Boucher T J, Okuse K, Bennett D L, Munson J B, Wood J N, McMahon S B
Centre for Neuroscience Research, King's College London, London SE1 7EH, UK.
Science. 2000 Oct 6;290(5489):124-7. doi: 10.1126/science.290.5489.124.
Neuropathic pain arises as a debilitating consequence of nerve injury. The etiology of such pain is poorly understood, and existing treatment is largely ineffective. We demonstrate here that glial cell line-derived neurotrophic factor (GDNF) both prevented and reversed sensory abnormalities that developed in neuropathic pain models, without affecting pain-related behavior in normal animals. GDNF reduces ectopic discharges within sensory neurons after nerve injury. This may arise as a consequence of the reversal by GDNF of the injury-induced plasticity of several sodium channel subunits. Together these findings provide a rational basis for the use of GDNF as a therapeutic treatment for neuropathic pain states.
神经性疼痛是神经损伤导致的一种使人衰弱的后果。这种疼痛的病因尚不清楚,现有的治疗方法大多无效。我们在此证明,胶质细胞系源性神经营养因子(GDNF)既能预防又能逆转神经性疼痛模型中出现的感觉异常,同时不影响正常动物的疼痛相关行为。GDNF可减少神经损伤后感觉神经元内的异位放电。这可能是由于GDNF逆转了损伤诱导的几种钠通道亚基的可塑性所致。这些发现共同为将GDNF用作神经性疼痛状态的治疗方法提供了合理依据。