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非酯化脂肪酸激活氧化应激介导的核因子κB信号通路,以诱导犊牛肝细胞发生炎症反应。

NEFAs activate the oxidative stress-mediated NF-κB signaling pathway to induce inflammatory response in calf hepatocytes.

作者信息

Shi Xiaoxia, Li Dangdang, Deng Qinghua, Li Yu, Sun Guoquan, Yuan Xue, Song Yuxiang, Wang Zhe, Li Xiaobing, Li Xinwei, Liu Guowen

机构信息

Key Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, 5333 Xi'an Road, Changchun 130062, Jilin, China.

College of Animal Science and Technology, Inner Mongolia National University, Tongliao 028042, China.

出版信息

J Steroid Biochem Mol Biol. 2015 Jan;145:103-12. doi: 10.1016/j.jsbmb.2014.10.014. Epub 2014 Oct 22.

Abstract

Non-esterified fatty acids (NEFAs) are important induction factors of inflammatory responses in some metabolic diseases. High plasma levels of NEFAs and oxidative stress exist in the dairy cows with ketosis. The aim of this study was to investigate whether high levels of NEFAs can induce inflammatory response and the specific molecular mechanism in the hepatocytes of dairy cow. In vitro, primary cultured bovine hepatocytes were treated with different concentrations of NEFAs, PDTC (an NF-κB inhibitor) and NAC (an antioxidant). NEFAs significantly activated NF-κB pathway. Activated NF-κB upregulated the release of pro-inflammatory cytokines, thereby inducing inflammatory response in bovine hepatocytes. When PDTC was added, activation of NF-κB-mediated inflammatory response induced by NEFAs was inhibited. NEFAs treatment results in the overproduction of the markers of oxidative stress, reactive oxygen species (ROS) and malondialdehyde (MDA), which were ameliorated by NAC treatment. These increased ROS and MDA were caused by decreasing activity of antioxidant system, including glutathione peroxidase, superoxide dismutase and catalase, in bovine hepatocytes treated with NEFAs. NAC also ameliorated NEFAs-mediated NF-κB activation and the release of pro-inflammatory cytokines. These results indicate that high concentrations of NEFAs can induce cattle hepatocytes inflammatory response through activating the oxidative stress-mediated NF-κB signaling pathway.

摘要

非酯化脂肪酸(NEFAs)是某些代谢性疾病中炎症反应的重要诱导因子。酮病奶牛存在血浆NEFAs水平升高和氧化应激现象。本研究旨在探讨高水平的NEFAs是否能诱导奶牛肝细胞的炎症反应及其具体分子机制。在体外,用不同浓度的NEFAs、PDTC(一种NF-κB抑制剂)和NAC(一种抗氧化剂)处理原代培养的牛肝细胞。NEFAs显著激活NF-κB通路。激活的NF-κB上调促炎细胞因子的释放,从而诱导牛肝细胞的炎症反应。当加入PDTC时,NEFAs诱导的NF-κB介导的炎症反应被抑制。NEFAs处理导致氧化应激标志物活性氧(ROS)和丙二醛(MDA)的过量产生,NAC处理可改善这种情况。在用NEFAs处理的牛肝细胞中,这些增加的ROS和MDA是由抗氧化系统(包括谷胱甘肽过氧化物酶、超氧化物歧化酶和过氧化氢酶)活性降低引起的。NAC还改善了NEFAs介导的NF-κB激活和促炎细胞因子的释放。这些结果表明,高浓度的NEFAs可通过激活氧化应激介导的NF-κB信号通路诱导牛肝细胞炎症反应。

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