Increases in plasma n-3 tetracosapentaenoic acid and tetracosahexaenoic acid following 12 weeks of EPA, but not DHA, supplementation in women and men

Ruxandra D. Rotarescu , Kimia Rezaei , David M. Mutch , Adam H. Metherel
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引用次数: 3

Abstract

Dietary feeding and stable isotope studies in rodents support that the 24-carbon omega-3 polyunsaturated fatty acids, tetracosapentaenoic acid (24:5n-3, TPAn-3) and tetracosahexaenoic acid (24:6n-3, THA), are immediate precursors to docosahexaenoic acid (DHA, 22:6n-3). In this study, we assessed for the first time, changes in TPAn-3 or THA levels following omega-3 PUFA supplementation in humans, providing insight into human omega-3 PUFA metabolism. In this secondary analysis of a double-blind randomized control trial, women and men (19 – 30 years, n = 10 – 14 per sex, per diet) were supplemented with 3 g/day EPA, DHA, or olive oil control for 12 weeks. Plasma TPAn-3 and THA concentrations were determined by gas chromatography-mass spectrometry to determine changes following supplementation in a sex-specific manner (sex x time). EPA supplementation significantly increased (p < 0.0001) plasma TPAn-3 by 215% (1.3 ± 0.1 – 4.1 ± 0.7, nmol/mL ± SEM) and THA by 112% (1.7 ± 0.2 – 3.6 ± 0.5, nmol/mL ± SEM). Furthermore, women had 111% and 99% higher plasma TPAn-3 and THA in the EPA supplemented group compared to men (p < 0.0001). There were no significant effects of time on plasma TPAn-3 or THA concentrations in the DHA supplemented or olive oil supplemented groups. In conclusion, EPA, but not DHA, supplementation in humans increased plasma TPAn-3 and THA levels, suggesting that THA accumulates prior to conversion to DHA in the n-3 PUFA synthesis pathway. Furthermore, women generally exhibit higher plasma TPAn-3 and THA concentrations compared with men, suggesting that women have a greater ability to accumulate 24-carbon n-3 PUFA in plasma via EPA and DPAn-3 elongation, which may explain the known higher DHA levels in women.

Summary: In this secondary analysis of a double-blind randomized control trial, we assessed changes in omega-3 (n-3) tetracosapentaenoic acid (24:5n-3, TPAn-3) and tetracosahexaenoic acid (24:6n-3, THA) plasma levels in women and men (19 – 30 years, n = 10 – 14 per sex, per diet) following 12-weeks of n-3 PUFA supplementation (3 g/day EPA, DHA or olive oil). Women had higher plasma TPAn-3 in all supplementation groups and higher THA levels in the EPA and olive oil groups (p < 0.0001) compared to men. EPA supplementation increased (p < 0.0001) plasma TPAn-3 by 215% (1.3 ± 0.1 – 4.1 ± 0.7, nmol/mL ± SEM) and THA by 112% (1.7 ± 0.2 – 3.6 ± 0.5, nmol/mL ± SEM), but DHA supplementation had no effect. For the first time in humans, we show that plasma TPAn-3 and THA levels are higher in women and increased with EPA, but not DHA supplementation, suggesting an accumulation of THA prior to conversion to DHA in the n-3 PUFA synthesis pathway.

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在补充EPA而非DHA 12周后,女性和男性血浆n-3四碳五烯酸和四碳六烯酸增加
啮齿类动物的饮食喂养和稳定同位素研究支持24碳omega-3多不饱和脂肪酸四碳五烯酸(24:5n-3, TPAn-3)和四碳六烯酸(24:6n-3, THA)是二十二碳六烯酸(DHA, 22:6n-3)的直接前体。在这项研究中,我们首次评估了人类补充omega-3 PUFA后TPAn-3或THA水平的变化,为人类omega-3 PUFA代谢提供了见解。在这项双盲随机对照试验的二次分析中,女性和男性(19 - 30岁,每个性别,每种饮食n = 10 - 14)在12周内每天补充3克EPA, DHA或橄榄油。通过气相色谱-质谱法测定血浆TPAn-3和THA浓度,以确定以性别特异性方式(性别x时间)补充后的变化。补充EPA显著提高(p <0.0001)等离子体TPAn-3 215%(1.3±0.1,4.1±0.7 nmol /毫升±SEM),那112%(1.7±0.2,3.6±0.5 nmol /毫升±SEM)。此外,与男性相比,EPA补充组女性血浆TPAn-3和THA分别高出111%和99% (p <0.0001)。在DHA补充组和橄榄油补充组中,时间对血浆TPAn-3或THA浓度没有显著影响。综上所述,人体补充EPA而非DHA会增加血浆TPAn-3和THA水平,表明THA在n-3 PUFA合成途径转化为DHA之前积累。此外,与男性相比,女性通常表现出更高的血浆TPAn-3和THA浓度,这表明女性通过EPA和DPAn-3延伸在血浆中积累24碳n-3 PUFA的能力更强,这可能解释了女性中已知的更高的DHA水平。摘要:在这项双盲随机对照试验的二次分析中,我们评估了女性和男性(19 - 30岁,每个性别,每个饮食n = 10 - 14)在补充12周n-3 PUFA (3 g/天EPA, DHA或橄榄油)后ω -3 (n-3)四碳五烯酸(24:5n-3, TPAn-3)和四碳六烯酸(24:6n-3, THA)血浆水平的变化。所有补充组的女性血浆TPAn-3水平较高,EPA组和橄榄油组的THA水平较高(p <0.0001)。EPA的补充增加了(p <0.0001)血浆TPAn-3增加215%(1.3±0.1 ~ 4.1±0.7,nmol/mL±SEM), THA增加112%(1.7±0.2 ~ 3.6±0.5,nmol/mL±SEM),而DHA补充对TPAn-3无影响。我们首次在人体中发现,女性血浆中TPAn-3和THA水平更高,并且随着EPA而不是DHA的补充而增加,这表明在n-3 PUFA合成途径中,THA在转化为DHA之前积累。
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来源期刊
Prostaglandins, leukotrienes, and essential fatty acids
Prostaglandins, leukotrienes, and essential fatty acids Clinical Biochemistry, Endocrinology, Diabetes and Metabolism
CiteScore
5.30
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审稿时长
64 days
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