Kunz Susanne, Tegeder Irmgard, Coste Ovidiu, Marian Claudiu, Pfenninger Anja, Corvey Carsten, Karas Michael, Geisslinger Gerd, Niederberger Ellen
pharmazentrum frankfurt/ZAFES, Klinikum der Johann Wolfgang Goethe-Universität Theodor Stern Kai 7, 60590 Frankfurt am Main, Germany.
Neurosci Lett. 2005 Jun 24;381(3):289-93. doi: 10.1016/j.neulet.2005.02.022.
Pathological pain associated either with peripheral tissue damage and inflammation (inflammatory pain) or peripheral nerve injury (neuropathic pain) is characterized by persistent pain hypersensitivity. This hypersensitivity is believed to be mediated by sensitization of nociceptors and spinal dorsal horn neurons leading to hyperalgesia and allodynia. Changes of protein expression and/or phosphorylation are known to contribute to the development of this hyperexcitability of the nociceptive system. In the present study we analyzed protein patterns in the spinal cord following paw inflammation or sciatic nerve injury using two-dimensional (2D) gel electrophoresis combined with MALDI-TOF mass spectrometry. 2D-PAGE revealed nine and five regulated proteins following paw inflammation and sciatic nerve damage, respectively. These regulated proteins had not been identified previously with other methods. There was no overlap of regulated proteins between models except for the small heat shock protein alpha-crystallin, which was decreased in both models. In conclusion, this study illustrates that employment of the proteomic 2D-PAGE approach allows for identification of novel regulated proteins that may be involved in the central sensitization and possibly manifestation of chronic pain.
与外周组织损伤和炎症相关的病理性疼痛(炎性疼痛)或外周神经损伤(神经性疼痛)的特征是持续性疼痛超敏反应。这种超敏反应被认为是由伤害感受器和脊髓背角神经元的敏化介导的,导致痛觉过敏和异常性疼痛。已知蛋白质表达和/或磷酸化的变化有助于伤害感受系统这种过度兴奋性的发展。在本研究中,我们使用二维(2D)凝胶电泳结合基质辅助激光解吸电离飞行时间质谱法分析了爪部炎症或坐骨神经损伤后脊髓中的蛋白质模式。二维聚丙烯酰胺凝胶电泳分别在爪部炎症和坐骨神经损伤后揭示了9种和5种调节蛋白。这些调节蛋白以前未用其他方法鉴定过。除了小热休克蛋白α-晶状体蛋白在两种模型中均减少外,模型之间调节蛋白没有重叠。总之,本研究表明蛋白质组二维聚丙烯酰胺凝胶电泳方法的应用能够鉴定可能参与中枢敏化以及慢性疼痛可能表现的新型调节蛋白。