Suppr超能文献

对乙酰氨基酚诱导的肝毒性与核因子-κB(NF-κB)和核因子白细胞介素6(NF-IL6)DNA结合活性的早期变化有关。

Acetaminophen-induced hepatotoxicity is associated with early changes in NF-kB and NF-IL6 DNA binding activity.

作者信息

Blazka M E, Germolec D R, Simeonova P, Bruccoleri A, Pennypacker K R, Luster M I

机构信息

Environmental Immunology and Neurobiology Section, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.

出版信息

J Inflamm. 1995;47(3):138-50.

PMID:9117441
Abstract

Nuclear transcription factors, such as NF-kB and NF-IL6, are believed to play an important role in regulating the expression of genes that encode for products involved in tissue damage and inflammation and, thus, may represent early biomarkers for chemical toxicities. In the present study changes in DNA binding activity of these factors were examined in livers of mice administered hepatotoxic doses of acetaminophen (APAP). NF-kB and NF-IL6 DNA binding occurred constitutively in control mouse liver. However, within 4 hr following administration of hepatotoxic doses of APAP, their binding activities were transiently lost and is in contrast to AP-1 transcription factor where activation occurs under similar conditions. These changes corresponded with increased release of inflammatory mediators (IL-6, serum amyloid A) and increased levels of enzymatic markers of hepatocyte damage. Similarly, treatment of mice with gadolinium chloride, an inhibitor of Kupffer cell activation and known to protect against APAP-induced hepatotoxicity, reduced the observed pathophysiological response in the liver while altering the APAP-associated changes in NF-kB DNA binding activity. NF-kB was found predominantly in parenchymal and endothelial cells and was composed primarily of relatively inactive p50 homodimer subunits in control liver. Taken together, these studies suggest that hepatotoxicity is associated with early and complex changes in DNA binding activities of specific transcription factors. In particular, NF-kB and NF-IL6 may serve as negative regulators of hepatocyte-derived inflammatory mediators and is analogous to that previously observed in certain other cell systems such as B lymphocytes.

摘要

核转录因子,如核因子-κB(NF-κB)和核因子白细胞介素6(NF-IL6),被认为在调节编码参与组织损伤和炎症的产物的基因表达中起重要作用,因此可能是化学毒性的早期生物标志物。在本研究中,检测了给予肝毒性剂量对乙酰氨基酚(APAP)的小鼠肝脏中这些因子的DNA结合活性变化。NF-κB和NF-IL6的DNA结合在对照小鼠肝脏中组成性存在。然而,在给予肝毒性剂量的APAP后4小时内,它们的结合活性短暂丧失,这与在类似条件下发生激活的AP-1转录因子形成对比。这些变化与炎症介质(白细胞介素6、血清淀粉样蛋白A)释放增加以及肝细胞损伤酶标志物水平升高相对应。同样,用氯化钆(一种库普弗细胞激活抑制剂,已知可预防APAP诱导的肝毒性)处理小鼠,可降低肝脏中观察到的病理生理反应,同时改变与APAP相关的NF-κB DNA结合活性变化。在对照肝脏中,NF-κB主要存在于实质细胞和内皮细胞中,主要由相对无活性的p50同型二聚体亚基组成。综上所述,这些研究表明肝毒性与特定转录因子的DNA结合活性的早期复杂变化有关。特别是,NF-κB和NF-IL6可能作为肝细胞衍生的炎症介质的负调节因子,这与先前在某些其他细胞系统如B淋巴细胞中观察到的情况类似。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验