Departamento de Farmacobiología, Cinvestav, Sede Sur, Calzada de los Tenorios 235, Colonia Granjas Coapa, 14330 México, D.F., Mexico.
Neurosci Lett. 2011 Aug 21;501(1):4-9. doi: 10.1016/j.neulet.2011.06.048. Epub 2011 Jul 6.
This study assessed the role of the Na(+)/H(+) exchanger (NHE) in the formalin-induced nociception as well as the expression of the NHE isoform 1 (NHE1) in the rat spinal cord by using immunohistochemistry. Rats received a 50μl injection of diluted formalin (0.5%). Nociceptive behavior was quantified as the number of flinches of the injected paw. Intrathecal administration of the partially selective NHE1 inhibitors DMA, EIPA (0.3-30μM/rat) and the selective NHE1 inhibitor zoniporide (0.03-3μM/rat) significantly increased formalin-induced flinching behavior in a dose-dependent manner during both phases of the test. Immunohistochemical analysis of the rat lumbar spinal cord showed that NHE1 was mainly expressed in the lamina I of the dorsal horn of the spinal cord. Double immunofluorescence staining showed co-localization of NHE1 with the peptide-rich sensory nerve fiber markers, substance P and calcitonin gene-related peptide, but not with markers of neuronal cell bodies (NeuN), microglia (OX-42) or astroglia (GFAP). Collectively, these pharmacological and anatomical results suggest that spinal NHE1 plays a role in formalin-induced nociception acting as a protective protein extruding H(+).
本研究通过免疫组织化学方法评估了钠离子/氢离子交换器(NHE)在福尔马林诱导的疼痛中的作用,以及 NHE 同工型 1(NHE1)在大鼠脊髓中的表达。大鼠接受 50μl 稀释福尔马林(0.5%)注射。通过注射爪的抽搐次数来量化疼痛行为。鞘内给予部分选择性 NHE1 抑制剂 DMA、EIPA(0.3-30μM/大鼠)和选择性 NHE1 抑制剂 zoniporide(0.03-3μM/大鼠)可显著增加测试两个阶段福尔马林诱导的抽搐行为,呈剂量依赖性。对大鼠腰椎脊髓的免疫组织化学分析表明,NHE1 主要表达在脊髓背角的 I 层。双重免疫荧光染色显示 NHE1 与富含肽的感觉神经纤维标志物,P 物质和降钙素基因相关肽共定位,但与神经元细胞体标志物(NeuN)、小胶质细胞(OX-42)或星形胶质细胞(GFAP)不共定位。综上所述,这些药理学和解剖学结果表明,脊髓 NHE1 作为一种保护蛋白,在外排 H+方面在福尔马林诱导的疼痛中发挥作用。