The Role of Neuroglial Crosstalk and Synaptic Plasticity-Mediated Central Sensitization in Acupuncture Analgesia.

IF 3.1 4区 医学 Q2 Medicine Neural Plasticity Pub Date : 2021-01-18 eCollection Date: 2021-01-01 DOI:10.1155/2021/8881557
Zhongxi Lyu, Yongming Guo, Yinan Gong, Wen Fan, Baomin Dou, Ningcen Li, Shenjun Wang, Yuan Xu, Yangyang Liu, Bo Chen, Yi Guo, Zhifang Xu, Xiaowei Lin
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Abstract

Although pain is regarded as a global public health priority, analgesic therapy remains a significant challenge. Pain is a hypersensitivity state caused by peripheral and central sensitization, with the latter considered the culprit for chronic pain. This study summarizes the pathogenesis of central sensitization from the perspective of neuroglial crosstalk and synaptic plasticity and underlines the related analgesic mechanisms of acupuncture. Central sensitization is modulated by the neurotransmitters and neuropeptides involved in the ascending excitatory pathway and the descending pain modulatory system. Acupuncture analgesia is associated with downregulating glutamate in the ascending excitatory pathway and upregulating opioids, 𝛾-aminobutyric acid, norepinephrine, and 5-hydroxytryptamine in the descending pain modulatory system. Furthermore, it is increasingly appreciated that neurotransmitters, cytokines, and chemokines are implicated in neuroglial crosstalk and associated plasticity, thus contributing to central sensitization. Acupuncture produces its analgesic action by inhibiting cytokines, such as interleukin-1β, interleukin-6, and tumor necrosis factor-α, and upregulating interleukin-10, as well as modulating chemokines and their receptors such as CX3CL1/CX3CR1, CXCL12/CXCR4, CCL2/CCR2, and CXCL1/CXCR2. These factors are regulated by acupuncture through the activation of multiple signaling pathways, including mitogen-activated protein kinase signaling (e.g., the p38, extracellular signal-regulated kinases, and c-Jun-N-terminal kinase pathways), which contribute to the activation of nociceptive neurons. However, the responses of chemokines to acupuncture vary among the types of pain models, acupuncture methods, and stimulation parameters. Thus, the exact mechanisms require future clarification. Taken together, inhibition of central sensitization modulated by neuroglial plasticity is central in acupuncture analgesia, providing a novel insight for the clinical application of acupuncture analgesia.

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神经胶质细胞串联和突触可塑性介导的中枢敏化在针刺镇痛中的作用
尽管疼痛被视为全球公共卫生的优先事项,但镇痛治疗仍是一项重大挑战。疼痛是一种由外周和中枢敏化引起的超敏状态,后者被认为是慢性疼痛的罪魁祸首。本研究从神经胶质细胞串联和突触可塑性的角度总结了中枢敏化的发病机制,并强调了针灸的相关镇痛机制。中枢敏化受神经递质和神经肽的调节,它们参与了升序兴奋通路和降序疼痛调节系统。针刺镇痛与下调上升兴奋通路中的谷氨酸和上调下降疼痛调节系统中的类阿片、𝛾-氨基丁酸、去甲肾上腺素和 5-羟色胺有关。此外,人们越来越认识到,神经递质、细胞因子和趋化因子与神经胶质细胞的串联和相关可塑性有关,因此有助于中枢敏化。针灸通过抑制白细胞介素-1β、白细胞介素-6 和肿瘤坏死因子-α 等细胞因子,上调白细胞介素-10,以及调节趋化因子及其受体,如 CX3CL1/CX3CR1、CXCL12/CXCR4、CCL2/CCR2 和 CXCL1/CXCR2,产生镇痛作用。这些因子通过激活多种信号通路,包括丝裂原活化蛋白激酶信号通路(如p38、细胞外信号调节激酶和c-Jun-N-末端激酶通路)受针刺调节,从而促进痛觉神经元的激活。然而,趋化因子对针灸的反应因疼痛模型类型、针灸方法和刺激参数而异。因此,确切的机制还需要进一步明确。综上所述,神经胶质细胞可塑性对中枢敏化的抑制是针刺镇痛的核心,为针刺镇痛的临床应用提供了新的见解。
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来源期刊
Neural Plasticity
Neural Plasticity Neuroscience-Neurology
CiteScore
5.70
自引率
0.00%
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0
审稿时长
1 months
期刊介绍: Neural Plasticity is an international, interdisciplinary journal dedicated to the publication of articles related to all aspects of neural plasticity, with special emphasis on its functional significance as reflected in behavior and in psychopathology. Neural Plasticity publishes research and review articles from the entire range of relevant disciplines, including basic neuroscience, behavioral neuroscience, cognitive neuroscience, biological psychology, and biological psychiatry.
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