Laboratorio de Neurobiología, Facultad de Química y Biología, Universidad de Santiago de Chile, Santiago 9170022, Chile.
Center for the Development of Nanoscience and Nanotechnology (CEDENNA), Santiago 9170022, Chile.
Int J Mol Sci. 2022 Jun 16;23(12):6705. doi: 10.3390/ijms23126705.
Pannexin 1 (Panx1) is involved in the spinal central sensitization process in rats with neuropathic pain, but its interaction with well-known, pain-related, ligand-dependent receptors, such as NMDA receptors (NMDAR) and P2X7 purinoceptors (P2X7R), remains largely unexplored. Here, we studied whether NMDAR- and P2X7R-dependent nociceptive signaling in neuropathic rats require the activation of Panx1 channels to generate spinal central sensitization, as assessed by behavioral (mechanical hyperalgesia) and electrophysiological (C-reflex wind-up potentiation) indexes. Administration of either a selective NMDAR agonist i.t. (NMDA, 2 mM) or a P2X7R agonist (BzATP, 150 μM) significantly increased both the mechanical hyperalgesia and the C-reflex wind-up potentiation, effects that were rapidly reversed (minutes) by i.t. administration of a selective pannexin 1 antagonist (10panx peptide, 300 μM), with the scores even reaching values of rats without neuropathy. Accordingly, 300 μM 10panx completely prevented the effects of NMDA and BzATP administered 1 h later, on mechanical hyperalgesia and C-reflex wind-up potentiation. Confocal immunofluorescence imaging revealed coexpression of Panx1 with NeuN protein in intrinsic dorsal horn neurons of neuropathic rats. The results indicate that both NMDAR- and P2X7R-mediated increases in mechanical hyperalgesia and C-reflex wind-up potentiation require neuronal Panx1 channel activation to initiate and maintain nociceptive signaling in neuropathic rats.
缝隙连接蛋白 1(Panx1)参与神经病理性疼痛大鼠的脊髓中枢敏化过程,但它与众所周知的、与疼痛相关的配体依赖性受体(如 NMDA 受体(NMDAR)和 P2X7 嘌呤能受体(P2X7R))的相互作用在很大程度上仍未得到探索。在这里,我们研究了神经病理性大鼠中 NMDAR 和 P2X7R 依赖性伤害性信号是否需要 Panx1 通道的激活来产生脊髓中枢敏化,这通过行为(机械性痛觉过敏)和电生理(C-反射波增强)指标来评估。鞘内给予选择性 NMDAR 激动剂(NMDA,2 mM)或 P2X7R 激动剂(BzATP,150 μM)均显著增加机械性痛觉过敏和 C-反射波增强,这些作用可通过鞘内给予选择性 Panx1 拮抗剂(10panx 肽,300 μM)迅速逆转(数分钟),评分甚至达到无神经病变大鼠的水平。因此,300 μM 10panx 完全阻止了 1 小时后给予 NMDA 和 BzATP 对机械性痛觉过敏和 C-反射波增强的作用。共聚焦免疫荧光成像显示 Panx1 与神经原特异性核蛋白(NeuN)蛋白在神经病理性大鼠背角固有神经元中存在共表达。结果表明,NMDAR 和 P2X7R 介导的机械性痛觉过敏和 C-反射波增强增加均需要神经元 Panx1 通道激活来启动和维持神经病理性大鼠的伤害性信号。