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Comparison of bioavailability of krill oil versus fish oil and health effect

BACKGROUND: The aim of this review is to summarize the effects of krill oil (KO) or fish oil (FO) on eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) incorporation in plasma phospholipids or membrane of red blood cells (RBCs) as shown in human and animal studies. Furthermore, we discuss th...

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Autores principales: Ulven, Stine M, Holven, Kirsten B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559234/
https://www.ncbi.nlm.nih.gov/pubmed/26357480
http://dx.doi.org/10.2147/VHRM.S85165
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author Ulven, Stine M
Holven, Kirsten B
author_facet Ulven, Stine M
Holven, Kirsten B
author_sort Ulven, Stine M
collection PubMed
description BACKGROUND: The aim of this review is to summarize the effects of krill oil (KO) or fish oil (FO) on eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) incorporation in plasma phospholipids or membrane of red blood cells (RBCs) as shown in human and animal studies. Furthermore, we discuss the findings in relation to the possible different health effects, focusing on lipids, inflammatory markers, cardiovascular disease risk, and biological functions of these two sources of long-chain n-3 polyunsaturated fatty acids (PUFAs). METHODS: A literature search was conducted in PubMed in January 2015. In total, 113 articles were identified, but based on selection criteria, 14 original papers were included in the review. RESULTS: Studies on bioavailability of EPA and DHA from KO and FO in humans and animals are limited and the interpretation is difficult, as different amounts of EPA and DHA have been used, duration of intervention differs, and different study groups have been included. Two human studies – one postprandial study and one intervention study – used the same amount of EPA and DHA from KO or FO, and they both showed that the bioavailability of EPA and DHA from KO seems to be higher than that from FO. Limited effects of KO and FO on lipids and inflammatory markers in human and animal studies were reported. Gene expression data from animal studies showed that FO upregulated the cholesterol synthesis pathway, which was the opposite of the effect mediated by KO. KO also regulated far more metabolic pathways than FO, which may indicate different biological effects of KO and FO. CONCLUSION: There seems to be a difference in bioavailability of EPA and DHA after intake of KO and FO, but more studies are needed before a firm conclusion can be made. It is also necessary to document the beneficial health effects of KO with more human studies and to elucidate if these effects differ from those after regular fish and FO intake.
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spelling pubmed-45592342015-09-09 Comparison of bioavailability of krill oil versus fish oil and health effect Ulven, Stine M Holven, Kirsten B Vasc Health Risk Manag Review BACKGROUND: The aim of this review is to summarize the effects of krill oil (KO) or fish oil (FO) on eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) incorporation in plasma phospholipids or membrane of red blood cells (RBCs) as shown in human and animal studies. Furthermore, we discuss the findings in relation to the possible different health effects, focusing on lipids, inflammatory markers, cardiovascular disease risk, and biological functions of these two sources of long-chain n-3 polyunsaturated fatty acids (PUFAs). METHODS: A literature search was conducted in PubMed in January 2015. In total, 113 articles were identified, but based on selection criteria, 14 original papers were included in the review. RESULTS: Studies on bioavailability of EPA and DHA from KO and FO in humans and animals are limited and the interpretation is difficult, as different amounts of EPA and DHA have been used, duration of intervention differs, and different study groups have been included. Two human studies – one postprandial study and one intervention study – used the same amount of EPA and DHA from KO or FO, and they both showed that the bioavailability of EPA and DHA from KO seems to be higher than that from FO. Limited effects of KO and FO on lipids and inflammatory markers in human and animal studies were reported. Gene expression data from animal studies showed that FO upregulated the cholesterol synthesis pathway, which was the opposite of the effect mediated by KO. KO also regulated far more metabolic pathways than FO, which may indicate different biological effects of KO and FO. CONCLUSION: There seems to be a difference in bioavailability of EPA and DHA after intake of KO and FO, but more studies are needed before a firm conclusion can be made. It is also necessary to document the beneficial health effects of KO with more human studies and to elucidate if these effects differ from those after regular fish and FO intake. Dove Medical Press 2015-08-28 /pmc/articles/PMC4559234/ /pubmed/26357480 http://dx.doi.org/10.2147/VHRM.S85165 Text en © 2015 Ulven and Holven. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Ulven, Stine M
Holven, Kirsten B
Comparison of bioavailability of krill oil versus fish oil and health effect
title Comparison of bioavailability of krill oil versus fish oil and health effect
title_full Comparison of bioavailability of krill oil versus fish oil and health effect
title_fullStr Comparison of bioavailability of krill oil versus fish oil and health effect
title_full_unstemmed Comparison of bioavailability of krill oil versus fish oil and health effect
title_short Comparison of bioavailability of krill oil versus fish oil and health effect
title_sort comparison of bioavailability of krill oil versus fish oil and health effect
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559234/
https://www.ncbi.nlm.nih.gov/pubmed/26357480
http://dx.doi.org/10.2147/VHRM.S85165
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