Bolay Hayrunnisa, Reuter Uwe, Dunn Andrew K, Huang Zhihong, Boas David A, Moskowitz Michael A
Stroke and Neurovascular Regulation Laboratory, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Nat Med. 2002 Feb;8(2):136-42. doi: 10.1038/nm0202-136.
Although the trigeminal nerve innervates the meninges and participates in the genesis of migraine headaches, triggering mechanisms remain controversial and poorly understood. Here we establish a link between migraine aura and headache by demonstrating that cortical spreading depression, implicated in migraine visual aura, activates trigeminovascular afferents and evokes a series of cortical meningeal and brainstem events consistent with the development of headache. Cortical spreading depression caused long-lasting blood-flow enhancement selectively within the middle meningeal artery dependent upon trigeminal and parasympathetic activation, and plasma protein leakage within the dura mater in part by a neurokinin-1-receptor mechanism. Our findings provide a neural mechanism by which extracerebral cephalic blood flow couples to brain events; this mechanism explains vasodilation during headache and links intense neurometabolic brain activity with the transmission of headache pain by the trigeminal nerve.
虽然三叉神经支配脑膜并参与偏头痛的发病机制,但其触发机制仍存在争议且了解甚少。在此,我们通过证明与偏头痛视觉先兆有关的皮层扩散性抑制激活三叉神经血管传入纤维,并引发一系列与头痛发展一致的皮层脑膜和脑干事件,从而建立了偏头痛先兆与头痛之间的联系。皮层扩散性抑制在三叉神经和副交感神经激活的作用下,选择性地导致脑膜中动脉内的血流持续增强,并部分通过神经激肽-1受体机制导致硬脑膜内的血浆蛋白渗漏。我们的研究结果提供了一种神经机制,通过该机制脑外头部血流与脑事件相互关联;这种机制解释了头痛期间的血管舒张,并将强烈的神经代谢性脑活动与三叉神经传递头痛疼痛联系起来。