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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Activation of transcription factors of nuclear factor kappa B, activator protein-1 and octamer factors in hyperalgesia.
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Activation of transcription factors of nuclear factor kappa B, activator protein-1 and octamer factors in hyperalgesia.

机译:痛觉过敏中核因子κB,激活蛋白-1和八聚体因子的转录因子的激活。

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Involvement of c-fos and neuronal nitric oxide synthase (nNOS) in the hyperalgesia induced by complete Freund adjuvant (CFA) has been reported. In this paper, we attempted to investigate whether the transcription factors regulating the gene expression of c-fos and nNOS, including activator protein-1 (AP-1), nuclear factor kappa B (NF-kappa B), and octamer factors (Oct), are activated by CFA during the development of hyperalgesia. The electrophoretic mobility shift assay (EMSA) was used to determine whether there were changes in the transcription factors in the lumbar spinal cord of adult rats following subcutaneous injection of CFA in one hindpaw of the rats. Maximum binding of AP-1, NF-kappa B and Oct was found at 0.5, 1 and 2 h after CFA injection, respectively. These findings suggest that the activation of these transcription factors is pivotal for the expression of c-Fos and nNOS proteins, which reached a peak at 3 and 48 h after CFA injection, respectively. The behavioral testing of hyperalgesia demonstrated that CFA reduced the thresholds for mechanical and thermal algesia, reaching a minimum at 6 h. The thresholds had only partially recovered after 96 h. Based on these findings, we conclude that AP-1, NF-kappa B and Oct are crucial for the expression of c-Fos proteins at an early stage (at 3 h) and for the expression of nNOS at a late stage of hyperalgesia (48 h post-injection) induced by CFA.
机译:据报道,c-fos和神经元一氧化氮合酶(nNOS)参与了完全弗氏佐剂(CFA)引起的痛觉过敏。在本文中,我们尝试研究调节c-fos和nNOS基因表达的转录因子,包括激活蛋白1(AP-1),核因子κB(NF-κB)和八聚体因子(Oct ),在痛觉过敏发生过程中被CFA激活。电泳迁移率变动分析法(EMSA)用于确定成年大鼠的腰椎皮下注射CFA后成年大鼠的腰脊髓中转录因子是否发生变化。注射CFA后分别在0.5、1和2小时发现AP-1,NF-κB和Oct的最大结合。这些发现表明,这些转录因子的激活对于c-Fos和nNOS蛋白的表达至关重要,在CFA注射后3和48 h分别达到峰值。痛觉过敏的行为测试表明,CFA降低了机械和热痛觉过敏的阈值,在6 h时达到最低。 96小时后,阈值仅部分恢复。根据这些发现,我们得出结论,AP-1,NF-κB和Oct对在痛觉过敏的早期(3小时)表达c-Fos蛋白和晚期nNOS至关重要(注射后48小时)。

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