International Journal of Molecular Sciences (Jun 2018)

Dietary Conjugated Linoleic Acid-Enriched Cheeses Influence the Levels of Circulating n-3 Highly Unsaturated Fatty Acids in Humans

  • Elisabetta Murru,
  • Gianfranca Carta,
  • Lina Cordeddu,
  • Maria Paola Melis,
  • Erika Desogus,
  • Hastimansooreh Ansar,
  • Yves Chilliard,
  • Anne Ferlay,
  • Catherine Stanton,
  • Mairéad Coakley,
  • R. Paul Ross,
  • Giovanni Piredda,
  • Margherita Addis,
  • Maria Cristina Mele,
  • Giorgio Cannelli,
  • Sebastiano Banni,
  • Claudia Manca

DOI
https://doi.org/10.3390/ijms19061730
Journal volume & issue
Vol. 19, no. 6
p. 1730

Abstract

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n-3 highly unsaturated fatty acids (n-3 HUFA) directly and indirectly regulate lipid metabolism, energy balance and the inflammatory response. We investigated changes to the n-3 HUFA score of healthy adults, induced by different types and amounts of conjugated linoleic acid (CLA)-enriched (ENCH) cheeses consumed for different periods of time, compared to dietary fish oil (FO) pills (500 mg, each containing 100 mg of eicosapentaenoic and docosahexaenoic acids—EPA+DHA) or α-linolenic acid (ALA)-rich linseed oil (4 g, containing 2 g of ALA). A significant increase in the n-3 HUFA score was observed, in a dose-dependent manner, after administration of the FO supplement. In terms of the impact on the n-3 HUFA score, the intake of ENCH cheese (90 g/day) for two or four weeks was equivalent to the administration of one or two FO pills, respectively. Conversely, the linseed oil intake did not significantly impact the n-3 HUFA score. Feeding ENCH cheeses from different sources (bovine, ovine and caprine) for two months improved the n-3 HUFA score by increasing plasma DHA, and the effect was proportional to the CLA content in the cheese. We suggest that the improved n-3 HUFA score resulting from ENCH cheese intake may be attributed to increased peroxisome proliferator-activated receptor alpha (PPAR-α) activity. This study demonstrates that natural ENCH cheese is an alternative nutritional source of n-3 HUFA in humans.

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