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小胶质细胞与难治性慢性疼痛。

Microglia and intractable chronic pain.

机构信息

Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Glia. 2013 Jan;61(1):55-61. doi: 10.1002/glia.22379. Epub 2012 Jun 27.

Abstract

Many pathological processes within the central nervous system are mediated by complex interactions between neurons and resident glial cells. In the case of painful peripheral neuropathy, spinal microglia react and undergo a series of changes that directly influence the establishment of neuropathic pain states. Purinergic signaling has been shown to be at the center of this reactivity, and here we review recent mechanistic advances describing the importance of microglial P2 receptors and their interactions with neuronal populations in the development of neuropathic pain.

摘要

中枢神经系统内的许多病理过程都是由神经元和固有神经胶质细胞之间的复杂相互作用介导的。在痛性周围神经病变的情况下,脊髓小胶质细胞会发生反应并经历一系列变化,这些变化直接影响到神经病理性疼痛状态的建立。嘌呤能信号转导被证明处于这种反应的中心,在这里我们回顾了最近描述小胶质细胞 P2 受体的重要性及其与神经元群体相互作用在神经病理性疼痛发展中的机制进展。

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