...
首页> 外文期刊>International Journal of Molecular Sciences >Elevation of Inducible Nitric Oxide Synthase and Cyclooxygenase-2 Expression in the Mouse Brain after Chronic Nonylphenol Exposure
【24h】

Elevation of Inducible Nitric Oxide Synthase and Cyclooxygenase-2 Expression in the Mouse Brain after Chronic Nonylphenol Exposure

机译:慢性壬基酚暴露后小鼠脑中可诱导型一氧化氮合酶和环氧合酶-2表达的升高

获取原文

摘要

The present study was performed to investigate the effects of chronic administration of nonylphenol (NP) on the expression of inflammation-related genes in the brains of mice. NP was given orally by gavages at 0, 50, 100, and 200 mg/kg/d. The expression of inflammatory enzymes, inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), was evaluated by immunohistochemistry and immunoblotting assays. The nitric oxide (NO) level and nitric oxide synthase (NOS) activity were also measured by biochemical analyses. The results showed that NP at a high dose (200 mg/kg/d) significantly increased the expression of iNOS and COX-2 in both the hippocampus and cortex. In parallel with the increase in iNOS expression, the NO level was significantly greater at the dose of 200 mg/kg/d, compared to the control. The activity of NOS was also increased in the brain of mice at the dose of 100 and 200 mg/kg/d. These findings demonstrate that NP may have the potential to induce the chronic inflammation or cause neurotoxicity in the mouse brain.
机译:进行本研究以研究长期施用壬基酚(NP)对小鼠脑中炎症相关基因表达的影响。通过管饲法以0、50、100和200 mg / kg / d口服NP。通过免疫组织化学和免疫印迹分析评估炎症酶,诱导型一氧化氮合酶(iNOS)和环氧合酶2(COX-2)的表达。一氧化氮(NO)水平和一氧化氮合酶(NOS)活性也通过生化分析测量。结果表明,高剂量(200 mg / kg / d)的NP显着增加了海马和皮质中iNOS和COX-2的表达。与iNOS表达的增加同时,与对照组相比,在200 mg / kg / d的剂量下NO水平明显更高。以100和200 mg / kg / d的剂量,小鼠脑中NOS的活性也增加了。这些发现表明,NP可能具有诱发慢性炎症或引起小鼠脑神经毒性的潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号