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首页> 外文期刊>Neurochemical Research >Activation of NMDA Receptor is Associated with Up-regulation of COX-2 Expression in the Spinal Dorsal Horn during Nociceptive Inputs in Rats
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Activation of NMDA Receptor is Associated with Up-regulation of COX-2 Expression in the Spinal Dorsal Horn during Nociceptive Inputs in Rats

机译:NMDA受体的激活与大鼠伤害性输入过程中脊髓背角COX-2表达的上调相关。

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Cyclooxygenases-2 (COX-2) in the spinal dorsal horn is up-regulated and plays an important role in pain and hyperalgesia induced by nociceptive stimulation. The mechanisms involved in the up-regulation of spinal COX-2 during nociceptive stimulation are yet not well understood. Because the important role of NMDA and its receptor in transmission of nociceptive information in the spinal cord, activation of the spinal NMDA receptor might contribute to the up-regulation of spinal COX-2 expression. The present study was undertaken to demonstrate the above hypothesis by observing changes of COX-2 expression in the spinal dorsal horn in rats subjected to formalin test and intrathecal administration of NMDA, a selective NMDA receptor agonist, in conditions with or without presence of MK-801, an antagonist of NMDA receptor, using methods of Western blotting, reverse transcription polymerase chain reaction and immunohistochemistry. The results showed that intrathecal injection of MK-801, a noncompetitive antagonist of NMDA receptor, significantly suppressed the up-regulation of the COX-2 expression and characteristic pain behavior responses evoked in formalin test. Whereas, intrathecal injection of NMDA significantly up-regulated the expression of COX-2 in the spinal dorsal horn in a time course corresponding to that of nociceptive behavioral responses elicited by the intrathecal NMDA administration. In addition, the up-regulation of the COX-2 expression induced by the intrathecal NMDA was dose-dependent and blocked by prior administration of MK-801. These findings proved that activation of NMDA receptor is associated with the up-regulation of COX-2 expression in the spinal dorsal horn during nociceptive stimulation in rats.
机译:脊髓背角中的环氧合酶2(COX-2)上调,在伤害感受刺激引起的疼痛和痛觉过敏中起重要作用。伤害性刺激过程中参与脊髓COX-2上调的机制尚不十分清楚。由于NMDA及其受体在伤害感受信息在脊髓中的传递中起着重要作用,因此脊髓NMDA受体的活化可能有助于脊髓COX-2表达的上调。本研究通过观察福尔马林试验和鞘内施用NMDA(选择性NMDA受体激动剂)在有或没有MK-的条件下大鼠脊髓背角中COX-2表达的变化来证明上述假设。 801是NMDA受体的拮抗剂,使用蛋白质印迹,逆转录聚合酶链反应和免疫组化方法。结果表明,鞘内注射NMDA受体的非竞争性拮抗剂MK-801显着抑制了福尔马林测试中COX-2表达的上调和特征性疼痛行为反应。然而,鞘内注射NMDA在与鞘内NMDA施用引起的伤害性行为反应相对应的时间过程中显着上调了脊髓背角中COX-2的表达。另外,鞘内NMDA诱导的COX-2表达的上调是剂量依赖性的,并通过事先给予MK-801来阻断。这些发现证明,在大鼠伤害感受刺激过程中,NMDA受体的激活与脊髓背角中COX-2表达的上调有关。

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