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偏头痛:疼痛源自何处以及如何产生?

Migraine: where and how does the pain originate?

作者信息

Messlinger Karl

机构信息

Institute of Physiology and Pathophysiology, University of Erlangen-Nürnberg, Erlangen, Germany.

出版信息

Exp Brain Res. 2009 Jun;196(1):179-93. doi: 10.1007/s00221-009-1756-y. Epub 2009 Mar 14.

DOI:10.1007/s00221-009-1756-y
PMID:19288089
Abstract

Migraine is a complex neurological disease with a genetic background. Headache is the most prominent and clinically important symptom of migraine but its origin is still enigmatic. Numerous clinical, histochemical, electrophysiological, molecular and genetical approaches form a puzzle of findings that slowly takes shape. The generation of primary headaches like migraine pain seems to be the consequence of multiple pathophysiological changes in meningeal tissues, the trigeminal ganglion, trigeminal brainstem nuclei and descending inhibitory systems, based on specific characteristics of the trigeminovascular system. This contribution reviews the current discussion of where and how the migraine pain may originate and outlines the experimental work to answer these questions.

摘要

偏头痛是一种具有遗传背景的复杂神经系统疾病。头痛是偏头痛最突出且临床上最重要的症状,但其起源仍然成谜。众多临床、组织化学、电生理、分子和遗传学方法形成了一幅逐渐成形的研究结果拼图。基于三叉神经血管系统的特定特征,像偏头痛疼痛这样的原发性头痛的产生似乎是脑膜组织、三叉神经节、三叉神经脑干核以及下行抑制系统中多种病理生理变化的结果。本论文综述了当前关于偏头痛疼痛可能起源于何处以及如何产生的讨论,并概述了为回答这些问题所开展的实验工作。

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2
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本文引用的文献

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Increase in NADPH-diaphorase-positive and neuronal NO synthase immunoreactive neurons in the rat spinal trigeminal nucleus following infusion of a NO donor--evidence for a feed-forward process in NO production involved in trigeminal nociception.在大鼠三叉神经脊束核中,注入一氧化氮供体后,烟酰胺腺嘌呤二核苷酸磷酸黄递酶阳性和神经元型一氧化氮合酶免疫反应性神经元增加——三叉神经痛觉感受中一氧化氮产生的前馈过程的证据。
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Calcitonin gene-related peptide receptor inhibition reduces neuronal activity induced by prolonged increase in nitric oxide in the rat spinal trigeminal nucleus.降钙素基因相关肽受体抑制可降低大鼠三叉神经脊束核中一氧化氮长期增加所诱导的神经元活动。
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吸烟对女性偏头痛发展的影响:韩国全国队列研究。
JMIR Public Health Surveill. 2024 Aug 23;10:e58105. doi: 10.2196/58105.
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Inflammatory response of leptomeninges to a single cortical spreading depolarization.软脑膜对单个皮质扩散性抑制的炎症反应。
J Headache Pain. 2024 Jul 16;25(1):113. doi: 10.1186/s10194-024-01823-1.
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Mechanosensitive receptors in migraine: a systematic review.偏头痛中的机械敏感受体:系统评价。
J Headache Pain. 2024 Jan 15;25(1):6. doi: 10.1186/s10194-023-01710-1.
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Double-blind, randomized, placebo-controlled study to evaluate erenumab-specific central effects: an fMRI study.双盲、随机、安慰剂对照研究评估依瑞奈umab 的中枢作用:一项 fMRI 研究。
J Headache Pain. 2024 Jan 9;25(1):5. doi: 10.1186/s10194-023-01709-8.
7
Potent dual MAGL/FAAH inhibitor AKU-005 engages endocannabinoids to diminish meningeal nociception implicated in migraine pain.强效双重 MAGL/FAAH 抑制剂 AKU-005 通过作用于内源性大麻素来减轻偏头痛疼痛中涉及的脑膜伤害感受。
J Headache Pain. 2023 Apr 11;24(1):38. doi: 10.1186/s10194-023-01568-3.
8
FM1-43 Dye Memorizes Piezo1 Activation in the Trigeminal Nociceptive System Implicated in Migraine Pain.FM1-43 染料记忆三叉神经痛觉系统中的 Piezo1 激活与偏头痛疼痛有关。
Int J Mol Sci. 2023 Jan 14;24(2):1688. doi: 10.3390/ijms24021688.
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HCN2 Ion Channels Drive Pain in Rodent Models of Migraine.HCN2 离子通道驱动偏头痛啮齿动物模型的疼痛。
J Neurosci. 2022 Oct 5;42(40):7513-7529. doi: 10.1523/JNEUROSCI.0721-22.2022. Epub 2022 Sep 2.
10
Role of ATP in migraine mechanisms: focus on P2X3 receptors.ATP 在偏头痛发病机制中的作用:聚焦于 P2X3 受体。
J Headache Pain. 2023 Jan 3;24(1):1. doi: 10.1186/s10194-022-01535-4.
Nitroglycerin facilitates calcitonin gene-related peptide-induced behavior.硝酸甘油可促进降钙素基因相关肽诱导的行为。
Neuroreport. 2008 Aug 27;19(13):1307-11. doi: 10.1097/WNR.0b013e32830b0f9d.
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Tactile-induced ultrasonic vocalization in the rat: a novel assay to assess anti-migraine therapies in vivo.大鼠触觉诱发的超声发声:一种评估体内抗偏头痛疗法的新方法。
Cephalalgia. 2008 Jul;28(7):723-33. doi: 10.1111/j.1468-2982.2008.01582.x. Epub 2008 May 21.
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J Headache Pain. 2008 Apr;9(2):57-69. doi: 10.1007/s10194-008-0026-x. Epub 2008 Mar 15.
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Neuropeptides. 2008 Jun;42(3):311-7. doi: 10.1016/j.npep.2008.01.002. Epub 2008 Mar 6.
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