Okazawa Hidehiko, Tsuchida Tatsuro, Pagani Marco, Mori Tetsuya, Kobayashi Masato, Tanaka Fumiko, Yonekura Yoshiharu
Biomedical Imaging Research Center, University of Fukui, Fukui, Japan.
J Cereb Blood Flow Metab. 2006 Jan;26(1):92-8. doi: 10.1038/sj.jcbfm.9600167.
To investigate the vasoconstrictor effect of 5-hydroxytryptamine (5-HT1B/1D) receptor agonists for migraine treatment, changes in cerebral blood flow (CBF) and blood volume induced by rizatriptan were assessed by positron emission tomography (PET). Eleven healthy volunteers underwent PET studies before and after rizatriptan administration. Dynamic PET data were acquired after bolus injection of H2(15)O to analyze CBF and arterial-to-capillary blood volume (V0) images using the three-weighted integral method. After a baseline scan, three further acquisitions were performed at 40 to 50, 60 and 70 to 80 mins after drug administration. Global and regional differences in CBF and V0 between conditions were compared using absolute values in the whole brain and cortical regions, as well as statistical parametric mapping (SPM) analysis. The global and regional values for CBF and V0 decreased significantly after rizatriptan administration compared with the baseline condition. However, both values recovered to baseline within 80 mins after treatment. The maximal reduction in global CBF and V0 was approximately 13% of baseline value. The greatest decrease in CBF was observed approximately 60 mins after drug administration, whereas the maximal reduction in V0 was observed approximately 5 mins earlier. Statistical parametric mapping did not highlight any regional differences between conditions. Thus, in brain circulation, rizatriptan caused significant CBF and V0 decreases, which are consistent with the vasoconstrictor effect of triptans on the large cerebral arteries. The gradual recovery in the late phase from the maximal CBF and V0 decrease suggests that rizatriptan does not affect the cerebral autoregulatory response in small arteries induced by CBF reduction.
为研究5-羟色胺(5-HT1B/1D)受体激动剂治疗偏头痛的血管收缩作用,采用正电子发射断层扫描(PET)评估利扎曲普坦引起的脑血流量(CBF)和血容量变化。11名健康志愿者在利扎曲普坦给药前后接受PET研究。静脉注射H2(15)O后采集动态PET数据,采用三加权积分法分析CBF和动脉-毛细血管血容量(V0)图像。在基线扫描后,给药后40至50分钟、60分钟以及70至80分钟进行另外三次采集。使用全脑和皮质区域的绝对值以及统计参数映射(SPM)分析比较不同条件下CBF和V0的整体及区域差异。与基线状态相比,利扎曲普坦给药后CBF和V0的整体及区域值显著降低。然而,治疗后80分钟内这两个值均恢复至基线水平。CBF和V0的整体最大降幅约为基线值的13%。给药后约60分钟观察到CBF最大降幅,而V0的最大降幅则提前约5分钟出现。统计参数映射未突出显示不同条件之间的任何区域差异。因此,在脑循环中,利扎曲普坦导致CBF和V0显著降低,这与曲坦类药物对大脑大动脉的血管收缩作用一致。CBF和V0从最大降幅的后期逐渐恢复表明,利扎曲普坦不影响因CBF降低引起的小动脉脑自动调节反应。