Department of Internal Medicine, Lund University Hospital, Lund, Sweden.
Cephalalgia. 2010 Oct;30(10):1233-40. doi: 10.1177/0333102410362122. Epub 2010 Mar 26.
Calcitonin gene-related peptide (CGRP) is a neuronal messenger in intracranial sensory nerves and is considered to play a significant role in migraine pathophysiology.
We investigated the effect of the CGRP receptor antagonist, telcagepant, on CGRP-induced cranial vasodilatation in human isolated cerebral and middle meningeal arteries. We also studied the expression of the CGRP receptor components in cranial arteries with immunocytochemistry. Concentration response curves to αCGRP were performed in human isolated cerebral and middle meningeal arteries in the absence or presence of telcagepant. Arterial slices were stained for RAMP1, CLR and actin in a double immunofluorescence staining.
In both arteries, we found that: (i) telcagepant was devoid of any contractile or relaxant effects per se; (ii) pretreatment with telcagepant antagonised the αCGRP-induced relaxation in a competitive manner; and (iii) immunohistochemistry revealed expression and co-localisation of CLR and RAMP1 in the smooth muscle cells in the media layer of both arteries.
Our findings provide morphological and functional data on the presence of CGRP receptors in cerebral and meningeal arteries, which illustrates a possible site of action of telcagepant in the treatment of migraine.
降钙素基因相关肽(CGRP)是颅内感觉神经中的一种神经元信使,被认为在偏头痛病理生理学中发挥重要作用。
我们研究了 CGRP 受体拮抗剂,telcagepant,对人离体大脑和脑膜动脉中 CGRP 诱导的颅脑血管扩张的影响。我们还通过免疫细胞化学研究了颅动脉中 CGRP 受体成分的表达。在不存在或存在 telcagepant 的情况下,在人离体大脑和脑膜动脉中进行 αCGRP 的浓度反应曲线。动脉切片在双重免疫荧光染色中针对 RAMP1、CLR 和肌动蛋白进行染色。
在这两种动脉中,我们发现:(i)telcagepant 本身没有任何收缩或舒张作用;(ii)telcagepant 的预处理以竞争性方式拮抗 αCGRP 诱导的舒张;(iii)免疫组织化学显示 CLR 和 RAMP1 在两种动脉中层平滑肌细胞中的表达和共定位。
我们的发现提供了 CGRP 受体在大脑和脑膜动脉中存在的形态学和功能数据,这说明了 telcagepant 在偏头痛治疗中的可能作用部位。