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n-3多不饱和脂肪酸的过氧化抑制促炎细胞因子刺激的肝细胞中诱导型一氧化氮合酶基因表达的诱导。

Peroxidation of n-3 Polyunsaturated Fatty Acids Inhibits the Induction of iNOS Gene Expression in Proinflammatory Cytokine-Stimulated Hepatocytes.

作者信息

Araki Yoshiro, Matsumiya Miho, Matsuura Takashi, Oishi Masaharu, Kaibori Masaki, Okumura Tadayoshi, Nishizawa Mikio, Takada Hideho, Kwon A-Hon

机构信息

Department of Surgery, Kansai Medical University, 10-15 Fumizonocho, Moriguchi, Osaka 570-8506, Japan.

出版信息

J Nutr Metab. 2011;2011:374542. doi: 10.1155/2011/374542. Epub 2011 Jun 7.

Abstract

Eicosapentaenoic acid and docosahexaenoic acid (EPA/DHA), n-3 polyunsaturated fatty acids (PUFAs), have a variety of biological activities including anti-inflammatory and anticancer effects. We hypothesized that their peroxidized products contributed in part to anti-inflammatory effects. In the liver, the production of nitric oxide (NO) by inducible nitric oxide synthase (iNOS) has been implicated as one of the factors in hepatic inflammation and injury. We examined whether the peroxidation of EPA/DHA influences the induction of iNOS and NO production in proinflammatory cytokine-stimulated cultured hepatocytes, which is in vitro liver inflammation model. Peroxidized EPA/DHA inhibited the induction of iNOS and NO production in parallel with the increased levels of their peroxidation, whereas unoxidized EPA/DHA had no effects at all. Peroxidized EPA/DHA reduced the activation of transcription factor, NF-κB, and the expression of the iNOS antisense transcript, which are involved in iNOS promoter transactivation (mRNA synthesis) and its mRNA stabilization, respectively. These findings demonstrated that peroxidized products of EPA/DHA suppressed the induction of iNOS gene expression through both of the transcriptional and posttranscriptional steps, leading to the prevention of hepatic inflammation.

摘要

二十碳五烯酸和二十二碳六烯酸(EPA/DHA),即n-3多不饱和脂肪酸(PUFAs),具有多种生物活性,包括抗炎和抗癌作用。我们推测它们的过氧化产物在一定程度上促成了抗炎作用。在肝脏中,诱导型一氧化氮合酶(iNOS)产生一氧化氮(NO)被认为是肝脏炎症和损伤的因素之一。我们研究了EPA/DHA的过氧化是否会影响促炎细胞因子刺激的培养肝细胞中iNOS的诱导和NO的产生,这是一种体外肝脏炎症模型。过氧化的EPA/DHA抑制iNOS的诱导和NO的产生,且与其过氧化水平的升高平行,而未氧化的EPA/DHA则完全没有作用。过氧化的EPA/DHA降低了转录因子NF-κB的激活以及iNOS反义转录本的表达,它们分别参与iNOS启动子反式激活(mRNA合成)及其mRNA稳定性。这些发现表明,EPA/DHA的过氧化产物通过转录和转录后步骤抑制iNOS基因表达的诱导,从而预防肝脏炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3099/3136170/a9527aec79c4/JNUME2011-374542.001.jpg

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