# Sex-Specific Changes to Brain Fatty Acids, Plasmalogen, and Plasma Endocannabinoids in Offspring Exposed to Maternal and Postnatal High-Linoleic-Acid Diets

**Authors:** Henry C. Ezechukwu, Luke J. Ney, Madeline A. Jarvis, Nirajan Shrestha, Olivia J. Holland, James S. M. Cuffe, Anthony V. Perkins, Suk-Yu Yau, Andrew J. McAinch, Deanne H. Hryciw

PMC · DOI: 10.3390/ijms25147911 · International Journal of Molecular Sciences · 2024-07-19

## TL;DR

A high-linoleic-acid diet during pregnancy and childhood affects brain fatty acids and endocannabinoids in rat offspring, with effects differing by sex.

## Contribution

This study reveals sex-specific and developmental impacts of high-linoleic-acid diets on brain fatty acid profiles and endocannabinoids in rat offspring.

## Key findings

- Postnatal high-LA diet increased docosapentaenoate in male rat offspring brains.
- Maternal high-LA diet altered multiple fatty acid concentrations in male and female offspring brains.
- Postnatal high-LA diet increased plasma endocannabinoids and testosterone in both sexes.

## Abstract

Linoleic acid (LA) is required for neuronal development. We have previously demonstrated sex-specific changes in cardiovascular and hepatic function in rat offspring from mothers consuming a high-LA diet, with some effects associated with reduced LA concentration in the postnatal diet. At this time, the impact of a high-maternal-LA diet on offspring brain development and the potential for the postnatal diet to alter any adverse changes are unknown. Rat offspring from mothers fed low- (LLA) or high-LA (HLA) diets during pregnancy and lactation were weaned at postnatal day 25 (PN25) and fed LLA or HLA diets until sacrifice in adulthood (PN180). In the offspring’s brains, the postnatal HLA diet increased docosapentaenoate in males. The maternal HLA diet increased LA, arachidonate, docosapentaenoate, C18:0 dimethylacetal (DMA), C16:0 DMA, C16:0 DMA/C16:0, and C18:0 DMA/C18:0, but decreased eoicosenoate, nervoniate, lignocerate, and oleate in males. Maternal and postnatal HLA diets reduced oleate and vaccenate and had an interaction effect on myristate, palmitoleate, and eicosapentaenoate in males. In females, maternal HLA diet increased eicosadienoate. Postnatal HLA diet increased stearate and docosapentaenoate. Maternal and postnatal HLA diets had an interaction effect on oleate, arachidate, and docosahexaenoic acid (DHA)/omega (n)-6 docosapentaenoic acid (DPA) in females. Postnatal HLA diet decreased DHA/n-6 DPA in males and females. Postnatal HLA diet increased plasma endocannabinoids (arachidonoyl ethanolamide and 2-arachidonoyl glycerol), as well as other N-acyl ethanolamides and testosterone. HLA diet alters brain fatty acids, plasma endocannabinoids, and plasmalogen concentrations in a development-specific and sex-specific manner.

## Linked entities

- **Chemicals:** linoleic acid (PubChem CID 5280450), arachidonate (PubChem CID 5460265), lignocerate (PubChem CID 5461021), oleate (PubChem CID 5460221), vaccenate (PubChem CID 5281127), myristate (PubChem CID 4075158), palmitoleate (PubChem CID 5461012), eicosapentaenoate (PubChem CID 446284), stearate (PubChem CID 5281), docosahexaenoic acid (PubChem CID 445580), arachidonoyl ethanolamide (PubChem CID 5281969), 2-arachidonoyl glycerol (PubChem CID 5282280), testosterone (PubChem CID 6013)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Chemicals:** arachidonoyl ethanolamide (MESH:C078814), Endocannabinoids (MESH:D063388), stearate (MESH:D013228), -Linoleic-Acid (MESH:D019787), DMA (MESH:C059033), C18:0 (MESH:C031183), myristate (MESH:D019814), eicosapentaenoate (MESH:D015118), DPA (MESH:C026219), oleate (MESH:D019301), Plasmalogen (MESH:D010955), testosterone (MESH:D013739), arachidonate (MESH:D016718), C16:0 (-), 2-arachidonoyl glycerol (MESH:C094503), DHA (MESH:D004281), arachidate (MESH:C094477), Fatty Acids (MESH:D005227), palmitoleate (MESH:C008757)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11277558/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC11277558/full.md

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Source: https://tomesphere.com/paper/PMC11277558