Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
J Clin Invest. 2011 Sep;121(9):3528-41. doi: 10.1172/JCI45557. Epub 2011 Aug 8.
The drug development process for CNS indications is hampered by a paucity of preclinical tests that accurately predict drug efficacy in humans. Here, we show that a wide variety of CNS-active drugs induce characteristic alterations in visual stimulus-induced and/or spontaneous eye movements in mice. Active compounds included sedatives and antipsychotic, antidepressant, and antiseizure drugs as well as drugs of abuse, such as cocaine, morphine, and phencyclidine. The use of quantitative eye-movement analysis was demonstrated by comparing it with the commonly used rotarod test of motor coordination and by using eye movements to monitor pharmacokinetics, blood-brain barrier penetration, drug-receptor interactions, heavy metal toxicity, pharmacologic treatment in a model of schizophrenia, and degenerative CNS disease. We conclude that eye-movement analysis could complement existing animal tests to improve preclinical drug development.
中枢神经系统(CNS)适应证的药物开发过程受到缺乏能够准确预测药物在人体中疗效的临床前测试的阻碍。在这里,我们表明,各种 CNS 活性药物会在小鼠的视觉刺激诱导和/或自发眼球运动中引起特征性改变。活性化合物包括镇静剂和抗精神病药、抗抑郁药和抗癫痫药以及阿片类药物、可卡因、吗啡和苯环己哌啶等滥用药物。通过将其与常用的旋转轮测试进行比较,并使用眼球运动来监测药代动力学、血脑屏障穿透性、药物受体相互作用、重金属毒性、精神分裂症模型中的药物治疗以及退行性中枢神经系统疾病,证明了定量眼球运动分析的用途。我们得出结论,眼球运动分析可以补充现有的动物测试,以改善临床前药物开发。