Williamson D J, Shepheard S L, Hill R G, Hargreaves R J
Department of Pharmacology, Merck Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Harlow, Essex, UK.
Eur J Pharmacol. 1997 Jun 5;328(1):61-4. doi: 10.1016/s0014-2999(97)83028-2.
These studies in anaesthetised rats showed, using intravital microscopy, that the novel anti-migraine agent, rizatriptan, significantly reduced electrically stimulated dural vasodilation but had no effect on increases in dural vessel diameter produced by exogenous substance P or calcitonin gene-related peptide (CGRP). Rizatriptan also significantly inhibited dural plasma protein extravasation produced by high intensity electrical stimulation of the trigeminal ganglion. We suggest that rizatriptan inhibits the release of sensory neuropeptides from perivascular trigeminal nerves to prevent neurogenic vasodilation and extravasation in the dura mater. These prejunctional inhibitory effects may be involved in the anti-migraine action of rizatriptan.
这些针对麻醉大鼠的研究通过活体显微镜观察显示,新型抗偏头痛药物利扎曲普坦能显著减轻电刺激引起的硬脑膜血管舒张,但对外源性P物质或降钙素基因相关肽(CGRP)引起的硬脑膜血管直径增加没有影响。利扎曲普坦还能显著抑制三叉神经节高强度电刺激引起的硬脑膜血浆蛋白外渗。我们认为,利扎曲普坦可抑制血管周围三叉神经感觉神经肽的释放,以防止硬脑膜中神经源性血管舒张和血浆蛋白外渗。这些突触前抑制作用可能与利扎曲普坦的抗偏头痛作用有关。