首页> 外文期刊>British Journal of Pharmacology >Inhibition by nitric oxide-releasing compounds of prostacyclin production in human endothelial cells
【24h】

Inhibition by nitric oxide-releasing compounds of prostacyclin production in human endothelial cells

机译:一氧化氮释放化合物对人内皮细胞中前列环素产生的抑制作用

获取原文
获取原文并翻译 | 示例
       

摘要

The effects of two chemically unrelated nitric oxide(NO)-releasing compounds were studied on prostacyclin production in lipopolysaccharide (LPS)-stimulated human umbilical vein endothelial cells (HUVECs). The cells expressed cyclooxygenase-2(COX-2) protein and produced prostacyclin by NS- 398-sensitivve manner suggesting that prostacyclin production derives principally by COX-2 pathway. A novel NO-releasing oxatriazole derivative GEA 3175(1-30 μM) inhibited LPS-induced production Of prostacyclin in HUVECs in a dose-dependent manner being more potent than the earlier known NO- Donor S-nitroso-N-acetylpenicillamine(SNAP).
机译:研究了两种化学无关的一氧化氮释放化合物对脂多糖(LPS)刺激的人脐静脉内皮细胞(HUVEC)中前列环素产生的影响。细胞表达环加氧酶-2(COX-2)蛋白并通过NS-398敏感性方式产生前列环素,提示前列环素的产生主要来自COX-2途径。一种新型的释放NO的三唑衍生物GEA 3175(1-30μM)以剂量依赖的方式抑制LPS诱导的HUVEC中前列环素的产生,其作用比早期已知的NO-供体S-亚硝基-N-乙酰青霉胺(SNAP)更有效。

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