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Microglia-neuronal signalling in neuropathic pain hypersensitivity 2.0.

机译:小胶质细胞神经元信号在神经性疼痛超敏反应2.0。

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摘要

Microglia are increasingly recognized as critical in the pathogenesis of pain hypersensitivity caused by injury to peripheral nerves. The core signalling pathway is through P2X4 purinergic receptors on the microglia which, via the release of brain-derived neurotrophic factor, cause disinhibition of nociceptive dorsal horn neurons by raising intracellular chloride levels. This disinhibition works in synergy with enhanced excitatory synaptic transmission in the dorsal horn to transform the output of the nociceptive network. There is increased discharge output, unmasking of responses to innocuous peripheral inputs and spontaneous activity in neurons that otherwise only signal nociception. Together the changes caused by microglia-neuron signalling may account for the main symptoms of neuropathic pain in humans.
机译:小胶质细胞日益被认为在由周围神经损伤引起的疼痛超敏反应的发病机理中至关重要。核心信号传导途径是通过小胶质细胞上的P2X4嘌呤能受体,通过释放脑源性神经营养因子,通过提高细胞内氯化物水平来抑制伤害性背角神经元。这种抑制作用与背角中兴奋性突触传递的增强协同作用,以改变伤害性网络的输出。放电输出增加,对无害的周围输入的反应和神经元中的自发活动的响应被掩盖,否则仅表示伤害感受。小胶质细胞-神经元信号转导引起的变化一起可能解释了人类神经性疼痛的主要症状。

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