Placental transfer of fatty acids and fetal implications.
@article{Larqu2011PlacentalTO,
title={Placental transfer of fatty acids and fetal implications.},
author={Elvira Larqu{\'e} and Hans Demmelmair and Alfonso Gil-S{\'a}nchez and Mar{\'i}a Teresa Prieto-S{\'a}nchez and Jos{\'e} Eliseo Blanco and Ana Pag{\'a}n and Fabienne L Faber and Salvador Ventura Zamora and Juan Jos{\'e} Parrilla and Berthold V. Koletzko},
journal={The American journal of clinical nutrition},
year={2011},
volume={94 6 Suppl},
pages={
1908S-1913S
}
}Considerable amounts of long-chain polyunsaturated fatty acids (LC-PUFAs), particularly arachidonic acid and docosahexaenoic acid (DHA, 22:6n-3), are deposited in fetal tissues during pregnancy; and this process is facilitated by placental delivery. Nevertheless, the mechanisms involved in LC-PUFA placental transfer remain unclear. Stable isotope techniques have been used to study human placental fatty acid transfer in vivo. These studies have shown a significantly higher ratio of (13)C-DHA in…
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Current understanding of placental fatty acid transport
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The amount and activity of placental enzymes, receptors, and transport proteins will determine the extent of lipid transfer to the fetus that strongly contributes to fetal fat accretion, although the mechanisms are still uncertain.
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The tracer study pointed towards an impaired placental DHA uptake as a critical step, while the transfer of other 13C-FA was less affected, and the DHA transfer to the fetus was reduced in GDM pregnancies compared to controls.
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There are good indications of beneficial effects of a higher pre- or postnatal docosahexaenoic acid status on visual function and asthma risk, and Randomised clinical trials that compare different maternal or infant intakes of n-3 and n-6 fatty acids so far have not led to firm conclusions about the optimal LC-PUFA status.
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MVM FATP6 and CD36 protein expression is increased and LCPUFA are preferentially routed toward cellular storage in TG in the IUGR placenta, possibly to protect against oxidative stress associated with cellular FA accumulation.
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The decrease in placental transfer of LC-PUFAs in GDM pregnancies may constitute a possible explanation for the neurodevelopmental fetal malprogramming associated with GDM.
Intrauterine Transfer of Polyunsaturated Fatty Acids in Mother–Infant Dyads as Analyzed at Time of Delivery
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Findings may indicate that fatty acid transfer to the fetus is prioritized during gestation even during periods of maternal nutritional inadequacy.
Materno-fetal transfer of docosahexaenoic acid is impaired by gestational diabetes mellitus.
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DHA transfer to the fetus was reduced in GDM pregnancies compared with controls, which might affect the programming of neurodevelopment in their neonates.
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It is concluded that n-3 PUFA supplementation in pregnancy enhances placental accumulation of DHA and SPM precursors, does not alter placental EPA levels, and has no stimulatory effects on inflammatory gene expression.
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