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神经病理性疼痛中的小胶质细胞:细胞和分子机制及治疗潜力。

Microglia in neuropathic pain: cellular and molecular mechanisms and therapeutic potential.

机构信息

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

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

出版信息

Nat Rev Neurosci. 2018 Mar;19(3):138-152. doi: 10.1038/nrn.2018.2. Epub 2018 Feb 8.

Abstract

Acute nociceptive pain is a key defence system that enables the detection of danger signals that threaten homeostasis and survival. However, chronic pain (such as the neuropathic pain that occurs after peripheral nerve injury) is not simply a consequence of the continuity of acute nociceptive signals but rather of maladaptive nervous system function. Over recent decades, studies have provided evidence for the necessity and sufficiency of microglia for the alterations in synaptic remodelling, connectivity and network function that underlie chronic pain and have shed light on the underlying molecular and cellular mechanisms. It is also becoming clear that microglia have active roles in brain regions important for the emotional and memory-related aspects of chronic pain. Recent advances in the development of new drugs targeting microglia and the establishment of new sources of human microglia-like cells may facilitate translation of these findings from bench to bedside.

摘要

急性伤害性疼痛是一种关键的防御系统,能够检测到威胁内稳态和生存的危险信号。然而,慢性疼痛(如外周神经损伤后发生的神经性疼痛)不仅仅是急性伤害性信号持续存在的结果,而是神经系统功能失调的结果。近几十年来,研究为小胶质细胞在突触重塑、连接和网络功能改变中所必需和充分的证据提供了依据,这些改变是慢性疼痛的基础,并揭示了潜在的分子和细胞机制。小胶质细胞在与慢性疼痛的情绪和记忆相关方面有关的大脑区域中发挥积极作用,这一点也越来越清楚。针对小胶质细胞的新药开发和新的人类小胶质样细胞来源的建立方面的最新进展,可能有助于将这些发现从实验室转化到临床。

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