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小胶质细胞与持续性疼痛中的脊髓突触可塑性。

Microglia and spinal cord synaptic plasticity in persistent pain.

机构信息

Pain Signaling and Plasticity Laboratory, Department of Anesthesiology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Neural Plast. 2013;2013:753656. doi: 10.1155/2013/753656. Epub 2013 Aug 18.

Abstract

Microglia are regarded as macrophages in the central nervous system (CNS) and play an important role in neuroinflammation in the CNS. Microglial activation has been strongly implicated in neurodegeneration in the brain. Increasing evidence also suggests an important role of spinal cord microglia in the genesis of persistent pain, by releasing the proinflammatory cytokines tumor necrosis factor-alpha (TNFα), Interleukine-1beta (IL-1β), and brain derived neurotrophic factor (BDNF). In this review, we discuss the recent findings illustrating the importance of microglial mediators in regulating synaptic plasticity of the excitatory and inhibitory pain circuits in the spinal cord, leading to enhanced pain states. Insights into microglial-neuronal interactions in the spinal cord dorsal horn will not only further our understanding of neural plasticity but may also lead to novel therapeutics for chronic pain management.

摘要

小胶质细胞被认为是中枢神经系统(CNS)中的巨噬细胞,在 CNS 中的神经炎症中发挥重要作用。小胶质细胞的激活被强烈暗示与大脑中的神经退行性变有关。越来越多的证据还表明,脊髓小胶质细胞通过释放促炎细胞因子肿瘤坏死因子-α(TNFα)、白细胞介素-1β(IL-1β)和脑源性神经营养因子(BDNF),在持续性疼痛的产生中起着重要作用。在这篇综述中,我们讨论了最近的发现,这些发现说明了小胶质细胞介质在调节脊髓兴奋性和抑制性疼痛回路的突触可塑性方面的重要性,导致增强的疼痛状态。对脊髓背角中小胶质细胞-神经元相互作用的深入了解不仅将加深我们对神经可塑性的理解,还可能为慢性疼痛管理带来新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a92d/3759269/ad064bd04f34/NP2013-753656.001.jpg

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