Kuroda S, Nakai A, Kristían T, Siesjö B K
Department of Clinical Neuroscience, Wallenberg Neuroscience Center, University of Lund, Sweden.
Stroke. 1997 Dec;28(12):2539-44. doi: 10.1161/01.str.28.12.2539.
This study was performed to assess the efficacy and the therapeutic window for the calmodulin antagonist trifluoperazine in experiments involving transient middle cerebral artery (MCA) occlusion.
Male Wistar rats were subjected to transient (2 hours) MCA occlusion by an intraluminal filament technique. Trifluoperazine (5.0 mg.kg-1) was injected intraperitoneally 5 minutes, 1 hour, or 2 hours after the induction of ischemia. Drug administration was repeated 24 hours after the first injection. Neurological scores and infarct volumes were evaluated at 48 hours of reperfusion. The effect of trifluoperazine on cortical blood flow was studied with continuous laser-Doppler flowmetry.
The median value of neurological scores in the control rats (n = 7) was 3, while those in the treated groups were 1 (5-minute group; n = 7, P < .05) and 2 (1-hour and 2-hour groups; each n = 7). The percentage of infarct volume in the control rats was 34.8 +/- 4.9% (mean +/- SD), while those in the treated groups were 11.3 +/- 12.3% (5-minute group; P < .01), 24.8 +/- 15.1% (1-hour group), and 28.8 +/- 8.3% (2-hour group). Trifluoperazine, given at 5 minutes after ischemia, had no influence on blood flow in the neocortical penumbra during and after ischemia.
The results demonstrate that trifluoperazine markedly reduces infarct volume after 2 hours of MCA occlusion when given 5 minutes after the induction of ischemia. However, the therapeutic window for trifluoperazine seems narrow since the drug had no significant effect when given after 1 or 2 hours.
本研究旨在评估钙调蛋白拮抗剂三氟拉嗪在短暂性大脑中动脉(MCA)闭塞实验中的疗效及治疗窗。
采用管腔内插入线栓技术使雄性Wistar大鼠发生短暂性(2小时)MCA闭塞。在缺血诱导后5分钟、1小时或2小时腹腔注射三氟拉嗪(5.0 mg·kg-1)。首次注射24小时后重复给药。在再灌注48小时时评估神经功能评分和梗死体积。采用连续激光多普勒血流仪研究三氟拉嗪对皮质血流的影响。
对照组大鼠(n = 7)神经功能评分的中位数为3分,而治疗组分别为1分(5分钟组;n = 7,P < 0.05)和2分(1小时组和2小时组;每组n = 7)。对照组大鼠梗死体积百分比为34.8 ± 4.9%(平均值 ± 标准差),而治疗组分别为11.3 ± 12.3%(5分钟组;P < 0.01)、24.8 ± 15.1%(1小时组)和28.8 ± 8.3%(2小时组)。缺血后5分钟给予三氟拉嗪,对缺血期间及缺血后新皮质半暗带血流无影响。
结果表明,缺血诱导后5分钟给予三氟拉嗪可显著减少MCA闭塞2小时后的梗死体积。然而三氟拉嗪的治疗窗似乎较窄,因为在1小时或2小时后给药时该药物无显著效果。