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. 2023 Apr;67(8):e2200479.
doi: 10.1002/mnfr.202200479. Epub 2023 Mar 8.

Effect of Gestational Fish Oil Supplementation on Liver Metabolism and Mitochondria of Male and Female Rat Offspring Programmed by Maternal High-Fat Diet

Jessika Geisebel Oliveira Neto  1 , Juliana Woyames  1 , Cherley Borba Vieira Andrade  1 , Mariana Macedo de Almeida  1 , Larissa Brito Fassarella  1 , Georgia Correia Atella  2 , Christina Maeda Takyia  1 , Isis Hara Trevenzoli  1 , Carmen Cabanelas Pazos-Moura  1
Affiliations

Effect of Gestational Fish Oil Supplementation on Liver Metabolism and Mitochondria of Male and Female Rat Offspring Programmed by Maternal High-Fat Diet

Jessika Geisebel Oliveira Neto et al. Mol Nutr Food Res. 2023 Apr.

Abstract

Scope: Perinatal maternal moderately high-fat diet (mHFD) is associated with obesity and fatty liver disease in offspring, and maternal fish oil (FO: n-3 PUFA source) supplementation may attenuate these disorders. This study evaluates the effects of FO given to pregnant rats fed a mHFD on the offspring's liver at weaning.

Methods and results: Female Wistar rats receive an isoenergetic, control (CT: 10.9% from fat) or high-fat (HF: 28.7% from fat) diet before mating, and throughout pregnancy and lactation. FO supplementation (HFFO: 2.9% of FO in the HF diet) is given to one subgroup of HF dams during pregnancy. At weaning, male and female mHFD offspring display higher body mass, adiposity, and hepatic cellular damage, steatosis, and inflammation, accompanied by increased damaged mitochondria. FO does not protect pups from systemic metabolic alterations and partially mitigates hepatic histological damage induced by mHFD only in females. However, FO reduces mRNA expression of lipogenic genes, and mitochondrial damage, and modified mitochondrial morphology suggestive of early adaptations via mitochondrial dynamics.

Conclusions: Gestational FO supplementation has limited beneficial effects on the damage caused by perinatal mHFD consumption in offspring's liver at weaning. However, FO imprinting effect on lipid metabolism and mitochondria may have beneficial long-term outcomes.

Keywords: PUFA; liver damage; metabolic programming; mitochondria; sexual dimorfism.

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