首页> 美国卫生研究院文献>Journal of Lipid Research >Whole-body synthesis-secretion rates of long-chain n-3 PUFAs from circulating unesterified α-linolenic acid in unanesthetized rats
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Whole-body synthesis-secretion rates of long-chain n-3 PUFAs from circulating unesterified α-linolenic acid in unanesthetized rats

机译:麻醉大鼠中循环未酯化的α-亚麻酸对长链n-3 PUFA的全身合成分泌率

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摘要

Docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA), long-chain n-3 PUFAs important for brain and heart function, can be obtained from dietary fish products or by liver synthesis from α-linolenic acid (α-LNA). Their daily human dietary requirements are not clear, and their liver synthesis rates in humans and nonhumans are unknown. We estimated whole-body (presumably liver) synthesis rates in unanesthetized rats by infusing [U-13C]α-LNA intravenously for 2 h and measuring labeled and unlabeled n-3 PUFA in arterial plasma using negative chemical ionization GC-MS. Newly synthesized esterified [13C]DHA, [13C]EPA, and [13C]docosapentaenoic acid (DPA) appeared in arterial plasma after 60 min of infusion, then their concentrations rose in an S-shaped manner. Esterified concentration × plasma volume data were fit with a sigmoidal equation, whose peak first derivatives provided synthesis rates of unlabeled EPA, DPA, and DHA equal to 8.40, 6.27, and 9.84 μmol/day, respectively. The DHA synthesis rate exceeded the published daily rat brain DHA consumption rate by 30-fold, suggesting that liver synthesis from α-LNA could maintain brain DHA homeostasis were DHA absent from the diet. This stable isotope infusion method could be used to quantify whole-body DHA synthesis rates in human subjects.
机译:二十二碳六烯酸(DHA)和二十碳五烯酸(EPA),对脑和心脏功能很重要的长链n-3 PUFA,可以从食用鱼产品中获得,也可以通过α-亚麻酸(α-LNA)的肝脏合成获得。他们的日常人类饮食需求尚不清楚,并且他们在人类和非人类中的肝脏合成率尚不清楚。我们通过静脉内注入[U- 13 C]α-LNA2 h并通过负离子测量动脉血浆中标记和未标记的n-3 PUFA来估计未麻醉大鼠的全身(大概是肝脏)合成速率化学电离GC-MS。新合成的酯化[ 13 C] DHA,[ 13 C] EPA和[ 13 C]二​​十二碳五烯酸(DPA)出现在动脉血浆中输注60分钟后,其浓度呈S形上升。酯化浓度×血浆体积数据通过S形方程拟合,该方程的峰一阶导数提供的未标记EPA,DPA和DHA的合成速率分别等于8.40、6.27和9.84μmol/天。 DHA的合成率超过了已发表的每日大鼠脑DHA消耗率的​​30倍,这表明饮食中不含DHA时,α-LNA的肝脏合成可以维持脑DHA稳态。这种稳定的同位素注入方法可用于定量人体受试者体内DHA的合成速率。

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