4.7 Article

Physiological effects of γ-linolenic acid and sesamin on hepatic fatty acid synthesis and oxidation

Journal

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
Volume 41, Issue -, Pages 42-55

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2016.12.001

Keywords

gamma-Linolenic acid; Sesamin; Hepatic fatty acid oxidation; Hepatic fatty acid synthesis; Serum lipid levels

Funding

  1. Japan Society for the Promotion of Science [22580143]
  2. Grants-in-Aid for Scientific Research [22580143, 16K07744] Funding Source: KAKEN

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Interrelated effects of gamma-linolenic acid (GLA) and sesamin, a sesame lignan, on hepatic fatty acid synthesis and oxidation were examined. Rats were fed experimental diets supplemented with 0 or 2 g/kg sesamin (1:1 mixture of sesamin and episesamin) and containing 100 gfkg of palm oil (saturated fat), safflower oil rich in linoleic acid, or oil of evening primrose origin containing 43% GLA (GLA oil) for 18 days. In rats fed sesamin-free diets, GLA oil, compared with other oils, increased the activity and mRNA levels of various enzymes involved in fatty acid oxidation, except for some instances. Sesamin greatly increased these parameters, and the enhancing effects of sesamin on peroxisomal fatty acid oxidation rate and acyl-CoA oxidase, enoyl-CoA hydratase and acyl-CoA thioesterase activities were more exaggerated in rats fed GLA oil than in the animals fed other oils. The combination of sesamin and GLA oil also synergistically increased the mRNA levels of some peroxisomal fatty acid oxidation enzymes and of several enzymes involved in fatty acid metabolism located in other cell organelles. In the groups fed sesamin-free diets, GLA oil, compared with other oils, markedly reduced the activity and mRNA levels of various lipogenic enzymes. Sesamin reduced all these parameters, except for malic enzyme, in rats fed palm and safflower oils, but the effects were attenuated in the animals fed GLA oil. These changes by sesamin and fat type accompanied profound alterations in serum lipid levels. This may be ascribable to the changes in apolipoprotein-B-containing lipoproteins. (C) 2016 Elsevier Inc. All rights reserved.

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