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小胶质细胞与神经病理性疼痛。

Microglia in Neuropathic Pain.

机构信息

The Institute for Advanced Study, Kyushu University, Fukuoka, Japan.

出版信息

Adv Neurobiol. 2024;37:399-403. doi: 10.1007/978-3-031-55529-9_22.

Abstract

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 (E) 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.

摘要

神经病理性疼痛(NP)是由躯体感觉系统的损伤或疾病引起的疼痛。NP 的一个主要特征是触觉过敏(对通常无害的刺激产生疼痛反应)。2003 年,提出了一种突破性的诱导 NP 的策略,即外周神经损伤(PNI)后,脊髓背角(SDH)的小胶质细胞被激活,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,小胶质细胞 P2X4R 的刺激会引发脑源性神经营养因子(BDNF)的释放,导致二级感觉神经元的阴离子反转电位(E)去极化。这些发现和其他事实表明了无害触摸刺激引起严重疼痛的机制,以及小胶质细胞在该机制中的重要作用。

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