
pmid: 12576509
High fat intake is associated with fat mass gain through fatty acid activation of peroxisome proliferator-activated receptors delta and gamma, which promote adipogenesis. We show herein that, compared to a combination of specific agonists to both receptors or to saturated, monounsaturated, and omega-3 polyunsaturated fatty acids, arachidonic acid (C20:4, omega-6) promoted substantially the differentiation of clonal preadipocytes. This effect was blocked by cyclooxygenase inhibitors and mimicked by carbacyclin, suggesting a role for the prostacyclin receptor and activation of the cyclic AMP-dependent pathways that regulate the expression of the CCAAT enhancer binding proteins beta and delta implicated in adipogenesis. During the pregnancy-lactation period, mother mice were fed either a high-fat diet rich in linoleic acid, a precursor of arachidonic acid (LO diet), or the same isocaloric diet enriched in linoleic acid and alpha-linolenic acid (LO/LL diet). Body weight from weaning onwards, fat mass, epididymal fat pad weight, and adipocyte size at 8 weeks of age were higher with LO diet than with LO/LL diet. In contrast, prostacyclin receptor-deficient mice fed either diet were similar in this respect, indicating that the prostacyclin signaling contributes to adipose tissue development. These results raise the issue of the high content of linoleic acid of i) ingested lipids during pregnancy and lactation, and ii) formula milk and infant foods in relation to the epidemic of childhood obesity.
MESH: Signal Transduction, Male, Cytoplasmic and Nuclear, Receptors, Cytoplasmic and Nuclear, Inbred C57BL, Biochemistry, Mice, MESH: Pregnancy, Pregnancy, Receptors, MESH: Receptors, Cyclic AMP, MESH: Animals, [SDV.BDD]Life Sciences [q-bio]/Development Biology, MESH: Cyclic AMP, Omega-6, Mice, Knockout, Arachidonic Acid, Fatty Acids, Biologie du développement, pregnancy-lactation, Cell Differentiation, MESH: Transcription Factors, Development Biology, MESH: Fatty Acids, Adipose Tissue, MESH: Dietary Fats, prostacyclin receptor-deficient mice, Female, childhood obesity, MESH: Adipose Tissue, Signal Transduction, MESH: Cell Differentiation, Knockout, 610, QD415-436, MESH: Epoprostenol, Receptors, Epoprostenol, adipogenesis, Fatty Acids, Omega-6, [SDV.BDD] Life Sciences [q-bio]/Development Biology, Animals, Humans, MESH: Mice, Adipose Tissue;Animals;Arachidonic Acid;Body Weight;Cell Differentiation;Cyclic AMP;Dietary Fats;Epoprostenol;Fatty Acids;Omega-6;Female;Fibroblasts;Humans;Male;Mice;Inbred C57BL;Knockout;Pregnancy;Receptors;Cytoplasmic and Nuclear;Signal Transduction;Transcription Factors, MESH: Humans, Body Weight, Fibroblasts, Dietary Fats, Epoprostenol, MESH: Male, MESH: Arachidonic Acid, MESH: Body Weight, Mice, Inbred C57BL, MESH: Fibroblasts, MESH: Female, Transcription Factors
MESH: Signal Transduction, Male, Cytoplasmic and Nuclear, Receptors, Cytoplasmic and Nuclear, Inbred C57BL, Biochemistry, Mice, MESH: Pregnancy, Pregnancy, Receptors, MESH: Receptors, Cyclic AMP, MESH: Animals, [SDV.BDD]Life Sciences [q-bio]/Development Biology, MESH: Cyclic AMP, Omega-6, Mice, Knockout, Arachidonic Acid, Fatty Acids, Biologie du développement, pregnancy-lactation, Cell Differentiation, MESH: Transcription Factors, Development Biology, MESH: Fatty Acids, Adipose Tissue, MESH: Dietary Fats, prostacyclin receptor-deficient mice, Female, childhood obesity, MESH: Adipose Tissue, Signal Transduction, MESH: Cell Differentiation, Knockout, 610, QD415-436, MESH: Epoprostenol, Receptors, Epoprostenol, adipogenesis, Fatty Acids, Omega-6, [SDV.BDD] Life Sciences [q-bio]/Development Biology, Animals, Humans, MESH: Mice, Adipose Tissue;Animals;Arachidonic Acid;Body Weight;Cell Differentiation;Cyclic AMP;Dietary Fats;Epoprostenol;Fatty Acids;Omega-6;Female;Fibroblasts;Humans;Male;Mice;Inbred C57BL;Knockout;Pregnancy;Receptors;Cytoplasmic and Nuclear;Signal Transduction;Transcription Factors, MESH: Humans, Body Weight, Fibroblasts, Dietary Fats, Epoprostenol, MESH: Male, MESH: Arachidonic Acid, MESH: Body Weight, Mice, Inbred C57BL, MESH: Fibroblasts, MESH: Female, Transcription Factors
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