首页> 外文期刊>The Journal of Nutritional Biochemistry >Protective effects of dietary EPA and DHA on ischemia-reperfusion-induced intestinal stress.
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Protective effects of dietary EPA and DHA on ischemia-reperfusion-induced intestinal stress.

机译:饮食中EPA和DHA对缺血再灌注引起的肠应激的保护作用。

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摘要

The immunoregulatory effects of dietary omega-3 fatty acids are still not fully characterized. The aim of this study was to determine whether dietary eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) intake limits intestinal ischemia-reperfusion (IR) injury. To test this, rats were fed either control or EPA/DHA supplemented diet for 3 weeks following which they underwent either a sham or an IR surgical protocol. A significant reduction in mucosal damage was observed after EPA/DHA supplemented diet as reflected by maintenance of total protein content. To address the underlying mechanisms of protection, we measured parameters of oxidative stress, intestinal and serological cytokines and intestinal eicosanoids. Interestingly, EPA/DHA fed animals displayed a higher activity of oxidative stress enzyme machinery, i.e., superoxide dismutase and catalase in addition to a reduction in total nitrateitrite content. While no changes in cytokines were observed, eicosanoid analyses of intestinal tissue revealed an increase in metabolites of the 12-lipoxygenase pathway following IR. Further, IR in EPA/DHA fed animals was accompanied by a significant increase of 17,18-epoxyeicosatetraenoic acid, 8-Iso prostaglandin F3 alpha and thromboxane B3, by more than 12-, 6-, 3-fold, respectively. Thus, the data indicate that EPA/DHA supplementation may be able to reduce early intestinal IR injury by anti-oxidative and anti-inflammatory mechanisms. All rights reserved, Elsevier.
机译:饮食中的ω-3脂肪酸的免疫调节作用仍未完全表征。这项研究的目的是确定饮食二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的摄入量是否限制了肠缺血再灌注(IR)损伤。为了测试这一点,给大鼠喂食对照或补充EPA / DHA的饮食3周,然后进行假手术或IR手术方案。补充EPA / DHA的饮食后,粘膜损伤显着减少,这反映在总蛋白含量的维持上。为了解决潜在的保护机制,我们测量了氧化应激,肠道和血清细胞因子以及肠道类花生酸的参数。有趣的是,用EPA / DHA喂养的动物除了降低了总硝酸盐/亚硝酸盐含量外,还显示出较高的氧化应激酶活性,即超氧化物歧化酶和过氧化氢酶。虽然未观察到细胞因子的变化,但肠道组织的类花生酸分析显示IR后12-脂氧合酶途径的代谢产物增加。此外,在EPA / DHA喂养的动物中,IR伴随着17,18-环氧二十碳四烯酸,8-异前列腺素F 和血栓烷B 3 的显着增加。分别超过12倍,6倍和3倍。因此,数据表明,EPA / DHA补充剂可能能够通过抗氧化和抗炎机制减少早期肠道IR损伤。保留所有权利,Elsevier。

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