Corlett P R, Honey G D, Fletcher P C
Brain Mapping Unit, Department of Psychiatry, University of Cambridge, School of Clinical Medicine, Addenbrooke's Hospital, Hills Road, Cambridge, UK.
J Psychopharmacol. 2007 May;21(3):238-52. doi: 10.1177/0269881107077716.
Recent cognitive neuropsychiatric models of psychosis emphasize the role of attentional disturbances and inappropriate incentive learning in the development of delusions. These models highlight a pre-psychotic period in which the patient experiences perceptual and attentional disruptions. Irrelevant details and numerous associations between stimuli, thoughts and percepts are imbued with inappropriate significance and the attempt to rationalize and account for these bizarre experiences results in the formation of delusions. The present paper discusses delusion formation in terms of basic associative learning processes. Such processes are driven by prediction error signals. Prediction error refers to mismatches between an organism's expectation in a given environment and what actually happens and it is signalled by both dopaminergic and glutamatergic mechanisms. Disruption of these neurobiological systems may underlie delusion formation. We review similarities between acute psychosis and the psychotic state induced by the NMDA receptor antagonist drug ketamine, which impacts upon both dopaminergic and glutamatergic function. We conclude by suggesting that ketamine may provide an appropriate model to investigate the formative stages of symptom evolution in schizophrenia, and thereby provide a window into the earliest and otherwise inaccessible aspects of the disease process.
近期关于精神病的认知神经精神病学模型强调了注意力障碍和不适当的动机学习在妄想形成过程中的作用。这些模型突出了精神病前期,在此期间患者会经历感知和注意力的紊乱。无关细节以及刺激、思想和感知之间的大量关联被赋予了不适当的重要性,而试图对这些离奇经历进行合理化解释和说明则导致了妄想的形成。本文从基本的联想学习过程角度探讨妄想的形成。此类过程由预测误差信号驱动。预测误差指的是生物体在特定环境中的预期与实际发生情况之间的不匹配,它由多巴胺能和谷氨酸能机制发出信号。这些神经生物学系统的破坏可能是妄想形成的基础。我们回顾了急性精神病与NMDA受体拮抗剂药物氯胺酮诱发的精神病状态之间的相似之处,氯胺酮会影响多巴胺能和谷氨酸能功能。我们最后提出,氯胺酮可能为研究精神分裂症症状演变的形成阶段提供一个合适的模型,从而为了解该疾病过程中最早且原本难以触及的方面提供一个窗口。