P2X7受体介导性IL-18/IL-18R信号转导在吗啡耐受中的作用:大鼠脊髓中的多重胶质细胞-神经元联系

Role of P2X7 receptor-mediated IL-18/IL-18R signaling in morphine tolerance: Multiple glial-neuronal dialogues in the rat spinal cord
2012-10-11 15:23点击:98次发表评论
作者:Chen, M.-L., Cao, H., Chu, Y.-X., Cheng, L.-Z., Li
机构: 复旦大学医学神经生物学国家重点实验室
期刊: J Pain2012年10月10期13卷

Zhao, Z.-Q.; Institute of Neurobiology, State Key Laboratory of Medical Neurobiology, Fudan University, 138 Yi Xue-Yuan Road, Shanghai 200032, China; email:zqzhao@fudan.edu.cn

The glial function in morphine tolerance has been explored, but its mechanisms remain unclear. Our previous study has showed that microglia-expressed P2X7 receptors (P2X7R) contribute to the induction of tolerance to morphine analgesia in rats. This study further explored the potential downstream mechanisms of P2X7R underlying morphine tolerance. The results revealed that the blockade of P2X7 receptor by P2X7R antagonist or targeting small interfering RNA (siRNA) reduced tolerance to morphine analgesia in the pain behavioral test and spinal extracellular recordings in vivo and whole-cell recording of the spinal cord slice in vitro. Chronic morphine treatment induced an increase in the expression of interleukin (IL)-18 by microglia, IL-18 receptor (IL-18R) by astrocytes, and protein kinase Cγ (PKCγ) by neurons in the spinal dorsal horn, respectively, which was blocked by a P2X7R antagonist or targeting siRNA. Chronic morphine treatment also induced an increased release of D-serine from the spinal astrocytes. Further, both D-amino acid oxygenase (DAAO), a degrading enzyme of D-serine, and bisindolylmaleimide α (BIM), a PKC inhibitor, attenuated morphine tolerance. The present study demonstrated a spinal mechanism underlying morphine tolerance, in which chronic morphine triggered multiple dialogues between glial and neuronal cells in the spinal cord via a cascade involving a P2X7R-IL-18-D-serine-N-methyl-D-aspartate receptor (NMDAR)-PKCγ-mediated signaling pathway. Perspective: The present study shows that glia-neuron interaction via a cascade (P2X7R-IL-18-D-serine-NMDAR-PKCγ) in the spinal cord plays an important role in morphine tolerance. This article may represent potential new therapeutic targets for preventing morphine analgesic tolerance in clinical management of chronic pain. © 2012 by the American Pain Society.

Institute of Neurobiology, State Key Laboratory of Medical Neurobiology, Fudan University, 138 Yi Xue-Yuan Road, Shanghai 200032, China

通讯作者:Zhao, Z.-Q.; Institute of Neurobiology, State Key Laboratory of Medical Neurobiology, Fudan University, 138 Yi Xue-Yuan Road, Shanghai 200032, China; email:zqzhao@fudan.edu.cn
学科代码:神经病学   关键词:P2X7受体介导性IL-18/IL-18R信号转导在吗啡耐受
来源: Scopus
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