Suppr超能文献

小胶质细胞调控作为慢性疼痛治疗靶点:从基础到临床再到基础。

Microglial Modulation as a Target for Chronic Pain: From the Bench to the Bedside and Back.

机构信息

From the Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, Stanford, California.

University of Colorado School of Medicine, Denver, Colorado.

出版信息

Anesth Analg. 2019 Apr;128(4):737-746. doi: 10.1213/ANE.0000000000004033.

Abstract

With a widespread opioid epidemic and profound biopsychosocial implications, chronic pain is a multifaceted public health issue requiring urgent attention. The treatment of chronic pain is particularly important to anesthesiologists given our unique role as perioperative physicians and pain medicine specialists. The present review details the recent shift from a neuronal theory of chronic pain to one that includes complex neuron-glia interactions. In particular, we highlight microglia, the myeloid-lineage cells of the central nervous system, as initiators of a postinjury neuroimmune response that contributes to the acute to chronic pain transition. We discuss ever-advancing preclinical studies, wherein significant success has been made through pharmacologic and genetic modulation of microglia, and we emphasize where these approaches have made the transition to the clinical realm. Furthermore, we highlight the most current, novel efforts to visualize glial activation in vivo using positron emission tomography and improve the diagnosis of chronic pain through radiotracer binding of specific targets, like the 18 kDa translocator protein in microglia and myeloid-lineage cells. Our rapidly advancing knowledge about microglia and their involvement in pain suggests that the era of glial-targeted therapeutics is just beginning so long as we refocus our attention on optimizing preclinical studies using a clinically informed approach, before translation.

摘要

慢性疼痛是一个多方面的公共卫生问题,具有广泛的阿片类药物流行和深远的生物心理社会影响,需要紧急关注。鉴于我们作为围手术期医生和疼痛医学专家的独特角色,慢性疼痛的治疗对麻醉师尤为重要。本综述详细介绍了从慢性疼痛的神经元理论向包括复杂的神经元-胶质相互作用理论的转变。特别是,我们强调小胶质细胞,即中枢神经系统的髓系细胞,作为损伤后神经免疫反应的启动者,导致急性到慢性疼痛的转变。我们讨论了不断发展的临床前研究,其中通过小胶质细胞的药理学和遗传学调节取得了重大成功,并强调了这些方法在向临床领域过渡的情况。此外,我们还强调了使用正电子发射断层扫描术(PET)在体内可视化胶质细胞激活的最新、新颖的努力,并通过放射性示踪剂与特定靶点(如小胶质细胞和髓系细胞中的 18 kDa 转位蛋白)的结合来改善慢性疼痛的诊断。我们对小胶质细胞及其在疼痛中的作用的快速发展的认识表明,只要我们重新关注使用基于临床的方法优化临床前研究,在转化之前,靶向神经胶质的治疗时代才刚刚开始。

相似文献

1
Microglial Modulation as a Target for Chronic Pain: From the Bench to the Bedside and Back.
Anesth Analg. 2019 Apr;128(4):737-746. doi: 10.1213/ANE.0000000000004033.
2
Central Nervous System Targets: Glial Cell Mechanisms in Chronic Pain.
Neurotherapeutics. 2020 Jul;17(3):846-860. doi: 10.1007/s13311-020-00905-7.
4
Temporal Contribution of Myeloid-Lineage TLR4 to the Transition to Chronic Pain: A Focus on Sex Differences.
J Neurosci. 2021 May 12;41(19):4349-4365. doi: 10.1523/JNEUROSCI.1940-20.2021. Epub 2021 Apr 12.
6
The purinergic system and glial cells: emerging costars in nociception.
Biomed Res Int. 2014;2014:495789. doi: 10.1155/2014/495789. Epub 2014 Sep 3.
8
Microglia-Neuron Communication in Epilepsy.
Glia. 2017 Jan;65(1):5-18. doi: 10.1002/glia.23006. Epub 2016 May 18.
9
Neuroinflammation and Central Sensitization in Chronic and Widespread Pain.
Anesthesiology. 2018 Aug;129(2):343-366. doi: 10.1097/ALN.0000000000002130.
10
Unconventional Role of Caspase-6 in Spinal Microglia Activation and Chronic Pain.
Mediators Inflamm. 2017;2017:9383184. doi: 10.1155/2017/9383184. Epub 2017 Feb 7.

引用本文的文献

2
Lighting the shades of hidden pain: a role for spinal cord neurons and microglia in vestibulodynia.
Neural Regen Res. 2025 Oct 1;20(10):2898-2900. doi: 10.4103/NRR.NRR-D-24-00673. Epub 2024 Sep 24.
3
5
Effective Doses of Low-Dose Naltrexone for Chronic Pain - An Observational Study.
J Pain Res. 2024 Mar 21;17:1273-1284. doi: 10.2147/JPR.S451183. eCollection 2024.
7
Repopulated spinal cord microglia exhibit a unique transcriptome and contribute to pain resolution.
Cell Rep. 2024 Feb 27;43(2):113683. doi: 10.1016/j.celrep.2024.113683. Epub 2024 Jan 22.
9
The Relationship Between Chronic Pain and Cognitive Impairment in the Elderly: A Review of Current Evidence.
J Pain Res. 2023 Jul 7;16:2309-2319. doi: 10.2147/JPR.S416253. eCollection 2023.

本文引用的文献

1
Microglial pannexin-1 channel activation is a spinal determinant of joint pain.
Sci Adv. 2018 Aug 8;4(8):eaas9846. doi: 10.1126/sciadv.aas9846. eCollection 2018 Aug.
3
Neuronal integrity and complement control synaptic material clearance by microglia after CNS injury.
J Exp Med. 2018 Jul 2;215(7):1789-1801. doi: 10.1084/jem.20172244. Epub 2018 Jun 25.
4
Targeting toll-like receptor-4 (TLR4)-an emerging therapeutic target for persistent pain states.
Pain. 2018 Oct;159(10):1908-1915. doi: 10.1097/j.pain.0000000000001306.
5
DREADDed microglia in pain: Implications for spinal inflammatory signaling in male rats.
Exp Neurol. 2018 Jun;304:125-131. doi: 10.1016/j.expneurol.2018.03.005. Epub 2018 Mar 9.
6
Microglial Phenotypes and Functions in Multiple Sclerosis.
Cold Spring Harb Perspect Med. 2018 Feb 1;8(2):a028993. doi: 10.1101/cshperspect.a028993.
7
Microglia in neuropathic pain: cellular and molecular mechanisms and therapeutic potential.
Nat Rev Neurosci. 2018 Mar;19(3):138-152. doi: 10.1038/nrn.2018.2. Epub 2018 Feb 8.
8
Microglia and macrophages in brain homeostasis and disease.
Nat Rev Immunol. 2018 Apr;18(4):225-242. doi: 10.1038/nri.2017.125. Epub 2017 Nov 20.
10
Microglia emerge as central players in brain disease.
Nat Med. 2017 Sep 8;23(9):1018-1027. doi: 10.1038/nm.4397.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验