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首页> 外文期刊>The Journal of Physiology >Capsaicin-sensitive neurogenic sensory vasodilatation in the dura mater of the rat.
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Capsaicin-sensitive neurogenic sensory vasodilatation in the dura mater of the rat.

机译:大鼠硬脑膜中辣椒素敏感的神经源性感觉血管舒张。

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The neurogenic sensory vascular responses of the dura mater encephali are considered to contribute significantly to the mechanisms of meningeal nociception and headache. Although the fundamental role of capsaicin-sensitive afferent nerves in the development of the neurogenic inflammatory responses of a variety of tissues is well established, their participation in meningeal vascular reactions is unclear. In the present study, the effects of the topical application of capsaicin on the dural blood flow and on the morphology of the dural nerve fibres were examined in control and capsaicin-pretreated rats by means of laser Doppler flowmetry and electron microscopy, respectively. In the control rats, the dural application of capsaicin at concentrations of 50 and 100 nM induced significant increases in blood flow in the branches of the medial meningeal artery. This capsaicin-induced vasodilatation was abolished by capsazepine, a transient receptor potential vanilloid 1 (TRPV1) receptor antagonist, and by hCGRP8-37, a calcitonin gene-related peptide (CGRP) receptor antagonist. Administration of capsaicin at higher concentrations (1 and 10 microM) resulted in marked, dose-dependent decreases in dural blood flow. The capsaicin-induced vasodilatation was abolished, whereas vasoconstriction was augmented, by systemic pretreatment of the animals with capsaicin. Electron microscopy revealed degenerating unmyelinated axons in the dura mater after an acute exposure to capsaicin (10 microM), providing support for the existence and possible functional role of capsaicin-sensitive dural afferent nerves. The results indicate that capsaicin-induced vasodilatation in the rat dura mater is mediated by the release of CGRP from the sensory nerves, whereas the vasoconstrictor response may be attributed to a direct action of capsaicin on the vascular smooth muscle. The present study demonstrates for the first time that capsaicin-sensitive nociceptive afferent nerves contribute significantly to the dural vasodilatory responses andsuggests an important role in meningeal nociception.
机译:硬脑膜的神经源性感觉血管反应被认为对脑膜伤害感受和头痛的机制有重要贡献。尽管辣椒素敏感性传入神经在各种组织的神经源性炎症反应的发展中起着基本作用,但它们是否参与脑膜血管反应尚不清楚。在本研究中,分别通过激光多普勒血流仪和电子显微镜检查了对照和辣椒素预处理大鼠中局部应用辣椒素对硬脑膜血流和硬脑膜神经纤维形态的影响。在对照大鼠中,硬膜外应用浓度为50和100 nM的辣椒素可引起内侧脑膜动脉分支血流量显着增加。辣椒素诱导的血管扩张被短暂的受体电位类香草酸1(TRPV1)受体拮抗剂辣椒素和降钙素基因相关肽(CGRP)受体hCGRP8-37消除。较高浓度(1和10 microM)的辣椒素给药导致硬脑膜血流量显着,剂量依赖性降低。通过用辣椒素对动物进行全身预处理,消除了辣椒素引起的血管舒张,而增加了血管收缩。电镜显示急性暴露于辣椒素(10 microM)后硬脑膜中未髓鞘的轴突变性,为辣椒素敏感的硬脑膜传入神经的存在和可能的功能提供了支持。结果表明,辣椒素诱导的大鼠硬脑膜血管舒张是由感觉神经释放CGRP介导的,而血管收缩反应可能归因于辣椒素对血管平滑肌的直接作用。本研究首次证明了辣椒素敏感的伤害感受传入神经对硬脑膜血管舒张反应做出了重要贡献,并提示其在脑膜伤害感受中的重要作用。

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