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

Frontiers in Neurology Pub Date : 2017-10-18 eCollection Date: 2017-01-01 DOI:10.3389/fneur.2017.00549
Olga V Glinskii, Virginia H Huxley, Vladislav V Glinsky
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引用次数: 7

Abstract

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.

Abstract Image

Abstract Image

硬脑膜微血管的雌激素依赖性改变为头痛的发病机制提供了新的见解。
头痛的发病机制是两种主要理论的持续讨论,它们要么是由血管舒张引起的血管现象,要么主要是伴随继发性血管舒张的神经源性过程,并伴有无菌神经源性炎症。在总结目前关于头痛的神经源性和血管起源的观点的同时,这篇小型综述增加了新的见解,即在硬脑膜结缔组织基质中发现的无平滑肌微血管网络(以前被认为是“无血管的”)如何成为产生头痛发展背景的初始损伤部位。雌激素依赖控制微血管完整性的缺陷导致血浆蛋白外渗,血管周围和结缔组织间质伤害性神经元的潜在激活,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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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