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Omega-3 Phospholipids from Krill Oil Enhance Intestinal Fatty Acid Oxidation More Effectively than Omega-3 Triacylglycerols in High-Fat Diet-Fed Obese Mice

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    0532017 - FGÚ 2021 RIV CH eng J - Journal Article
    Kroupová, Petra - van Schothorst, E. M. - Keijer, J. - Bunschoten, A. - Vodička, Martin - Irodenko, Ilaria - Oseeva, Marina - Žáček, P. - Kopecký, Jan - Rossmeisl, Martin - Horáková, Olga
    Omega-3 Phospholipids from Krill Oil Enhance Intestinal Fatty Acid Oxidation More Effectively than Omega-3 Triacylglycerols in High-Fat Diet-Fed Obese Mice.
    Nutrients. Roč. 12, č. 7 (2020), č. článku 2037. E-ISSN 2072-6643
    R&D Projects: GA ČR(CZ) GA16-08124S
    Institutional support: RVO:67985823
    Keywords : krill oil * Omega-3 phospholipids * high-fat diet * Omega-3 index * small intestine
    OECD category: Endocrinology and metabolism (including diabetes, hormones)
    Impact factor: 5.719, year: 2020
    Method of publishing: Open access
    https://www.mdpi.com/2072-6643/12/7/2037

    Antisteatotic effects of omega-3 fatty acids (Omega-3) in obese rodents seem to vary depending on the lipid form of their administration. Whether these effects could reflect changes in intestinal metabolism is unknown. Here, we compare Omega-3-containing phospholipids (krill oil, omega 3PL-H) and triacylglycerols (omega 3TG) in terms of their effects on morphology, gene expression and fatty acid (FA) oxidation in the small intestine. Male C57BL/6N mice were fed for 8 weeks with a high-fat diet (HFD) alone or supplemented with 30 mg/g diet of omega 3TG or omega 3PL-H. Omega-3 index, reflecting the bioavailability of Omega-3, reached 12.5% and 7.5% in the omega 3PL-H and omega 3TG groups, respectively. Compared to HFD mice, omega 3PL-H but not omega 3TG animals had lower body weight gain (-40%), mesenteric adipose tissue (-43%), and hepatic lipid content (-64%). The highest number and expression level of regulated intestinal genes was observed in omega 3PL-H mice. The expression of FA omega-oxidation genes was enhanced in both Omega-3-supplemented groups, but gene expression within the FA beta-oxidation pathway and functional palmitate oxidation in the proximal ileum was significantly increased only in omega 3PL-H mice. In conclusion, enhanced intestinal FA oxidation could contribute to the strong antisteatotic effects of Omega-3 when administered as phospholipids to dietary obese mice.
    Permanent Link: http://hdl.handle.net/11104/0310622

     
     
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