Hansen Emma Katrine, Olesen Jes
Danish Headache Centre and Department of Neurology, University of Copenhagen, Rigshospitalet Glostrup, Denmark.
Cephalalgia. 2017 Jan;37(1):11-19. doi: 10.1177/0333102416636095. Epub 2016 Jul 11.
Background A model for the testing of novel anti-migraine drugs should preferably use healthy volunteers for ease of recruiting. Isosorbide-5-mononitrate (5-ISMN) provokes headache in healthy volunteers with some migraine features such as pulsating pain quality and aggravation by physical activity. Therefore, this headache might respond to sumatriptan, a requirement for validation of any model. The hypothesis of the present study was that sumatriptan is effective in 5-ISMN-induced headache in healthy individuals. Methods In a double-blind, randomised, crossover design, 30 healthy volunteers of both sexes received 5-ISMN 60 mg on two separate days, each day followed by oral self-administered placebo or sumatriptan 50 mg. Headache response and accompanying symptoms were registered in a questionnaire by the participants themselves. Results 5-ISMN induced a reproducible headache in all 30 participants. The headache had several migraine-like features in all participants and 20 individuals developed a migraine-like attack. Median peak headache score was 5 on both experimental days ( p = 1.00). There was no reduction, but instead an increase in headache intensity 2 hours after sumatriptan ( p = 0.003). Difference in area under the headache score curve (AUC) 0-4 hours between sumatriptan and placebo was not significant ( p = 0.30). Conclusion 5-ISMN is a very powerful inducer of migraine-like headache in healthy individuals but the headache does not respond to sumatriptan. The model is not useful for future drug testing.
新型抗偏头痛药物的测试模型最好使用健康志愿者,以便于招募。5-单硝酸异山梨酯(5-ISMN)可在具有某些偏头痛特征(如搏动性疼痛性质和体力活动加重)的健康志愿者中诱发头痛。因此,这种头痛可能对舒马曲坦有反应,这是验证任何模型的一个要求。本研究的假设是舒马曲坦对健康个体中5-ISMN诱发的头痛有效。
在一项双盲、随机、交叉设计中,30名男女健康志愿者在两个不同的日子接受60毫克5-ISMN,每天之后口服自行给药的安慰剂或50毫克舒马曲坦。参与者通过问卷记录头痛反应和伴随症状。
5-ISMN在所有30名参与者中诱发了可重复的头痛。所有参与者的头痛都有几个偏头痛样特征,20人出现了偏头痛样发作。在两个实验日,头痛峰值评分中位数均为5(p = 1.00)。舒马曲坦给药2小时后头痛强度没有降低,反而增加(p = 0.003)。舒马曲坦和安慰剂之间0至4小时头痛评分曲线下面积(AUC)的差异不显著(p = 0.30)。
5-ISMN是健康个体中偏头痛样头痛的非常强效的诱发剂,但头痛对舒马曲坦无反应。该模型对未来的药物测试无用。