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神经变性后神经性疼痛中嘌呤能信号介导的神经元-小胶质细胞相互作用。

Neuron-microglia interaction by purinergic signaling in neuropathic pain following neurodegeneration.

作者信息

Tsuda Makoto, Inoue Kazuhide

机构信息

Department of Life Innovation, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Neuropharmacology. 2016 May;104:76-81. doi: 10.1016/j.neuropharm.2015.08.042. Epub 2015 Aug 29.

Abstract

Neuropathic pain, a chronic pain condition following nerve damage and degeneration, involves aberrant excitability in the dorsal horn of the spinal cord. A growing body of evidence has shown that the aberrant excitability might not be a consequence merely of changes in neurons, but rather of multiple alterations in glial cells, such as microglia, the immune cells of the central nervous system. Extracellular nucleotides play an important role in neuron-microglia communication through purinergic P2X and P2Y receptors expressed in microglia. Importantly, inhibiting the function or expression of these microglial molecules suppresses aberrant excitability of dorsal horn neurons and neuropathic pain, suggesting a crucial role for microglial purinergic signaling in mechanisms of neuropathic pain. Here, we describe recent advances in the understanding of neuron-microglia interactions by purinergic signaling in neuropathic pain following neurodegeneration. This article is part of the Special Issue entitled 'Purines in Neurodegeneration and Neuroregeneration'.

摘要

神经性疼痛是一种神经损伤和退变后的慢性疼痛状态,涉及脊髓背角的异常兴奋性。越来越多的证据表明,这种异常兴奋性可能不仅仅是神经元变化的结果,而是胶质细胞(如小胶质细胞,中枢神经系统的免疫细胞)多种改变的结果。细胞外核苷酸通过小胶质细胞中表达的嘌呤能P2X和P2Y受体在神经元-小胶质细胞通讯中发挥重要作用。重要的是,抑制这些小胶质细胞分子的功能或表达可抑制背角神经元的异常兴奋性和神经性疼痛,这表明小胶质细胞嘌呤能信号在神经性疼痛机制中起关键作用。在此,我们描述了在神经退变后神经性疼痛中,通过嘌呤能信号理解神经元-小胶质细胞相互作用的最新进展。本文是名为“神经退变和神经再生中的嘌呤”特刊的一部分。

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