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足月儿和早产儿内源性合成二十二碳六烯酸(C22:6 ω-3)和花生四烯酸(C20:4 ω-6)的中间产物。

Intermediates in endogenous synthesis of C22:6 omega 3 and C20:4 omega 6 by term and preterm infants.

作者信息

Sauerwald T U, Hachey D L, Jensen C L, Chen H, Anderson R E, Heird W C

机构信息

USDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Houston, Texas 77030, USA.

出版信息

Pediatr Res. 1997 Feb;41(2):183-7. doi: 10.1203/00006450-199702000-00005.

Abstract

An alternative pathway of omega 3 and omega 6 fatty acid metabolism has been described in isolated rate hepatocytes and human fibroblasts. This alternative pathway, which is independent of delta 4 desaturation, involves elongation of C22 5 omega 3 and C22:4 omega 6 to C24 fatty acids, delta 6 desaturation of the C24 fatty acids and subsequent beta oxidation of the desaturated products to C22:6 omega 3 and C22:5 omega 6. To determine whether this alternative pathway is operative in the human infant and also to obtain additional information concerning endogenous conversion of C18:3 omega 3 and C18:2 omega 6 to longer chain more unsaturated fatty acids, presence of [M + 18] isotopomers of omega 3 and omega 6 fatty acids in the plasma phospholipid fraction of term and preterm infants after administration of [U-13C]18:3 omega 3 and [U-13C]18:2 omega 6 was determined by negative chemical ionization gas chromatography/mass spectrometry. [M + 18] isotopomers of the following omega 3 fatty acids were detected: C18:3, C18:4, C20:3, C20:4, C20:5, C22:4, C22:5, C22:6, C24:4 (two infants only), C24:5, and C24:6. [M + 18] isotopomers of omega 6 fatty acids detected included only C18:2, C18:3, C20:2, C20:3, and C20:4, but sensitivity was insufficient to detect [M + 18] isotopomers of C22 and C24 omega 6 fatty acids. Presence of [M + 18] isotopomers of C24:5 omega 3 and C24:6 omega 3 indicates that these fatty acids were synthesized endogenously from C18:3 omega 3. This plus the in vitro data strongly suggests that infants use the recently described alternative pathway in endogenous synthesis of C22:6 omega 3. However, involvement also of delta 4 desaturation cannot be excluded. Detection of [M + 18] isotopomers of C20:3 omega 3, C20:2 omega 6, and C22:4 omega 3 suggests that C18:3 omega 3, C18:2 omega 6, and C20:4 omega 3 are elongated as well as desaturated. The specific fate of these elongation products and their importance in endogenous synthesis of omega 3 and omega 6 long chain polyunsaturated fatty acids remain to be determined.

摘要

在分离的大鼠肝细胞和人成纤维细胞中,已描述了ω-3和ω-6脂肪酸代谢的另一条途径。这条独立于Δ4去饱和作用的替代途径,涉及将C22:5ω-3和C22:4ω-6延长为C24脂肪酸,C24脂肪酸的Δ6去饱和作用以及随后将去饱和产物β氧化为C22:6ω-3和C22:5ω-6。为了确定这条替代途径在人类婴儿中是否起作用,并获得有关C18:3ω-3和C18:2ω-6内源性转化为更长链、更多不饱和脂肪酸的更多信息,在给予[U-13C]18:3ω-3和[U-13C]18:2ω-6后,通过负化学电离气相色谱/质谱法测定足月和早产婴儿血浆磷脂部分中ω-3和ω-6脂肪酸的[M + 18]同位素异构体。检测到以下ω-3脂肪酸的[M + 18]同位素异构体:C18:3、C18:4、C20:3、C20:4、C20:5、C22:4、C22:5、C22:6、C24:4(仅两名婴儿)、C24:5和C24:6。检测到的ω-6脂肪酸的[M + 18]同位素异构体仅包括C18:2、C18:3、C20:2、C20:3和C20:4,但灵敏度不足以检测C22和C24ω-6脂肪酸的[M + 18]同位素异构体。C24:5ω-3和C24:6ω-3的[M + 18]同位素异构体的存在表明这些脂肪酸是由C18:3ω-3内源性合成的。这一点加上体外数据有力地表明婴儿在内源性合成C22:6ω-3时使用了最近描述的替代途径。然而,也不能排除Δ4去饱和作用的参与。C20:3ω-3、C20:2ω-6和C22:4ω-3的[M + 18]同位素异构体的检测表明C18:3ω-3、C18:2ω-6和C20:4ω-3既被延长又被去饱和。这些延长产物的具体去向及其在ω-3和ω-6长链多不饱和脂肪酸内源性合成中的重要性仍有待确定。

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