Niederberger Ellen, Kühlein Hilmar, Geisslinger Gerd
Pharmazentrum Frankfurt/ZAFES, Institut für Klinische Pharmakologie, Klinikum der Johann Wolfgang Goethe-Universität Frankfurt, Theodor Stern Kai 7, 60590 Frankfurt am Main, Germany.
Expert Rev Proteomics. 2008 Dec;5(6):799-818. doi: 10.1586/14789450.5.6.799.
Nerve injury or dysfunction in the peripheral and central nervous systems are the leading causes for the development of neuropathies, which are frequently associated with allodynia and hyperalgesia. Treatment of these disorders is often unsatisfactory due to side effects or insufficient analgesia of the currently available drugs. Therefore, elucidating the molecular mechanisms of neuropathic pain is an important prerequisite for the rational development of novel analgesic drugs for the therapy of neuropathic pain. Several proteomic approaches have been performed to explore protein modifications in the nervous system associated with neuropathies in different animal models, which might contribute to the detection of new drug targets. Furthermore, there are proteomic studies investigating human cerebrospinal fluid from patients suffering from neuropathies. The results of these studies and the potential clinical value of the proteomic data are summarized and discussed in this review.
外周和中枢神经系统的神经损伤或功能障碍是神经病变发展的主要原因,神经病变常与异常性疼痛和痛觉过敏相关。由于现有药物的副作用或镇痛效果不足,这些疾病的治疗往往不尽人意。因此,阐明神经性疼痛的分子机制是合理开发用于治疗神经性疼痛的新型镇痛药的重要前提。已经采用了几种蛋白质组学方法来探索不同动物模型中与神经病变相关的神经系统中的蛋白质修饰,这可能有助于发现新的药物靶点。此外,还有蛋白质组学研究调查了患有神经病变的患者的脑脊液。本文综述并讨论了这些研究的结果以及蛋白质组学数据的潜在临床价值。