...
首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >mu-Opioid receptor 6-transmembrane isoform: A potential therapeutic target for new effective opioids
【24h】

mu-Opioid receptor 6-transmembrane isoform: A potential therapeutic target for new effective opioids

机译:mu阿片受体6跨膜同工型:新有效阿片类药物的潜在治疗靶标

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The mu-opioid receptor (MOR) is the primary target for opioid analgesics. MOR induces analgesia through the inhibition of second messenger pathways and the modulation of ion channels activity. Nevertheless, cellular excitation has also been demonstrated, and proposed to mediate reduction of therapeutic efficacy and opioid-induced hyperalgesia upon prolonged exposure to opioids. In this mini-perspective, we review the recently identified, functional MOR isoform subclass, which consists of six transmembrane helices (6TM) and may play an important role in MOR signaling. There is evidence that 6TM MOR signals through very different cellular pathways and may mediate excitatory cellular effects rather than the classic inhibitory effects produced by the stimulation of the major (7TM) isoform. Therefore, the development of 6TM and 7TM MOR selective compounds represents a new and exciting opportunity to better understand the mechanisms of action and the pharmacodynamic properties of a new class of opioids. (C) 2014 Elsevier Inc. All rights reserved.
机译:mu阿片受体(MOR)是阿片类镇痛药的主要靶标。 MOR通过抑制第二信使途径和调节离子通道活性来诱导镇痛作用。然而,也已经证明了细胞兴奋,并提出在长时间暴露于阿片类药物时介导治疗功效的降低和阿片类药物引起的痛觉过敏。在此迷你视野中,我们回顾了最近鉴定的功能性MOR亚型亚型,该亚类由六个跨膜螺旋(6TM)组成,并可能在MOR信号传导中起重要作用。有证据表明6TM MOR通过非常不同的细胞途径发出信号,并且可能介导兴奋性细胞作用,而不是通过刺激主要(7TM)亚型产生的经典抑制作用。因此,开发6TM和7TM MOR选择性化合物代表了一个新的令人兴奋的机会,可以更好地了解新型阿片类药物的作用机理和药效学性质。 (C)2014 Elsevier Inc.保留所有权利。

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