首页> 外文期刊>Neuroreport >Activation of kappa opioid receptors in the rostral ventromedial medulla blocks stress-induced antinociception.
【24h】

Activation of kappa opioid receptors in the rostral ventromedial medulla blocks stress-induced antinociception.

机译:延髓腹侧延髓中κ阿片受体的激活可阻断应激诱导的镇痛作用。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Prior work has shown that kappa opioids may attenuate the effects of analgesic mu receptor agonists in some neural circuits related to pain modulation. This study examined whether hypoalgesia following exposure to a signal for shock is attenuated by infusions of the kappa agonist U69593 into the rostral ventromedial medulla (RVM). Rats were trained with paired or unpaired presentations of white noise and foot shock. On test days, tail flick latencies were measured before, during, and after exposure to the auditory conditioned stimulus (CS). One of three doses of U69593 (0.0445, 0.178 and 1.00 microg) or an equivalent volume of saline was injected into the RVM. Rats that had received noise-shock pairings displayed conditional hypoalgesia (CHA) compared to those given unpaired presentations. Expression of CHA was completely blocked by the highest dose of U69593 (1.00 microg) injected 20 min before testing, indicating an antagonistic effect of U69593 on expression of CHA. These findings are discussed in terms of the evidence for antagonism of morphine- and DAMGO-induced hypoalgesia by kappa agonists.
机译:先前的研究表明,在某些与疼痛调节有关的神经回路中,κ阿片类药物可能会减弱镇痛性mu受体激动剂的作用。这项研究研究了将κ激动剂U69593输注到延髓腹侧延髓(RVM)后,是否会减弱电击信号后的痛觉过敏。用成对或不成对的白噪声和足部电击训练大鼠。在测试日,在暴露于听觉条件刺激(CS)之前,之中和之后测量甩尾潜伏期。将三剂U69593(0.0445、0.178和1.00微克)之一或等体积的盐水注入RVM。与未配对的老鼠相比,接受了噪音冲击配对的老鼠表现出条件性痛觉过敏(CHA)。测试前20分钟注射最高剂量的U69593(1.00微克)完全阻断了CHA的表达,表明U69593对CHA的表达具有拮抗作用。将根据κ激动剂对吗啡和DAMGO诱导的痛觉过敏的拮抗证据讨论这些发现。

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