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膳食中花生四烯酸与二十碳五烯酸对体内类花生酸生成的拮抗关系。

Antithetic relationship of dietary arachidonic acid and eicosapentaenoic acid on eicosanoid production in vivo.

作者信息

Li B, Birdwell C, Whelan J

机构信息

Department of Nutrition, University of Tennessee, Knoxville 37996-1900.

出版信息

J Lipid Res. 1994 Oct;35(10):1869-77.

PMID:7852864
Abstract

Eicosanoids are oxidative derivatives of arachidonic acid. When produced in excessive amounts, many are proinflammatory and/or prothrombotic agents. N-3 polyunsaturated fatty acids (PUFA) have been used to attenuate tissue arachidonic acid (AA, 20:4 n-6) levels and thus modulate eicosanoid production. However, there is growing evidence that dietary arachidonic acid may also be able to modulate eicosanoid formation by enriching tissue phospholipids with AA. Therefore, the effects of dietary AA and n-3 PUFA are in diametric opposition. This study investigates the antithetic relationship of dietary AA and eicosapentaenoic acid (EPA, 20:5 n-3) on fatty acid composition of hepatic phospholipids and eicosanoid production in vivo. Forty-nine CD-1 male mice were randomly divided into four dietary groups. Identical diets were supplemented with ethyl esters (1.5% w/w) of the following fatty acids: oleic acid (OA, 18:1 n-9), AA, EPA or AA+EPA. After 4 weeks on diet, peritoneal cells were stimulated in vivo with opsonized zymosan and the peritoneal exudates were analyzed for eicosanoid production (PGE2, 6-keto-PGF1 alpha, TXB2, LTB4, LTE4, and LTE5). Hepatic phospholipids were enriched with AA when AA was included in the diet, and EPA was enriched at the expense of AA when EPA was added to the diet. However, when AA was added to the diet containing equivalent amounts of EPA (AA+EPA), any effect EPA had on modulating hepatic phospholipid fatty acid composition was almost completely eliminated. Similar effects were observed with eicosanoid production. The pooled eicosanoid production in the AA group was 41% and 300% higher compared to the OA (control) and EPA groups, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

类二十烷酸是花生四烯酸的氧化衍生物。当大量产生时,许多类二十烷酸是促炎和/或促血栓形成剂。n-3多不饱和脂肪酸(PUFA)已被用于降低组织中花生四烯酸(AA,20:4 n-6)的水平,从而调节类二十烷酸的产生。然而,越来越多的证据表明,膳食中的花生四烯酸也可能通过用AA丰富组织磷脂来调节类二十烷酸的形成。因此,膳食AA和n-3 PUFA的作用是截然相反的。本研究调查了膳食AA和二十碳五烯酸(EPA,20:5 n-3)对体内肝磷脂脂肪酸组成和类二十烷酸产生的相反关系。49只CD-1雄性小鼠被随机分为四个饮食组。相同的饮食中添加了以下脂肪酸的乙酯(1.5% w/w):油酸(OA,18:1 n-9)、AA、EPA或AA+EPA。饮食4周后,用调理酵母聚糖在体内刺激腹膜细胞,并分析腹膜渗出液中的类二十烷酸产生情况(前列腺素E2、6-酮-前列腺素F1α、血栓素B2、白三烯B4、白三烯E4和白三烯E5)。当饮食中包含AA时,肝磷脂富含AA;当饮食中添加EPA时,EPA以AA为代价而富集。然而,当将AA添加到含有等量EPA的饮食中(AA+EPA)时,EPA对调节肝磷脂脂肪酸组成的任何作用几乎完全消除。在类二十烷酸产生方面也观察到了类似的效果。AA组类二十烷酸的总产生量分别比OA(对照)组和EPA组高41%和300%。(摘要截选至250字)

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