神经病理性疼痛中的小胶质细胞

Q3 Neuroscience
Kazuhide Inoue
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引用次数: 0

摘要

神经性疼痛(NP)是躯体感觉系统病变或疾病引起的疼痛。NP 的一个主要特征是触觉过敏(对正常无害刺激的疼痛反应)。2003 年,有人提出了一种诱导 NP 的突破性策略,即在周围神经损伤(PNI)后激活脊髓背角(SDH)的小胶质细胞,使其过度表达 P2X4 受体(P2X4R),并在诱导触觉过敏中发挥重要作用。2005 年有报道称,刺激小胶质细胞的 P2X4Rs 会诱发脑源性神经营养因子(BDNF)的释放,从而导致次级感觉神经元的阴离子反转电位(Eanion)发生去极化转变。这些发现和其他事实表明了无害的触觉刺激导致剧烈疼痛的机制,以及小胶质细胞在该机制中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microglia in Neuropathic Pain.

Neuropathic pain (NP) is pain resulting from lesions or disease of the somatosensory system. A cardinal feature of NP is tactile allodynia (a painful response to normally innocuous stimulation). In 2003, a breakthrough strategy for inducing NP was proposed in which microglia of the spinal dorsal horn (SDH) are activated after peripheral nerve injury (PNI) to overexpress P2X4 receptor (P2X4R) and play an important role in inducing tactile allodynia. In 2005, it was reported that stimulation of microglial P2X4Rs evokes the release of brain-derived neurotrophic factor (BDNF), which causes a depolarizing shift of the anion reversal potential (Eanion) of secondary sensory neurons. These findings and other facts suggest the mechanism by which innocuous touch stimuli cause severe pain and the important role of microglia in the mechanism.

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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
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2.80
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