首页> 美国卫生研究院文献>Mediators of Inflammation >Cyclic-AMP mediated drugs: differential or global reduction of eicosanoid synthesis in the isolated rat lung?
【2h】

Cyclic-AMP mediated drugs: differential or global reduction of eicosanoid synthesis in the isolated rat lung?

机译:环-AMP介导的药物:分离的大鼠肺中类花生酸合成的差异或整体减少?

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In this study the question was addressed whether cAMP mediated drugs induce a differential reduction of branches of the arachidonic acid metabolism rather than a global reduction of eicosanoid synthesis. The isolated lungs of actively sensitized rats were employed to study prostaglandin and leukotriene release in the presence and absence of the cAMP mediated drugs theophylline, milrinone, sulmazole, isobutyl-methylxanthine and salbutamol. The release of eicosanoids as measured by RIA was predominantly basal and continuous, with a mild antigen induced stimulation only for TXB2 and the leukotrienes. All drugs reduced eicosanoid release globally. It is concluded that cAMP mediated drugs interfere with arachidonic acid metabolism at a site proximal to the branching into lipoxygenase and cyclo-oxygenase pathways.
机译:在这项研究中,该问题得到解决,即cAMP介导的药物是否诱导花生四烯酸代谢的分支差异减少而不是类花生酸合成的整体减少。在存在和不存在cAMP介导的药物茶碱,米力农,舒马唑,异丁基甲基黄嘌呤和沙丁胺醇的情况下,采用主动敏化大鼠的肺进行研究前列腺素和白三烯的释放。通过RIA测定的类花生酸的释放主要是基础和连续的,仅对TXB2和白三烯具有温和的抗原诱导刺激作用。所有药物均可降低全球类花生酸的释放。结论是,cAMP介导的药物在分支到脂加氧酶和环加氧酶途径附近的位置干扰了花生四烯酸的代谢。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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