Unknown,Transcriptomics,Genomics,Proteomics

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Hepatic transcriptome of mice fed high fat diets containing palm or linseed oil


ABSTRACT: The beneficial effects of dietary long-chain (LC) n-3 polyunsaturated fatty acids (PUFA) in the prevention and/or treatment of some metabolic disorders result largely from their capacity to regulate the transcription level of many genes involved in metabolic and physiological homeostasis, especially in the liver. In this respect, they are known to bind and activate the Peroxisome Proliferator-Activated Receptor alpha (PPARalpha). The precursor of LC-PUFA, a-linoleic acid (ALA, C18:3 n-3) share some beneficial metabolic effects with its LC derivatives, however its role in gene regulation is poorly documented. Here, we analysed the hepatic transcriptome of mice fed for 5 weeks diets rich in either saturated FA from palm oil (PALM group) or ALA from linseed oil (LIN group). This modification of dietary fatty acid composition in a context of a high fat diet had a subtle but significant effect on the hepatic transcriptome. We identified mainly a group of genes that were upregulated in the LIN vs the PALM group and that include several well-known PPARalpha target genes involved in lipid and xenobiotic metabolism. Liver gene expression was measured in male C57BL/6J mice fed during 5 weeks a high fat diet (51% energy from fat) containing palm oil, rich in saturated fatty acids (n=10) or linseed oil, rich in 18:3 n-3 (n=8)

ORGANISM(S): Mus musculus

SUBMITTER: Pascal Martin 

PROVIDER: E-GEOD-73290 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

NO synthesis from arginine is favored by α-linolenic acid in mice fed a high-fat diet.

Hermier Dominique D   Guelzim Najoua N   Martin Pascal G P PG   Huneau Jean-François JF   Mathé Véronique V   Quignard-Boulangé Annie A   Lasserre Frédéric F   Mariotti François F  

Amino acids 20160513 9


Alterations in NO availability and signaling play a pivotal role at early stages of the metabolic syndrome (MetSynd). We hypothesized that dietary α-linolenic acid (ALA, 18:3 n-3) favors NO availability by modulating amino acid metabolism, with a specific impact on the arginine-NO pathway. Mice were fed a hyperlipidic diet (285 g lipid/kg, 51.1 % energy), rich in either saturated fatty acids (SFA, provided by palm oil, PALM group) or ALA (provided by linseed oil, LIN group). We measured whole-bo  ...[more]

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