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甲草胺和西维因通过不同程度地抑制核因子κB的激活来抑制脂多糖诱导的诱导型一氧化氮合酶的表达。

Alachlor and carbaryl suppress lipopolysaccharide-induced iNOS expression by differentially inhibiting NF-kappaB activation.

作者信息

Shimomura-Shimizu Mifumi, Sugiyama Kei-ichi, Muroi Masashi, Tanamoto Ken-ichi

机构信息

Division of Microbiology, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan.

出版信息

Biochem Biophys Res Commun. 2005 Jul 8;332(3):793-9. doi: 10.1016/j.bbrc.2005.05.024.

Abstract

Nitric oxide (NO) produced by macrophages plays an important role in host defense and inflammation. We found that two agrochemicals, alachlor and carbaryl, inhibit lipopolysaccharide (LPS)-induced NO production by macrophages. In the present study, we investigated this inhibitory mechanism in RAW 264 cells. Both chemicals inhibited LPS-induced iNOS protein and mRNA expression as well as murine iNOS promoter activity. When treating these chemicals with reducing agents, the inhibition by carbaryl was reversed, but not the inhibition by alachlor. These chemicals also inhibited LPS-induced interferon-beta (IFN-beta) expression, an indispensable factor for LPS-induced iNOS expression. The inhibited iNOS expression, however, was not restored by exogenous IFN-beta supplementation. LPS-induced nuclear translocation of NF-kappaB, which is necessary for the expression of IFN-beta and iNOS, was inhibited by these chemicals: however, the LPS-induced degradation of IkappaB-alpha and IkappaB-beta was inhibited only by alachlor. These results indicate that alachlor and carbaryl differentially impair the LPS-induced NF-kappaB activation, leading to the inhibition of NO production.

摘要

巨噬细胞产生的一氧化氮(NO)在宿主防御和炎症中发挥重要作用。我们发现两种农用化学品,甲草胺和西维因,可抑制巨噬细胞中脂多糖(LPS)诱导的NO产生。在本研究中,我们在RAW 264细胞中研究了这种抑制机制。两种化学品均抑制LPS诱导的诱导型一氧化氮合酶(iNOS)蛋白和mRNA表达以及小鼠iNOS启动子活性。当用还原剂处理这些化学品时,西维因的抑制作用被逆转,但甲草胺的抑制作用未被逆转。这些化学品还抑制LPS诱导的干扰素-β(IFN-β)表达,这是LPS诱导iNOS表达所必需的因子。然而,通过外源性补充IFN-β并不能恢复被抑制的iNOS表达。这些化学品抑制了LPS诱导的NF-κB核转位,而NF-κB核转位是IFN-β和iNOS表达所必需的:然而,LPS诱导的IκB-α和IκB-β降解仅被甲草胺抑制。这些结果表明,甲草胺和西维因对LPS诱导的NF-κB激活的损害不同,从而导致NO产生受到抑制。

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