首页> 外文期刊>Trends in pharmacological sciences >The NMDA receptoritric oxide pathway: a target for the therapeutic and toxic effects of lithium.
【24h】

The NMDA receptoritric oxide pathway: a target for the therapeutic and toxic effects of lithium.

机译:NMDA受体/一氧化氮途径:锂的治疗和毒性作用的靶标。

获取原文
获取原文并翻译 | 示例
       

摘要

Although lithium has largely met its initial promise as the first drug discovered in the modern era of psychopharmacology, to date no definitive mechanism for its effects has been established. It has been proposed that lithium exerts its therapeutic effects by interfering with signal transduction through G-protein-coupled receptor (GPCR) pathways or direct inhibition of specific targets in signaling systems, including inositol monophosphatase and glycogen synthase kinase-3 (GSK-3). Recently, increasing evidence has suggested that N-methyl-D-aspartate receptor (NMDAR)itric oxide (NO) signaling could mediate some lithium-induced responses in the brain and peripheral tissues. However, the probable role of the NMDAR/NO system in the action of lithium has not been fully elucidated. In this review, we discuss biochemical, preclinical/behavioral and physiological evidence that implicates NMDAR/NO signaling in the therapeutic effect of lithium. NMDAR/NO signaling could also explain some of side effects of lithium.
机译:尽管锂已基本实现了其最初的承诺,成为现代心理药理学时代发现的第一种药物,但迄今为止,尚未建立确定其作用的确切机制。有人提出锂通过干扰G蛋白偶联受体(GPCR)途径的信号转导或直接抑制信号系统中特定靶标(包括肌醇单磷酸酶和糖原合酶激酶3(GSK-3))发挥其治疗作用。 。最近,越来越多的证据表明N-甲基-D-天门冬氨酸受体(NMDAR)/一氧化氮(NO)信号传导可以介导一些锂诱导的大脑和周围组织的反应。但是,尚未完全阐明NMDAR / NO系统在锂作用中的可能作用。在这篇综述中,我们讨论了生化,临床前/行为和生理学证据,这些证据牵涉NMDAR / NO信号传导锂的治疗作用。 NMDAR / NO信号也可以解释锂的一些副作用。

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