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偏头痛发生器再探:连续扫描偏头痛周期 30 天和 3 次自发性发作。

The migraine generator revisited: continuous scanning of the migraine cycle over 30 days and three spontaneous attacks.

机构信息

Department of Systems Neuroscience, Center for Experimental Medicine, University Medical Center Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.

Department of Systems Neuroscience, Center for Experimental Medicine, University Medical Center Eppendorf, Martinistr. 52, 20246 Hamburg, Germany

出版信息

Brain. 2016 Jul;139(Pt 7):1987-93. doi: 10.1093/brain/aww097. Epub 2016 May 5.


DOI:10.1093/brain/aww097
PMID:27190019
Abstract

Functional imaging using positron emission tomography and later functional magnetic resonance imaging revealed a particular brainstem area that is believed to be specifically activated in migraine during, but not outside of the attack, and consequently has been coined the 'migraine generator'. However, the pathophysiological concept behind this term is not undisputed and typical migraine premonitory symptoms such as fatigue and yawning, but also a typical association of attacks to circadian and menstrual cycles, all make the hypothalamus a possible regulating region of migraine attacks. Neuroimaging studies investigating native human migraine attacks however are scarce and for methodological but also clinical reasons there are currently no studies investigating the last 24 h before headache onset. Here we report a migraine patient who had magnetic resonance imaging every day for 30 days, always in the morning, to cover, using functional imaging, a whole month and three complete, untreated migraine attacks. We found that hypothalamic activity as a response to trigeminal nociceptive stimulation is altered during the 24 h prior to pain onset, i.e. increases towards the next migraine attack. More importantly, the hypothalamus shows altered functional coupling with the spinal trigeminal nuclei and the region of the migraine generator, i.e. the dorsal rostral pons during the preictal day and the pain phase of native human migraine attacks. These data suggest that although the brainstem is highly linked to the migraine biology, the real driver of attacks might be the functional changes in hypothalamo-brainstem connectivity.

摘要

使用正电子发射断层扫描和后来的功能磁共振成像进行功能成像,揭示了一个特定的脑干区域,据信在偏头痛发作期间(而非发作之外)特异性激活,因此被称为“偏头痛发生器”。然而,这个术语背后的病理生理概念并非没有争议,典型的偏头痛前驱症状,如疲劳和打哈欠,以及攻击与昼夜节律和月经周期的典型关联,都使得下丘脑成为偏头痛发作的可能调节区域。然而,调查原发性人类偏头痛发作的神经影像学研究却很少,由于方法学和临床原因,目前尚无研究调查头痛发作前 24 小时。在这里,我们报告了一位偏头痛患者,她在 30 天内每天早上进行磁共振成像,以使用功能成像覆盖整整一个月和三次完整的、未经治疗的偏头痛发作。我们发现,三叉神经伤害性刺激前 24 小时,即偏头痛发作前,下丘脑对疼痛的反应性活动发生改变,即朝着下一次偏头痛发作增加。更重要的是,在下一个偏头痛发作前一天和原发性人类偏头痛发作的疼痛阶段,下丘脑显示出与三叉神经核和偏头痛发生器区域(即颅后背部桥脑)改变的功能耦合。这些数据表明,尽管脑干与偏头痛生物学高度相关,但攻击的真正驱动力可能是下丘脑-脑干连接的功能变化。

相似文献

[1]
The migraine generator revisited: continuous scanning of the migraine cycle over 30 days and three spontaneous attacks.

Brain. 2016-5-5

[2]
Understanding migraine as a cycling brain syndrome: reviewing the evidence from functional imaging.

Neurol Sci. 2017-5

[3]
Longitudinal Neuroimaging over 30 Days: Temporal Characteristics of Migraine.

Ann Neurol. 2020-2-18

[4]
Of generators, networks and migraine attacks.

Curr Opin Neurol. 2017-6

[5]
Trigeminal nociceptive transmission in migraineurs predicts migraine attacks.

J Neurosci. 2011-2-9

[6]
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Cephalalgia. 2019-8-29

[7]
Functional connectivity of hypothalamus in chronic migraine with medication overuse.

Cephalalgia. 2019-3-5

[8]
Hypothalamic activation in spontaneous migraine attacks.

Headache. 2007

[9]
Altered regional cerebral blood flow and hypothalamic connectivity immediately prior to a migraine headache.

Cephalalgia. 2020-4

[10]
Hypothalamus as a mediator of chronic migraine: Evidence from high-resolution fMRI.

Neurology. 2017-5-23

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Neurol Ther. 2025-9-6

[2]
Atrophy of hypothalamic subregions increases migraine risk: cross-sectional study and mendelian randomization analysis.

J Headache Pain. 2025-8-6

[3]
Disrupting the Clock: Meta-Analysis of Irregular Night Shifts and Migraine, Proposing Shift Work Migraine Disorder with Chronobiology Strategies.

medRxiv. 2025-8-1

[4]
Ex vivo stimulation of the trigeminal nucleus caudalis induces peripheral CGRP release in the trigeminal ganglion and reveals a distinct dopamine-endocannabinoid mechanism relevant to migraine.

J Headache Pain. 2025-6-16

[5]
Repurposed versus disease-specific medicinals for the prophylaxis of migraine: an updated systematic review.

Pain Manag. 2025-7

[6]
Ubrogepant for the treatment of migraine prodromal symptoms: an exploratory analysis from the randomized phase 3 PRODROME trial.

Nat Med. 2025-5-12

[7]
The role and interaction of hypothalamic-related neurotransmitters in migraine.

J Headache Pain. 2025-5-12

[8]
Acute neuroendocrine challenge elicits enhanced cortisol response and parallel transcriptomic changes in patients with migraine.

Pain Rep. 2025-5-1

[9]
Evaluating the Role of Coenzyme Q10 in Migraine Therapy-A Narrative Review.

Antioxidants (Basel). 2025-3-6

[10]
Cluster Headache and Migraine Shared and Unique Insights: Neurophysiological Implications, Neuroimaging, and Biomarkers: A Comprehensive Review.

J Clin Med. 2025-3-21

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