Suter Marc R, Wen Yeong-Ray, Decosterd Isabelle, Ji Ru-Rong
Pain Research Center, Department of Anesthesiology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Neuron Glia Biol. 2007 Aug;3(3):255-68. doi: 10.1017/S1740925X08000100.
Management of chronic pain is a real challenge, and current treatments that focus on blocking neurotransmission in the pain pathway have resulted in limited success. Activation of glial cells has been widely implicated in neuroinflammation in the CNS, leading to neurodegeneration in conditions such as Alzheimer's disease and multiple sclerosis. The inflammatory mediators released by activated glial cells, such as tumor necrosis factor-a and interleukin-1b not only cause neurodegeneration in these disease conditions, but also cause abnormal pain by acting on spinal cord dorsal horn neurons in injury conditions. Pain can also be potentiated by growth factors such as brain-derived growth factor and basic fibroblast growth factor, which are produced by glia to protect neurons. Thus, glial cells can powerfully control pain when they are activated to produce various pain mediators. We review accumulating evidence that supports an important role for microglial cells in the spinal cord for pain control under injury conditions (e.g. nerve injury). We also discuss possible signaling mechanisms, in particular mitogen-activated protein kinase pathways that are crucial for glial-mediated control of pain.Investigating signaling mechanisms in microglia might lead to more effective management of devastating chronic pain.
慢性疼痛的管理是一项真正的挑战,目前专注于阻断疼痛通路中神经传递的治疗方法取得的成功有限。胶质细胞的激活在中枢神经系统的神经炎症中广泛涉及,导致在诸如阿尔茨海默病和多发性硬化症等病症中发生神经退行性变。激活的胶质细胞释放的炎症介质,如肿瘤坏死因子-α和白细胞介素-1β,不仅在这些疾病状态下导致神经退行性变,而且在损伤状态下通过作用于脊髓背角神经元引起异常疼痛。疼痛也可由胶质细胞产生的用于保护神经元的生长因子如脑源性神经营养因子和碱性成纤维细胞生长因子增强。因此,当胶质细胞被激活以产生各种疼痛介质时,它们可以有力地控制疼痛。我们综述了越来越多的证据,这些证据支持小胶质细胞在脊髓中对损伤状态(如神经损伤)下的疼痛控制起重要作用。我们还讨论了可能的信号传导机制,特别是有丝分裂原活化蛋白激酶途径,其对于胶质细胞介导的疼痛控制至关重要。研究小胶质细胞中的信号传导机制可能会导致对毁灭性慢性疼痛更有效的管理。