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Estrogen-Dependent Changes in Dura Mater Microvasculature Add New Insights to the Pathogenesis of Headache

机译:硬脑膜微脉管系统中雌激素依赖性变化为头痛的发病机理增添新见解

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摘要

The pathogenesis of headaches is a matter of ongoing discussion of two major theories describing it either as a vascular phenomenon resulting from vasodilation or primarily as a neurogenic process accompanied by secondary vasodilation associated with sterile neurogenic inflammation. While summarizing current views on neurogenic and vascular origins of headache, this mini review adds new insights regarding how smooth muscle-free microvascular networks, discovered within dura mater connective tissue stroma (previously thought to be “avascular”), may become a site of initial insult generating the background for the development of headache. Deficiencies in estrogen-dependent control of microvascular integrity leading to plasma protein extravasation, potential activation of perivascular and connective tissue stroma nociceptive neurons, and triggering of inflammatory responses are described. Finally, possible avenues for controlling and preventing these pathophysiological changes are discussed.
机译:头痛的发病机制是有关两个主要理论的不断讨论的问题,这些理论将其描述为由血管舒张引起的血管现象,或主要是伴随与无菌神经源性炎症相关的继发性血管舒张的神经发生过程。在总结当前关于头痛的神经源性和血管性起源的观点时,本小型综述为硬脑膜结缔组织基质(以前认为是“无血管的”)中发现的无平滑肌的微血管网络可能成为初始部位提供了新见解。侮辱产生了头痛发展的背景。描述了雌激素依赖性的微血管完整性控制的缺陷,该缺陷导致血浆蛋白外渗,血管周和结缔组织间质伤害感受神经元的潜在激活以及炎症反应的触发。最后,讨论了控制和预防这些病理生理变化的可能途径。

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