Department of Anesthesia, Critical Care and Pain Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115
Department of Anesthesia, Critical Care and Pain Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115.
J Neurosci. 2019 Mar 6;39(10):1867-1880. doi: 10.1523/JNEUROSCI.2153-18.2018. Epub 2019 Jan 8.
Current understanding of the origin of occipital headache falls short of distinguishing between cause and effect. Most preclinical studies involving trigeminovascular neurons sample neurons that are responsive to stimulation of dural areas in the anterior 2/3 of the cranium and the periorbital skin. Hypothesizing that occipital headache may involve activation of meningeal nociceptors that innervate the posterior ⅓ of the dura, we sought to map the origin and course of meningeal nociceptors that innervate the posterior dura overlying the cerebellum. Using AAV-GFP tracing and single-unit recording techniques in male rats, we found that neurons in C2-C3 DRGs innervate the dura of the posterior fossa; that nearly half originate in DRG neurons containing CGRP and TRPV1; that nerve bundles traverse suboccipital muscles before entering the cranium through bony canals and large foramens; that central neurons receiving nociceptive information from the posterior dura are located in C2-C4 spinal cord and that their cutaneous and muscle receptive fields are found around the ears, occipital skin and neck muscles; and that administration of inflammatory mediators to their dural receptive field, sensitize their responses to stimulation of the posterior dura, peri-occipital skin and neck muscles. These findings lend rationale for the common practice of attempting to alleviate migraine headaches by targeting the greater and lesser occipital nerves with anesthetics. The findings also raise the possibility that such procedures may be more beneficial for alleviating occipital than non-occipital headaches and that occipital migraines may be associated more closely with cerebellar abnormalities than in non-occipital migraines. Occipital headaches are common in both migraine and non-migraine headaches. Historically, two distinct scenarios have been proposed for such headaches; the first suggests that the headaches are caused by spasm or tension of scalp, shoulders, and neck muscles inserted in the occipital region, whereas the second suggests that these headaches are initiated by activation of meningeal nociceptors. The current study shows that the posterior dura overlying the cerebellum is innervated by cervicovascular neurons in C2 DRG whose axons reach the posterior dura through multiple intracranial and extracranial pathways, and sensitization of central cervicovascular neurons from the posterior dura can result in hyper-responsiveness to stimulation of neck muscles. The findings suggest that the origin of occipital and frontal migraine may differ.
目前对于枕部头痛的发病机制尚未明确,其原因和结果仍难以区分。大多数涉及三叉神经血管神经元的临床前研究都对前颅 2/3 和眶周皮肤的硬脑膜区域刺激有反应的神经元进行采样。我们假设枕部头痛可能涉及脑膜伤害感受器的激活,这些伤害感受器支配小脑后部的硬脑膜,因此我们试图绘制支配小脑后部硬脑膜的脑膜伤害感受器的起源和分布。我们使用雄性大鼠的 AAV-GFP 示踪和单个神经元记录技术,发现 C2-C3DRG 中的神经元支配颅后窝硬脑膜;其中近一半来源于含有 CGRP 和 TRPV1 的 DRG 神经元;神经束穿过枕下肌,然后通过骨管和大孔进入颅腔;接收来自后颅硬脑膜伤害性信息的中枢神经元位于 C2-C4 脊髓,其皮肤和肌肉感受野位于耳朵、枕部皮肤和颈部肌肉周围;向其硬脑膜感受野给予炎症介质可使其对后颅、 peri-occipital 皮肤和颈部肌肉的刺激反应敏感。这些发现为常见的做法提供了合理的依据,即用麻醉剂靶向枕大神经和枕小神经来缓解偏头痛。这些发现还提出了这样一种可能性,即此类手术可能更有利于缓解枕部而非非枕部头痛,并且枕部偏头痛可能与小脑异常的相关性比非枕部偏头痛更强。枕部头痛在偏头痛和非偏头痛中都很常见。从历史上看,对于这种头痛提出了两种截然不同的情况;第一种情况表明,头痛是由插入枕部的头皮、肩部和颈部肌肉的痉挛或紧张引起的,而第二种情况表明,这些头痛是由脑膜伤害感受器的激活引起的。本研究表明,小脑后部硬脑膜由 C2DRG 中的血管神经支配,其轴突通过多种颅内和颅外途径到达后颅硬脑膜,来自后颅硬脑膜的中枢血管神经的敏化可导致对颈部肌肉刺激的过度反应。这些发现表明,枕部和额部偏头痛的起源可能不同。