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鱼油通过调节 TNF-α 和 resolvins 减轻大鼠持续性炎症痛。

Fish oil attenuates persistent inflammatory pain in rats through modulation of TNF-α and resolvins.

机构信息

LabEnzInd; Departamento de Fármacos e Medicamentos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro RJ 21941-902, Brazil; Programa de Pós-Graduação em Ciências Farmacêuticas (PPGCF), Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro RJ 21941-902, Brazil.

LEFEx, Departamento de Biotecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro RJ 21941-902, Brazil; Programa de Pós-Graduação em Farmacologia e Química Medicinal (PPGFQM), Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro RJ 21941-902, Brazil.

出版信息

Life Sci. 2016 May 1;152:30-7. doi: 10.1016/j.lfs.2016.03.034. Epub 2016 Mar 21.

Abstract

UNLABELLED

Fish oil (FO), source of omega-3 fatty acids (FA), has been widely studied in the treatment of inflammatory diseases and inflammatory pain (IP). Omega-3 FA give rise to eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids, metabolized to eicosanoids and converted to resolvins with important anti-inflammatory action.

AIMS

This study investigates the effects of oral doses of omega-3 FA from FO and concentrated fish oil (CFO) in a model of sub-chronic IP, induced by Complete Freund's Adjuvant (CFA).

MAIN METHODS

IP was induced by intraplantar injection of CFA into the right hind paw of Wistar rats. Three groups were pre-treated with omega-3 FA: two groups received CFO (460mg of EPA/360mg of DHA and 690mg of EPA/540mg of DHA) and one group received natural FO (460mg EPA/300mg DHA), for 7days before IP induction (pre-treatment) and 5days after induction (treatment).

KEY FINDINGS

TNF-α levels were reduced by CFO 690 (67.9%; p<0.01), CFO 460 (57.7%; p<0.01), FO 460 (26.2%), compared to the augment promoted by CFA (549.7%; p<0.001). Resolvin levels were increased in treated groups with respect to the CFA control group (CFO 690=3196.3%, p<0.01; CFO 460=3347.1%, p<0.01; FO=1653.5%).

SIGNIFICANCE

The results indicate that the tested doses reduced inflammatory pain effectively in a short pre-treatment period, through modulation of TNF-α and resolvins and that CFO presented better results than FO. Therefore, Ω-3 FA from FO can be proposed for use as complementary medicine in the treatment of painful and inflammatory diseases.

摘要

未加标签

鱼油(FO)是 ω-3 脂肪酸(FA)的来源,已广泛研究用于治疗炎症性疾病和炎症性疼痛(IP)。 ω-3 FA 生成二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)酸,代谢为类二十烷酸,并转化为具有重要抗炎作用的 resolvins。

目的

本研究调查了口服 ω-3 FA 剂量的鱼油(FO)和浓缩鱼油(CFO)在完全弗氏佐剂(CFA)诱导的亚慢性 IP 模型中的作用。

主要方法

通过向 Wistar 大鼠右后爪足底内注射 CFA 诱导 IP。三组用 ω-3 FA 预处理:两组接受 CFO(460mg EPA/360mg DHA 和 690mg EPA/540mg DHA),一组接受天然 FO(460mg EPA/300mg DHA),在 IP 诱导前 7 天(预处理)和诱导后 5 天(治疗)。

主要发现

与 CFA 诱导的增加相比,CFO 690(67.9%;p<0.01)、CFO 460(57.7%;p<0.01)和 FO 460(26.2%)降低了 TNF-α 水平。与 CFA 对照组相比,治疗组的 resolvin 水平升高(CFO 690=3196.3%,p<0.01;CFO 460=3347.1%,p<0.01;FO=1653.5%)。

意义

结果表明,在短的预处理期内,测试剂量通过调节 TNF-α 和 resolvin 有效减轻了炎症性疼痛,并且 CFO 比 FO 效果更好。因此,FO 中的 Ω-3 FA 可作为治疗疼痛和炎症性疾病的补充药物。

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