Suppr超能文献

孤啡肽对吗啡诱导镇痛的双向调节作用:在大鼠脑内起拮抗作用而在脊髓中起增强作用。

Bidirectional modulatory effect of orphanin FQ on morphine-induced analgesia: antagonism in brain and potentiation in spinal cord of the rat.

作者信息

Tian J H, Xu W, Fang Y, Mogil J S, Grisel J E, Grandy D K, Han J S

机构信息

Neuroscience Research Center, Beijing Medical University, China.

出版信息

Br J Pharmacol. 1997 Feb;120(4):676-80. doi: 10.1038/sj.bjp.0700942.

Abstract
  1. The present study was designed to investigate further the effects of the newly discovered orphanin FQ (OFQ)-the endogenous ligand for the orphan opioid receptor (called, e.g., ORL, and LC132)-on pain modulation in the rat. We used the tail-flick assay as a nociceptive index. 2. When injected into a cerebral ventricle, OFQ (4 fmol-10 nmol) has no effect on basal tail-flick latency by itself at any dose, but dose-dependently antagonizes systemic morphine analgesia (400 fmol 50 nmol). 3. Injected intrathecally, OFQ (3 and 10 nmol) displayed an analgesic effect without producing motor dysfunction, and potentiated morphine analgesia (1 and 10 nmol). 4. The anti-opioid effect of OFQ in rat brain and the high level of expression of LC132/ORL, receptor in the locus coeruleus indicated a possible role of OFQ in the precipitation of opiate withdrawal symptoms. However, no such precipitation was observed by OFQ in morphine-dependent rats.
摘要
  1. 本研究旨在进一步探究新发现的孤啡肽FQ(OFQ)——孤儿阿片受体(如ORL、LC132)的内源性配体——对大鼠疼痛调节的影响。我们采用甩尾试验作为伤害性指标。2. 当注入脑室时,OFQ(4飞摩尔至10纳摩尔)无论剂量如何,自身对基础甩尾潜伏期均无影响,但能剂量依赖性地拮抗全身吗啡镇痛作用(400飞摩尔至50纳摩尔)。3. 鞘内注射时,OFQ(3纳摩尔和10纳摩尔)显示出镇痛作用且未产生运动功能障碍,并增强了吗啡镇痛作用(1纳摩尔和10纳摩尔)。4. OFQ在大鼠脑内的抗阿片样作用以及蓝斑中LC132/ORL受体的高表达表明OFQ在阿片类药物戒断症状的诱发中可能起作用。然而,在吗啡依赖大鼠中未观察到OFQ诱发此类症状。

相似文献

引用本文的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验