Rothenberg S J, Selkoe D
Psychopharmacology (Berl). 1981;74(3):237-40. doi: 10.1007/BF00427101.
Changes in smooth pursuit eye tracking of horizontal sinusoidal target movement before and after up to 10 mg oral diazepam were measured electrooculographically in diazepam-naive humans. Diazepam produced a dose-dependent reduction in gain of pursuit eye movements at target frequencies of 0.4--1.6 Hz. Cross-correlation of eye and track was significantly reduced at most frequencies showing gain reduction after 10 mg diazepam. Eye-target phase relationship was not systematically altered by drug. Visual inspection of smooth pursuit tracking records showed reduced peak-to-peak amplitude of eye tracking along with replacement of smooth pursuit with saccadic pursuit, especially after 10 mg. Changes in smooth pursuit eye tracking after diazepam were similar to those changes reported in the literature associated with olivopontocerebellar atrophy and were quite unlike the changes in smooth pursuit after opiates, as previously reported. The role of cerebellar benzodiazepine binding sites in diazepam disruption of eye tracking was discussed.
在未服用过地西泮的人体中,通过眼电图测量了口服高达10毫克地西泮前后水平正弦目标运动的平稳跟踪眼球运动变化。地西泮在目标频率为0.4 - 1.6赫兹时,使跟踪眼球运动的增益呈剂量依赖性降低。在大多数频率下,眼球与轨迹的互相关性显著降低,表明服用10毫克地西泮后增益降低。药物并未系统性改变眼 - 目标相位关系。对平稳跟踪记录的视觉检查显示,眼球跟踪的峰峰值幅度减小,同时平稳跟踪被扫视跟踪取代,尤其是在服用10毫克后。地西泮后平稳跟踪眼球运动的变化与文献中报道的与橄榄脑桥小脑萎缩相关的变化相似,与先前报道的阿片类药物后平稳跟踪的变化截然不同。讨论了小脑苯二氮䓬结合位点在地西泮干扰眼球跟踪中的作用。