Ettinger Ulrich, Kumari Veena, Zachariah Elizabeth, Galea Adrian, Crawford Trevor J, Corr Philip J, Taylor David, Das Mrigendra, Sharma Tonmoy
Division of Psychological Medicine, Institute of Psychiatry, UK.
Neuropsychopharmacology. 2003 Dec;28(12):2199-208. doi: 10.1038/sj.npp.1300286.
Smooth pursuit eye movement (SPEM) and antisaccade deficits are observed in the schizophrenia spectrum and have been used to study the pathophysiology as well as the genetic basis of this condition. The neurotransmitter acetylcholine has been implicated in a number of cognitive processes thought to underlie SPEM and antisaccade performance. This study investigates effects on eye movements of procyclidine, an anticholinergic drug often administered to schizophrenic patients. A total of 13 patients completed a double-blind placebo-controlled crossover design, receiving 15 mg procyclidine and placebo. Seven participants received procyclidine first and placebo second, six participants were tested in the reverse order. SPEM and antisaccade (as well as fixation and prosaccade) eye movements were recorded using infrared oculography. Results showed that procyclidine overall, relative to placebo, mildly worsened SPEM performance, as indicated by nonsignificantly reduced gain (p=0.08) and increased frequency of intrusive anticipatory saccades during pursuit (p=0.06). A significant interaction of group and order of administration indicated that procyclidine increased the rate of antisaccade reflexive errors only when administered first; the opposite pattern was observed when placebo was administered first, likely due to the operation of practice effects at second assessment. These findings indicate that acute administration of a clinically relevant dose of procyclidine leads to mild impairments in eye movement performance in schizophrenic patients, suggesting the need to consider this compound in oculomotor studies in schizophrenia. The action of this anticholinergic drug on oculomotor performance is consistent with the hypothesized role of the cholinergic system in the cognitive mechanisms of attention and working memory, processes thought to underlie SPEM and antisaccade performance. Effects of order of administration and practice on the antisaccade task suggest that these factors need to be taken into consideration in future pharmacological studies.
在精神分裂症谱系中观察到平稳跟踪眼球运动(SPEM)和反扫视缺陷,这些已被用于研究该病症的病理生理学以及遗传基础。神经递质乙酰胆碱与许多被认为是SPEM和反扫视表现基础的认知过程有关。本研究调查了丙环定(一种常用于精神分裂症患者的抗胆碱能药物)对眼球运动的影响。共有13名患者完成了双盲安慰剂对照交叉设计,接受15毫克丙环定和安慰剂。7名参与者先接受丙环定,后接受安慰剂,6名参与者按相反顺序进行测试。使用红外眼动图记录SPEM和反扫视(以及注视和顺向扫视)眼球运动。结果表明,总体而言,与安慰剂相比,丙环定使SPEM表现略有恶化,表现为增益无显著降低(p = 0.08)以及跟踪期间侵入性预期扫视频率增加(p = 0.06)。组与给药顺序的显著交互作用表明,丙环定仅在首次给药时会增加反扫视反射性错误的发生率;当首次给予安慰剂时观察到相反的模式,这可能是由于第二次评估时练习效应的作用。这些发现表明,急性给予临床相关剂量的丙环定会导致精神分裂症患者眼球运动表现出现轻度损害,这表明在精神分裂症的眼动研究中需要考虑这种化合物。这种抗胆碱能药物对眼动表现的作用与胆碱能系统在注意力和工作记忆认知机制中的假设作用一致,这些过程被认为是SPEM和反扫视表现的基础。给药顺序和练习对反扫视任务的影响表明,在未来的药理学研究中需要考虑这些因素。