Department of Oral Diagnosis, School of Dentistry, Nihon University, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan.
Brain Res. 2010 Nov 4;1359:81-9. doi: 10.1016/j.brainres.2010.08.073. Epub 2010 Aug 31.
The kappa-opioid receptor (KOR) antagonist norbinaltorphimine (nor-BNI) attenuates behavioral antinociception produced by spinal administration of the cannabinoid receptor agonist delta-9-tetrahydorcannabinol (THC). The present study examined the ability of nor-BNI to prevent cannabinoid-induced inhibition of medullary dorsal horn (MDH) nociceptive neurons and antinociception produced by the cannabinoid agonist WIN 55,212-2 (WIN-2). Extracellular, single-unit recordings of lamina I and lamina V MDH neurons were performed in urethane anesthetized rats. Heat-evoked activity was measured before and after local brainstem application of nor-BNI or vehicle followed by WIN-2. In both lamina I and lamina V neurons, prior application of nor-BNI prevented the inhibition of heat-evoked activity by WIN-2. In separate experiments, the contribution of KOR to cannabinoid-induced increases in heat-evoked head withdrawal latencies was assessed in lightly urethane-anesthetized rats. Antinociception produced by intrathecal administration of WIN-2 and THC was attenuated by prior administration of nor-BNI. In contrast, antinociception produced by the cannabinoid CP55940 remained unaffected by prior administration of nor-BNI. These results indicate that cannabinoid inhibition of nociceptive reflexes produced by WIN-2 and THC may result from inhibition of dorsal horn neurons through a KOR-dependent mechanism.
κ 阿片受体(KOR)拮抗剂诺比那嗪(nor-BNI)可减弱脊髓给予大麻素受体激动剂 delta-9-四氢大麻醇(THC)产生的行为性抗伤害作用。本研究检测了 nor-BNI 预防大麻素诱导的背角(MDH)伤害性神经元抑制和大麻素激动剂 WIN 55,212-2(WIN-2)产生的抗伤害作用的能力。在乌拉坦麻醉的大鼠中进行了脊髓背角 I 层和 V 层的细胞外单位记录。在局部脑桥应用 nor-BNI 或载体后,测量热诱发活动在之前和之后的变化,随后给予 WIN-2。在 I 层和 V 层神经元中,nor-BNI 的预先应用可预防 WIN-2 对热诱发活动的抑制。在单独的实验中,在轻度乌拉坦麻醉的大鼠中评估了 KOR 对大麻素诱导的热诱发头部退缩潜伏期增加的贡献。鞘内给予 WIN-2 和 THC 产生的抗伤害作用被 nor-BNI 的预先给予所减弱。相比之下,nor-BNI 的预先给予对 CP55940 产生的大麻素的抗伤害作用没有影响。这些结果表明,WIN-2 和 THC 抑制伤害性反射可能是通过 KOR 依赖性机制抑制背角神经元而产生的。