首页> 外国专利> Dietary composition comprising gamma linolenic acid a desaturase inhibitor and an arachidonic acid metabolism inhibitor for diminishing symptoms of inflammatory disorders

Dietary composition comprising gamma linolenic acid a desaturase inhibitor and an arachidonic acid metabolism inhibitor for diminishing symptoms of inflammatory disorders

机译:包含γ-亚麻酸,去饱和酶抑制剂和花生四烯酸代谢抑制剂的饮食组合物,用于减轻炎症性疾病的症状

摘要

Described are dietary strategies that will produce natural antagonists of arachidonic acid (AA) in inflammatory cells, thereby reducing the synthesis of pro-inflammatory eicosanoids, but without increasing serum levels of AA. Dietary supplements comprising gammalinoleic acid (GLA) are beneficial in treating inflammatory disease through an increase in neutrophil GLA, but there is a concomitant increase in serum AA. It has been discovered that neutrophils, the inflammatory response cells, do not possess a -5 desaturase. Thus, the product of GLA elongation, dihomogammalinoleic acid (DGLA) cannot be converted to AA and eicosanoids. However, in serum, DGLA formed from the elongation of GLA is converted to AA via the action of a -5 desaturase. This build-up of serum AA is likely to have harmful consequences in humans. For example, previous studies have demonstrated that increases in AA of this magnitude can increase platelet reactivity. Increases in sensitivity of platelets to stimuli in most cases are not desirable. Providing a -5 desaturase inhibitor has circumvented this problem, in this case, eicosapentaenoic acid (EPA) in combination with the GLA, which prevents the serum increase in AA levels upon GLA administration. Thus, there are provided herein dietary fatty acid regimens that may be used to inhibit the increase of serum arachidonic acid when GLA is provided as a dietary supplement and thereby control inflammation.
机译:描述了饮食策略,该策略将在炎性细胞中产生花生四烯酸(AA)的天然拮抗剂,从而减少促炎性类花生酸的合成,但不会增加血清AA的水平。包含γ-亚麻油酸(GLA)的膳食补充剂可通过增加中性粒细胞GLA来治疗炎性疾病,但血清AA也会随之增加。已经发现,嗜中性粒细胞,即炎症反应细胞,不具有-5去饱和酶。因此,GLA伸长率的产物二高纯亚油酸(DGLA)无法转化为AA和类花生酸。然而,在血清中,由GLA的延长形成的DGLA通过-5去饱和酶的作用转化为AA。血清AA的积累可能对人体产生有害影响。例如,先前的研究表明,AA数量级的增加可以增加血小板反应性。在大多数情况下,增加血小板对刺激的敏感性是不希望的。提供-5种去饱和酶抑制剂已经解决了这个问题,在这种情况下,二十碳五烯酸(EPA)与GLA结合使用,可防止在施用GLA后血清中AA水平的升高。因此,本文提供了膳食脂肪酸方案,当将GLA作为膳食补充剂提供时,其可以用于抑制血清花生四烯酸的增加,从而控制炎症。

著录项

  • 公开/公告号NZ506618A

    专利类型

  • 公开/公告日2003-05-30

    原文格式PDF

  • 申请/专利权人 WAKE FOREST UNIVERSITY;

    申请/专利号NZ19990506618

  • 发明设计人 CHILTON FLOYD H;

    申请日1999-02-12

  • 分类号A61K31/34;A61K31/20;

  • 国家 NZ

  • 入库时间 2022-08-22 00:01:43

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