fetal DHA insufficiency but the role of placental DHA metabolism is unclear. METHODS: Explants from 17 term placenta were incubated with (13)C-labeled DHA for 48 h, at 5 or 10 mmol/L glucose treatment, and the production of 17 individual newly synthesized (13)C-DHA labeled lipids quantified by liquid chromatography mass spectrometry. RESULTS: Maternal BMI positively associated with (13)C-DHA-labeled diacylglycerols, triacylglycerols, lysophospholipids, phosphatidylcholine and phosphatidylethanolamine plasmalogens, while maternal fasting glycemia positively associated with five (13)C-DHA triacylglycerols. In turn, (13)C-DHA-labeled phospholipids and triacylglycerols positively associated with birthweight centile. In-vitro glucose treatment increased most (13)C-DHA-lipids, but decreased (13)C-DHA phosphatidylethanolamine plasmalogens. However, with increasing maternal BMI, the magnitude of the glucose treatment induced increase in (13)C-DHA phosphatidylcholine and (13)C-DHA lysophospholipids was curtailed, with further decline in (13)C-DHA phosphatidylethanolamine plasmalogens. Conversely, with increasing birthweight centile glucose treatment induced increases in (13)C-DHA triacylglycerols were exaggerated, while glucose treatment induced decreases in (13)C-DHA phosphatidylethanolamine plasmalogens were diminished. CONCLUSIONS: Maternal BMI and glycemia increased the production of different placental DHA lipids implying impact on different metabolic pathways. Glucose-induced elevation in placental DHA metabolism is moderated with higher maternal BMI. In turn, findings of associations between many DHA lipids with birthweight suggest that BMI and glycemia promote fetal growth partly through changes in placental DHA metabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10020-021-00344-w. BioMed Central 2021-08-06 /pmc/articles/PMC8349043/ /pubmed/34362294 http://dx.doi.org/10.1186/s10020-021-00344-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Watkins, Oliver C. Selvam, Preben Appukuttan Pillai, Reshma Cracknell-Hazra, Victoria K. B. Yong, Hannah E. J. Sharma, Neha Cazenave-Gassiot, Amaury Bendt, Anne K. Godfrey, Keith M. Lewis, Rohan M. Wenk, Markus R. Chan, Shiao-Yng Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title | Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title_full | Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title_fullStr | Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title_full_unstemmed | Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title_short | Placental (13)C-DHA metabolism and relationship with maternal BMI, glycemia and birthweight |
title_sort | placental (13)c-dha metabolism and relationship with maternal bmi, glycemia and birthweight |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349043/ https://www.ncbi.nlm.nih.gov/pubmed/34362294 http://dx.doi.org/10.1186/s10020-021-00344-w |
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