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The effects of ketamine and risperidone on eye movement control in healthy volunteers

机译:氯胺酮和利培酮对健康志愿者眼球运动的控制

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The non-competitive N -methyl-D-aspartate receptor antagonist ketamine leads to transient psychosis-like symptoms and impairments in oculomotor performance in healthy volunteers. This study examined whether the adverse effects of ketamine on oculomotor performance can be reversed by the atypical antipsychotic risperidone. In this randomized double-blind, placebo-controlled study, 72 healthy participants performed smooth pursuit eye movements (SPEM), prosaccades (PS) and antisaccades (AS) while being randomly assigned to one of four drug groups (intravenous 100?ng?ml?1 ketamine, 2?mg oral risperidone, 100?ng?ml?1 ketamine plus 2?mg oral risperidone, placebo). Drug administration did not lead to harmful adverse events. Ketamine increased saccadic frequency and decreased velocity gain of SPEM (all P P ?0.07). An effect of risperidone was observed for amplitude gain and peak velocity of PS and AS, indicating hypometric gain and slower velocities compared with placebo (both P ?0.04). No ketamine by risperidone interactions were found (all P ?0.26). The results confirm that the administration of ketamine produces oculomotor performance deficits similar in part to those seen in schizophrenia. The atypical antipsychotic risperidone did not reverse ketamine-induced deteriorations. These findings do not support the cognitive enhancing potential of risperidone on oculomotor biomarkers in this model system of schizophrenia and point towards the importance of developing alternative performance-enhancing compounds to optimise pharmacological treatment of schizophrenia.
机译:非竞争性N-甲基-D-天冬氨酸受体拮抗剂氯胺酮会导致短暂的精神病样症状,并损害健康志愿者的动眼能力。这项研究检查了非典型抗精神病药物利培酮是否可以逆转氯胺酮对动眼功能的不利影响。在这项随机,双盲,安慰剂对照的研究中,有72位健康参与者随机分为四个药物组(静脉注射100?ng?ml)之一进行了平滑追随眼球运动(SPEM),刺激性(PS)和镇静性(AS)。 ?1 氯胺酮,2?mg口服利培酮,100?ng?ml ?1 氯胺酮加2?mg口服利培酮,安慰剂。药物管理未导致有害的不良事件。氯胺酮增加声频率,降低SPEM的速度增益(所有P P≤0.07)。观察到利培酮对PS和AS的振幅增益和峰值速度有影响,这表明与安慰剂相比,虚高增益和较慢的速度(均P≤0.04)。未发现通过利培酮相互作用产生的氯胺酮(所有P = 0.26)。结果证实,氯胺酮的施用会引起动眼功能障碍,部分类似于精神分裂症。非典型抗精神病药物利培酮没有逆转氯胺酮引起的恶化。这些发现不支持利培酮在这种精神分裂症模型系统中对动眼生物标记物的认知增强潜力,并指出开发替代性能增强化合物以优化精神分裂症药理治疗的重要性。

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