首页> 外文期刊>Biochemical and Biophysical Research Communications >Constitutive omega-3 fatty acid production in fat-1 transgenic mice and docosahexaenoic acid administration to wild type mice protect against 2,4,6-trinitrobenzene sulfonic acid-induced colitis
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Constitutive omega-3 fatty acid production in fat-1 transgenic mice and docosahexaenoic acid administration to wild type mice protect against 2,4,6-trinitrobenzene sulfonic acid-induced colitis

机译:脂肪-1转基因小鼠和十二碳六甲酸给予野生型小鼠的组成型ω-3脂肪酸产生防止2,4,6-三硝基苯磺酸诱导的结肠炎

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摘要

Omega-3 (omega-3) polyunsaturated fatty acids (PUFAs) are known to have strong anti-inflammatory effects. In the present study, we investigated the protective effects of omega-3 PUFAs on experimentally induced murine colitis. Intrarectal administration of 2.5% 2,4,6-trinitrobenzene sulfonic acid (TNBS) caused inflammation in the colon of wild type mice, but this was less severe in fat-1 transgenic mice that constitutively produce omega-3 PUFAs from w-6 PUFAs. The intraperitoneal administration of docosahexaenoic acid (DHA), a representative omega-3 PUFA, was also protective against TNBS-induced murine colitis. In addition, endogenously formed and exogenously introduced omega-3 PUFAs attenuated the production of malondialdehyde and 4-hydroxynonenal in the colon of TNBS-treated mice. The effective protection against inflammatory and oxidative colonic tissue damages in fat-1 and DHA-treated mice was associated with suppression of NF-kappa B activation and cyclooxygenase-2 expression and with elevated activation of Nrf2 and upregulation of its target gene, heme oxygenise-1. Taken together, these results provide mechanistic basis of protective action of omega-3 fatty PUFAs against experimental colitis. (C) 2017 Published by Elsevier Inc.
机译:已知ω-3(OMEGA-3)多不饱和脂肪酸(PUFA)具有强烈的抗炎作用。在本研究中,我们研究了OMEGA-3 PUFA对实验诱导的鼠结肠炎的保护作用。在野生型小鼠的结肠中引起2.5%2,4,6-三硝基苯磺酸(TNB)的内部给药,但在脂肪-1转基因小鼠中,这对来自W-6 PUFA的ω-3 PUFA的脂肪-1转基因小鼠中的炎症不太严重。腹腔内给予二十二碳甲酸(DHA),代表性ω-3 Pufa,对TNBS诱导的小鼠结肠炎进行了保护。此外,内源性形成和外源地引入OMEGA-3 PUFA衰减在TNBS处理的小鼠的结肠中产生丙二醛和4-羟基诺的生产。对脂肪-1和DHA处理的小鼠的炎症和氧化结肠组织损伤的有效保护与NF-κB活化和环加氧酶-2表达的抑制相关,并升高了NRF2的活化和其靶基因的上调,血红素氧式 - 1。总之,这些结果为欧米茄-3脂肪毒性PUFA对实验性结肠炎的保护作用提供机械基础。 (c)2017年由elsevier公司发布

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