Suppr超能文献

几何和位置脂肪酸异构体在培养的胶质瘤细胞中与亚油酸和亚麻酸的去饱和及延长反应不同。

Geometric and positional fatty acid isomers interact differently with desaturation and elongation of linoleic and linolenic acids in cultured glioma cells.

作者信息

Cook H W, Emken E A

机构信息

Department of Pediatrics, Dalhousie University, Halifax, N.S., Canada.

出版信息

Biochem Cell Biol. 1990 Mar;68(3):653-60. doi: 10.1139/o90-094.

Abstract

A range of geometrical and positional isomers of 18-carbon acyl chains are potential components of diets containing fats from processed vegetable oils or ruminant animals. We have examined seventeen 18-carbon fatty acids, with cis or trans double bonds in positions 8-15, for their effects on desaturation and chain elongation of [1-14C]18:2(n-6) or [1-14C]18:3(n-3), primarily to 20:4(n-6) or 20:5(n-3) respectively, in cultured glioma cells. All trans monoenoic positional isomers inhibited delta 5 desaturation by approximately 60% when 18:2(n-6) was the substrate, with no positional discrimination evident; with 18:3(n-3) as substrate, only the 11- and 12-trans isomers were effective inhibitors of formation of 20:5(n-3). All cis positional monoene isomers, except for 12-cis 18:1, produced 25-30% inhibition of conversion of 18:2(n-6) to 20:4(n-6), but had little effect on the conversion of 18:3(n-3) to 20:5(n-3). For dienoic isomers, the presence of a 12-trans bond inhibited formation of both 20:4(n-6) and 20:5(n-3) and this was enhanced markedly when the other bond in the dienoic acid was 9-trans. Presence of a 9-trans or 15-trans bond with 12-cis gave little effect except for a slight inhibition of 20:4(n-6) formation by the 12-cis,15-trans 18:2 isomer. All-cis 20:3(n-9) blocked delta 5 desaturation, increasing 20:3(n-6) accumulation from 18:2(n-6) and suggesting that formation of 20:3(n-9) from 18:1(n-9) during essential fatty acid deficiency may further exacerbate the already compromised formation of 20:4(n-6). Further, the differential effects of various cis and trans isomers on the metabolism of 18:2(n-6) and 18:3(n-3) suggest that either delta 5 desaturation is not common in both pathways of conversion of 18:2(n-6) or 18:3(n-3) to their primary products or that selective interactions of trans and cis isomers occur when the essential fatty acid substrates are different.

摘要

18碳酰基链的一系列几何异构体和位置异构体是含有加工植物油或反刍动物脂肪的饮食中的潜在成分。我们研究了17种在8-15位带有顺式或反式双键的18碳脂肪酸,观察它们对培养的胶质瘤细胞中[1-14C]18:2(n-6)或[1-14C]18:3(n-3)去饱和及链延长的影响,主要是分别转化为20:4(n-6)或20:5(n-3)。当以18:2(n-6)为底物时,所有反式单烯位置异构体均抑制Δ5去饱和约60%,且无明显位置选择性;以18:3(n-3)为底物时,只有11-反式和12-反式异构体是20:5(n-3)形成的有效抑制剂。除12-顺式18:1外,所有顺式位置单烯异构体对18:2(n-6)转化为20:4(n-6)有25%-30%的抑制作用,但对18:3(n-3)转化为20:5(n-3)影响很小。对于二烯异构体,12-反式键的存在抑制20:4(n-6)和20:5(n-3)的形成,当二烯酸中的另一个键为9-反式时,这种抑制作用显著增强。9-反式或15-反式键与12-顺式键同时存在时,除12-顺式、15-反式18:2异构体对20:4(n-6)形成有轻微抑制外,几乎没有影响。全顺式20:3(n-9)阻断Δ5去饱和,增加18:2(n-6)生成20:3(n-6)的积累,这表明在必需脂肪酸缺乏期间由18:1(n-9)生成20:3(n-9)可能会进一步加剧本已受损的20:4(n-6)的形成。此外,各种顺式和反式异构体对18:2(n-6)和18:3(n-3)代谢的不同影响表明,要么在18:2(n-6)或18:3(n-3)转化为其主要产物的两条途径中Δ5去饱和并不常见,要么当必需脂肪酸底物不同时,反式和顺式异构体之间存在选择性相互作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验