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P300的生物学决定因素:巴比妥酸盐对潜伏期和波幅的影响。

Biological determinants of P300: the effects of a barbiturate on latency and amplitude.

作者信息

Fowler B, Mitchell I

机构信息

Graduate Programme in Exercise and Health Science, York University, Ontario, Canada.

出版信息

Biol Psychol. 1997 Aug 22;46(2):113-24. doi: 10.1016/s0301-0511(97)05253-8.

Abstract

Polich & Kok (1995) (Biological Psychology, 41, 103-146) have recently argued that P300 is not only sensitive to specific 'cognitive' variables, but also to non-specific biological processes such as arousal. Fluctuations in arousal are said to be indexed by an inverse relationship between latency and amplitude. We tested this hypothesis with a drug that decreases arousal-the barbiturate secobarbital sodium. Twelve subjects performed a visual 80-20% oddball task at two levels of stimulus quality and after ingesting the drug (2.9 mg/kg body weight) or a placebo. Reaction time (RT) and P300 were collected simultaneously and the latter was analyzed on both a single trial and average basis. The RT results confirmed that secobarbital interacts with stimulus quality. Secobarbital slowed single trial P300 by about half as much as RT, and this slowing was additive with stimulus quality. Thus the two measures dissociated. Secobarbital did not influence P300 amplitude. Average P300 revealed the same pattern of results, although the size of the latency effects was somewhat attenuated. RT and P300 latency were more strongly correlated than P300 latency and amplitude. We propose that P300 latency reflected the slowing of stimulus evaluation produced by the depressant properties of the drug, and that fluctuations in arousal are not necessarily associated with a simple inverse relationship between P300 latency and amplitude.

摘要

波利奇和科克(1995年)(《生物心理学》,第41卷,第103 - 146页)最近指出,P300不仅对特定的“认知”变量敏感,而且对诸如唤醒等非特定的生物过程也敏感。据说唤醒的波动通过潜伏期和波幅之间的反比关系来体现。我们用一种能降低唤醒水平的药物——巴比妥酸盐速可巴比妥钠来检验这一假设。12名受试者在两种刺激质量水平下执行视觉80 - 20%的异常刺激任务,并且在摄入药物(2.9毫克/千克体重)或安慰剂后进行该任务。同时收集反应时间(RT)和P300,并且对后者在单次试验和平均基础上进行分析。RT结果证实速可巴比妥与刺激质量相互作用。速可巴比妥使单次试验的P300减慢的程度约为RT的一半,并且这种减慢与刺激质量是相加的。因此这两种测量结果出现了分离。速可巴比妥不影响P300波幅。平均P300显示出相同的结果模式,尽管潜伏期效应的大小有所减弱。RT和P300潜伏期的相关性比P300潜伏期和波幅的相关性更强。我们认为P300潜伏期反映了药物抑制特性导致的刺激评估减慢,并且唤醒的波动不一定与P300潜伏期和波幅之间的简单反比关系相关。

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