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对新生儿口服13C-U-18:2n-6和2H5-20:3n-6后血浆中13C和2H标记的n-6脂肪酸进行的房室分析。

Compartmental analyses of plasma 13C- and 2H-labeled n-6 fatty acids arising from oral administrations of 13C-U-18:2n-6 and 2H5-20:3n-6 in newborn infants.

作者信息

Pawlosky Robert J, Lin Yu Hong, Llanos Adolfo, Mena Patricia, Uauy Ricardo, Salem Norman

机构信息

Laboratory of Metabolic Control, National Institutes on Alcohol Abuse & Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Pediatr Res. 2006 Sep;60(3):327-33. doi: 10.1203/01.pdr.0000232782.09352.ef. Epub 2006 Jul 20.

DOI:10.1203/01.pdr.0000232782.09352.ef
PMID:16857777
Abstract

Efficacy of (13)C-U-18:2n-6 and (2)H(5)-20:3n-6 toward synthesis of labeled-20:4n-6 was studied in newborn infants utilizing compartmental models of plasma labeled n-6 fatty acids (FA). Ten infants received oral doses of (13)C-U-18:2n-6 and (2)H(5)-20:3n-6 ethyl esters (100 and 2 mg/kg, respectively). Rate constant coefficients and half-lives (t((1/2))) of n-6 FA were determined from the time-course concentrations of labeled-FA. Plasma n-6 FA values approximated steady state concentrations. Synthetic and utilization rates were calculated. Eight percent (range, 2-21%) of plasma (13)C-U-18:2n-6 was used for synthesis of (13)C-18:3n-6, -20:2n-6, and -20:3n-6. Seventy percent of (13)C-20:3n-6 (mean, CV: 0.26) was available for synthesis of (13)C-20:4n-6. The percentage of (2)H(5)-20:3n-6 converted to (2)H(5)-20:4n-6 was lower (mean: 26%, p < 0.02) than the (13)C-labeled analogue. Turnover of 18:2n-6 in subjects and of 20:4n-6 in plasma was 4.2 g/kg/d (CV: 0.58) and 4.3 mg/kg/d (CV: 0.81), respectively. Intake of 18:2n-6 and 20:4n-6 were estimated to be 3.0 g/kg/d (+/-1.7) and 2.8 mg/kg/d (+/- 2.2), respectively. Infants required additional 18:2n-6 and 20:4n-6 (mean: 1.2 g and 1.5 mg/kg/d) above predicted intake amounts to maintain plasma concentrations of 18:2n-6 and 20:4n-6, in order to spare FA from fat stores.

摘要

利用血浆标记n-6脂肪酸(FA)的房室模型,研究了(13)C-U-18:2n-6和(2)H(5)-20:3n-6对新生儿合成标记-20:4n-6的功效。十名婴儿分别口服了(13)C-U-18:2n-6和(2)H(5)-20:3n-6乙酯(分别为100和2mg/kg)。根据标记FA的时间进程浓度确定n-6 FA的速率常数系数和半衰期(t(1/2))。血浆n-6 FA值接近稳态浓度。计算了合成和利用率。8%(范围为2-21%)的血浆(13)C-U-18:2n-6用于合成(13)C-18:3n-6、-20:2n-6和-20:3n-6。70%的(13)C-20:3n-6(平均值,CV:0.26)可用于合成(13)C-20:4n-6。(2)H(5)-20:3n-6转化为(2)H(5)-20:4n-6的百分比低于(13)C标记的类似物(平均值:26%,p<0.02)。受试者体内18:2n-6和血浆中20:4n-6的周转率分别为4.2g/kg/d(CV:0.58)和4.3mg/kg/d(CV:0.81)。估计18:2n-6和20:4n-6的摄入量分别为3.0g/kg/d(±1.7)和2.8mg/kg/d(±2.2)。婴儿需要比预测摄入量额外摄入18:2n-6和20:4n-6(平均值:1.2g和1.5mg/kg/d),以维持血浆中18:2n-6和2:4n-6的浓度,从而从脂肪储存中节省FA。

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