Effects of Three Different Highly Purified n-3 Series Highly Unsaturated Fatty Acids on Lipid Metabolism in C57BL/KsJ-db/db Mice

Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA), were administered to C57BL/KsJ-db/db mice for 4 weeks by pair-feeding to compare their effects on lipid meta...

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Published inJournal of agricultural and food chemistry Vol. 57; no. 22; pp. 11047 - 11054
Main Authors Gotoh, Naohiro, Nagao, Koji, Onoda, Satoru, Shirouchi, Bungo, Furuya, Kenta, Nagai, Toshiharu, Mizobe, Hoyo, Ichioka, Kenji, Watanabe, Hiroyuki, Yanagita, Teruyoshi, Wada, Shun
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 25.11.2009
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ISSN0021-8561
1520-5118
1520-5118
DOI10.1021/jf9026553

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Abstract Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA), were administered to C57BL/KsJ-db/db mice for 4 weeks by pair-feeding to compare their effects on lipid metabolism and to evaluate the effects of DPA on lipid metabolism. The hepatic TG level and total amount was decreased by treatment with DHA and DPA compared to the control. The efficacy of DPA was greater than that of EPA, but less than that of DHA. In contrast, EPA had the greatest serum TG reducing effect. The hepatic cytosol fraction of the DHA-treated group contained the lowest fatty acid synthase (FAS) and malic enzyme (ME) activity levels. Furthermore, the DHA-treated group contained the highest serum adiponectin concentrations. These findings indicate that the strong hepatic TG-lowering effect of DHA is due to the suppression of TG synthesis. The same tendencies were observed in DPA-treated mice, and the effect was stronger than that observed in EPA-treated mice, but equivalent to that observed in DHA-treated mice. Based on these results, DPA possesses lipid metabolism-improving effects. The beneficial effects of DPA for lipid metabolism were not superior to those of EPA and DHA, and the effect was always intermediate between those of EPA and DHA.
AbstractList Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA), were administered to C57BL/KsJ-db/db mice for 4 weeks by pair-feeding to compare their effects on lipid metabolism and to evaluate the effects of DPA on lipid metabolism. The hepatic TG level and total amount was decreased by treatment with DHA and DPA compared to the control. The efficacy of DPA was greater than that of EPA, but less than that of DHA. In contrast, EPA had the greatest serum TG reducing effect. The hepatic cytosol fraction of the DHA-treated group contained the lowest fatty acid synthase (FAS) and malic enzyme (ME) activity levels. Furthermore, the DHA-treated group contained the highest serum adiponectin concentrations. These findings indicate that the strong hepatic TG-lowering effect of DHA is due to the suppression of TG synthesis. The same tendencies were observed in DPA-treated mice, and the effect was stronger than that observed in EPA-treated mice, but equivalent to that observed in DHA-treated mice. Based on these results, DPA possesses lipid metabolism-improving effects. The beneficial effects of DPA for lipid metabolism were not superior to those of EPA and DHA, and the effect was always intermediate between those of EPA and DHA.
Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA), were administered to C57BL/KsJ-db/db mice for 4 weeks by pair-feeding to compare their effects on lipid metabolism and to evaluate the effects of DPA on lipid metabolism. The hepatic TG level and total amount was decreased by treatment with DHA and DPA compared to the control. The efficacy of DPA was greater than that of EPA, but less than that of DHA. In contrast, EPA had the greatest serum TG reducing effect. The hepatic cytosol fraction of the DHA-treated group contained the lowest fatty acid synthase (FAS) and malic enzyme (ME) activity levels. Furthermore, the DHA-treated group contained the highest serum adiponectin concentrations. These findings indicate that the strong hepatic TG-lowering effect of DHA is due to the suppression of TG synthesis. The same tendencies were observed in DPA-treated mice, and the effect was stronger than that observed in EPA-treated mice, but equivalent to that observed in DHA-treated mice. Based on these results, DPA possesses lipid metabolism-improving effects. The beneficial effects of DPA for lipid metabolism were not superior to those of EPA and DHA, and the effect was always intermediate between those of EPA and DHA.Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA), were administered to C57BL/KsJ-db/db mice for 4 weeks by pair-feeding to compare their effects on lipid metabolism and to evaluate the effects of DPA on lipid metabolism. The hepatic TG level and total amount was decreased by treatment with DHA and DPA compared to the control. The efficacy of DPA was greater than that of EPA, but less than that of DHA. In contrast, EPA had the greatest serum TG reducing effect. The hepatic cytosol fraction of the DHA-treated group contained the lowest fatty acid synthase (FAS) and malic enzyme (ME) activity levels. Furthermore, the DHA-treated group contained the highest serum adiponectin concentrations. These findings indicate that the strong hepatic TG-lowering effect of DHA is due to the suppression of TG synthesis. The same tendencies were observed in DPA-treated mice, and the effect was stronger than that observed in EPA-treated mice, but equivalent to that observed in DHA-treated mice. Based on these results, DPA possesses lipid metabolism-improving effects. The beneficial effects of DPA for lipid metabolism were not superior to those of EPA and DHA, and the effect was always intermediate between those of EPA and DHA.
Author Nagai, Toshiharu
Ichioka, Kenji
Watanabe, Hiroyuki
Gotoh, Naohiro
Nagao, Koji
Furuya, Kenta
Yanagita, Teruyoshi
Onoda, Satoru
Wada, Shun
Mizobe, Hoyo
Shirouchi, Bungo
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  surname: Gotoh
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  email: wada@kaiyodai.ac.jp
BackLink https://www.ncbi.nlm.nih.gov/pubmed/19848389$$D View this record in MEDLINE/PubMed
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Keywords n-3 series highly unsaturated fatty acids
triglyceride
eicosapentaenoic acid
docosahexaenoic acid
docosapentaenoic acid
lipid metabolism
C57BL/KsJ-db/db mice
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SSID ssj0008570
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Snippet Triglycerides (TG) consisting of highly purified (>97%) n-3 series highly unsaturated fatty acids, eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA),...
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SubjectTerms administration & dosage
analysis
animal models
Animals
chemistry
docosahexaenoic acid
Docosahexaenoic Acids
Docosahexaenoic Acids - administration & dosage
docosapentaenoic acid
drug effects
Eicosapentaenoic Acid
Eicosapentaenoic Acid - administration & dosage
enzymology
experimental diets
Fatty Acid Synthases
Fatty Acid Synthases - analysis
Fatty Acids, Unsaturated
Fatty Acids, Unsaturated - administration & dosage
fish oils
genetics
lipid metabolism
Lipid Metabolism - drug effects
Liver
Liver - chemistry
Liver - drug effects
Liver - enzymology
Malate Dehydrogenase
Malate Dehydrogenase - analysis
Male
Mice
Mice, Inbred C57BL
Molecular Nutrition
Mutation
omega-3 fatty acids
purification
Receptors, Leptin
Receptors, Leptin - genetics
Triglycerides
Triglycerides - administration & dosage
Triglycerides - analysis
Triglycerides - chemistry
unsaturated fatty acids
Title Effects of Three Different Highly Purified n-3 Series Highly Unsaturated Fatty Acids on Lipid Metabolism in C57BL/KsJ-db/db Mice
URI http://dx.doi.org/10.1021/jf9026553
https://www.ncbi.nlm.nih.gov/pubmed/19848389
https://www.proquest.com/docview/46452143
https://www.proquest.com/docview/734145470
Volume 57
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