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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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.
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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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