Cumberbatch M J, Hill R G, Hargreaves R J
Merck Sharp & Dohme Research Laboratories, Neuroscience Research Center, Harlow, Essex, UK.
Eur J Pharmacol. 1997 Jun 5;328(1):37-40. doi: 10.1016/s0014-2999(97)83024-5.
The 5-HT(1B/1D) receptor agonist rizatriptan constricts intracranial, extracerebral blood vessels, inhibits neurogenic vasodilation and extravasation in the meninges and is effective clinically against migraine. The present study has investigated whether rizatriptan may also have activity at 5-HT(1B/1D) receptors within the central nervous system (CNS) that contributes to its antimigraine effects. Action potentials evoked by electrical stimulation of the dura-mater were recorded extracellularly from single neurones in the trigeminal nucleus caudalis in anaesthetized rats. Rizatriptan dose dependently inhibited these nociceptive dural responses by up to 63 +/- 9% after 3 mg/kg, i.v. Rizatriptan therefore has central activity which may contribute to its efficacy against migraine headache.
5-羟色胺(5-HT)(1B/1D)受体激动剂利扎曲普坦可使颅内、脑外血管收缩,抑制软脑膜中的神经源性血管舒张和血管外渗,在临床上对偏头痛有效。本研究调查了利扎曲普坦是否也可能对中枢神经系统(CNS)内的5-HT(1B/1D)受体有活性,从而有助于其抗偏头痛作用。在麻醉大鼠的三叉神经尾核中,通过细胞外记录由硬脑膜电刺激诱发的动作电位。静脉注射3mg/kg利扎曲普坦后,其剂量依赖性地抑制这些伤害性硬脑膜反应,抑制率高达63±9%。因此,利扎曲普坦具有中枢活性,这可能有助于其对偏头痛的疗效。