Polich John, Criado José R
Cognitive Electrophysiology Laboratory, Department of Neuropharmacology TPC-10, The Scripps Research Institute, La Jolla, CA 92037, USA.
Int J Psychophysiol. 2006 May;60(2):172-85. doi: 10.1016/j.ijpsycho.2005.12.012. Epub 2006 Feb 28.
Perspectives on the P300 event-related brain potential (ERP) are reviewed by outlining the distinction between the P3a and P3b subcomponents. The critical factor for eliciting P3a is how target/standard discrimination difficulty rather than novelty modulates task processing. The neural loci of P3a and P3b generation are sketched and a theoretical model is developed. P3a originates from stimulus-driven disruption of frontal attention engagement during task processing. P3b originates when temporal-parietal mechanisms process the stimulus information for memory storage. The neuropharmacological implications of this view are then outlined by evaluating how acute and chronic use of ethanol, marijuana, and nicotine affect P3a and P3b. The findings suggest that the circuit underlying ERP generation is influenced in a different ways for acute intake and varies between chronic use levels across drugs. Theoretical implications are assessed.
通过概述P3a和P3b子成分之间的区别,对P300事件相关脑电位(ERP)的观点进行了综述。诱发P3a的关键因素是目标/标准辨别难度而非新颖性如何调节任务处理。勾勒了P3a和P3b产生的神经位点,并建立了一个理论模型。P3a源于任务处理过程中额叶注意力参与的刺激驱动性中断。当颞顶机制处理刺激信息以进行记忆存储时,P3b产生。然后通过评估乙醇、大麻和尼古丁的急性和慢性使用如何影响P3a和P3b,概述了这一观点的神经药理学意义。研究结果表明,ERP产生的潜在回路在急性摄入时受到不同方式的影响,并且在不同药物的慢性使用水平之间存在差异。评估了理论意义。