Bioavailability of docosahexaenoic acid 22:6(n-3) from enantiopure triacylglycerols and their regioisomeric counterpart in rats

dc.contributor.authorLinderborg Kaisa M.
dc.contributor.authorKulkarni Amruta
dc.contributor.authorZhao Ai
dc.contributor.authorZhang Jian
dc.contributor.authorKallio Heikki
dc.contributor.authorMagnusson Johann D.
dc.contributor.authorHaraldsson Gudmundur G.
dc.contributor.authorZhang Yumei
dc.contributor.authorYang Baoru
dc.contributor.organizationfi=elintarviketieteet|en=Food Sciences|
dc.contributor.organization-code1.2.246.10.2458963.20.15178954341
dc.contributor.organization-code2610103
dc.converis.publication-id39151018
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/39151018
dc.date.accessioned2022-10-28T14:05:02Z
dc.date.available2022-10-28T14:05:02Z
dc.description.abstractLack of synthetic enantiospecific triacylglycerols (TAGs) has hindered our understanding of the impact of TAG structure on the absorption and metabolic fate of fatty acids (FAs). In a five-day feeding trial with mildly (n-3) deficient rats, the bioavailability of docosahexaenoic acid [22:6(n-3), DHA] and stearic acid (18:0) from the two different enantiomers of TAG: sn-22:6(n-3)-18:0-18:0 and sn-18:0-18:0-22:6(n-3), and their regioisomeric TAG: sn-18:0-22:6(n-3)-18:0 was compared. Less secretion of fecal DHA was detected from the sn-2 position compared with the sn-1 and sn-3 positions, but no difference was found in DHA content of the fasting plasma or in the weight of the body or organs. 18:0 was lost to feces mainly as cleaved from the primary positions but also as glycerol-bound. The 5-day intervention in rats was long enough to modify the fatty acid profile of plasma phospholipids.
dc.format.pagerange381
dc.format.pagerange389
dc.identifier.eissn1873-7072
dc.identifier.jour-issn0308-8146
dc.identifier.olddbid186163
dc.identifier.oldhandle10024/169257
dc.identifier.urihttps://www.utupub.fi/handle/11111/31917
dc.identifier.urnURN:NBN:fi-fe2021042825008
dc.language.isoen
dc.okm.affiliatedauthorLinderborg, Kaisa
dc.okm.affiliatedauthorKallio, Heikki
dc.okm.affiliatedauthorYang, Baoru
dc.okm.affiliatedauthorKulkarni, Amruta
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1016/j.foodchem.2018.12.130
dc.relation.ispartofjournalFood Chemistry
dc.relation.volume283
dc.source.identifierhttps://www.utupub.fi/handle/10024/169257
dc.titleBioavailability of docosahexaenoic acid 22:6(n-3) from enantiopure triacylglycerols and their regioisomeric counterpart in rats
dc.year.issued2019

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