The effects of a heterotopic cold pain stimulus applied to the hand on the scalp-recorded negative difference potential (NDP) and subjective pain ratings elicited by electrical stimulation of the sural nerve were examined in 24 participants. Our previous work strongly suggests that the NDP is generated in part by the cognitive division of the anterior cingulate cortex (ACCcd). The latency and magnitude of the ACCcd activity were estimated from the NDP and from the dipole source localization analysis of the NDP. As expected, the sural nerve pain ratings were smaller in the cold pain condition than in the control condition. The ACCcd activity underlying the 125-ms peak of the NDP did not change across conditions, whereas the ACCcd activity underlying the 210-ms NDP peak was largest in the cold pain condition. The dissociation between pain-evoked ACCcd activity and pain ratings observed here and elsewhere suggest that not all of the nociresponsive neurons in the ACCcd are involved in pain sensation. Rather, differences in the cognitive demands of the control and cold pain conditions suggest that the pain-evoked 210-ms ACCcd activity reflects response selection processes, perhaps response competition monitoring.

This study examined stress cortisol responses and cognitive performance. We initially measured cortisol responses of 40 right-handed healthy male volunteers to counterbalanced mental arithmetic and public speaking stressors. We then examined the relationship between cortisol reactivity and dichotic listening and mental arithmetic performance. High cortisol responders made more errors and completed fewer mental arithmetic items than low reactors. On dichotic listening, high responders tended toward better performance in all conditions and to both ears. High responders showed better performance to the right ear in the forced right than in the nonforced condition, whereas no difference between these conditions was found in low responders. High cortisol responders may have an increased focus on sensory stimuli and a decreased allocation of resources to working memory tasks.

The present study was aimed at deciphering whether the delay in choice reaction time (RT) and the silent period (SP) caused by transcranial magnetic stimulation (TMS) of the motor cortex in the ongoing electromyogram are due to the same physiological mechanism. To this end, the effect of TMS was studied in 6 healthy volunteers performing a between-hand choice RT task. Specific predictions were derived from a logic inspired from the “postponed stages” hypothesis (Pashler & Johnson, 1989). This logic predicts a correlation between SP duration and RT when the stimulated cortex is involved in the response, and a stronger correlation when the stimulation is delivered later during the RT interval. The effect of TMS on RT was twofold: At early stimulation times, the stimulation shortened the RT and this effect was independent of the involvement of the stimulated motor cortex in the subsequent response. At later stimulation times, TMS had a disruptive effect, provided that the stimulated cortex was involved in the response. When the stimulated cortex was involved in the response, there was a correlation between SP and RT; this correlation was stronger when the stimulation occurred later. In contrast, there was no correlation between these two variables when the stimulated cortex was not involved.

AC amplifiers can introduce significant distortions into the low frequency and DC components of recorded electrophysiological data such as event-related potentials (ERPs). Methods for correcting such distortions (i.e., estimating the waveform of the original data) after the data have been amplified and recorded rely on an accurate estimate of the amplifier's time constant (TC). We show that the filter characteristics of AC amplifiers in at least some commercially available ERP recording instruments may vary considerably across individual channels, even when each houses an identical AC amplifier circuit. Clearly, distortion correction methods must take this variability into account. We propose an empirical means of estimating the correct TC value. This approach yields more accurate correction than those based on TCs calculated analytically.

We investigated the inhibitory regulation of perceptual–motor processing streams in a task that switched between spatially compatible and incompatible stimulus–response mappings. Thirty male and female college-aged participants performed a reaction time (RT) task in which the response was either spatially compatible or not depending on a cue immediately preceding the stimulus. The cue-to-stimulus interval (CI) was either 50 or 500 ms. Incompatible mapping yielded the typical slower responses than compatible mapping at 500 ms, but not at 50 ms. Changes in cardiac interbeat interval (IBI) and performance suggested that automatic responses to compatible stimuli were suppressed at 50 ms. Both performance and IBI changes as well as individual differences in these measures suggested a precue preparatory schema or set biased toward suppressing the compatible mapping. An alternate hypothesis of a cue-induced suppression was questioned. The results illustrate the operation of different supervisory processes in the anticipatory and online control of action.

This study investigated cognitive and neural processes involved in gap filling during on-line sentence comprehension. Electroencephalogram (EEG) coherences were used to demonstrate that increases in the synchronization of neural activity in different cortical regions occur during gap filling when load in semantic working memory is high due to semantically unrelated words in the filler-gap interval. Sentences could either require gap filling at a verb or not, and the nouns preceding the verb could be either semantically related or unrelated. In the unrelated but not related condition, coherences in the beta band were larger during verb processing for sentences requiring gap filling compared to sentences not requiring gap filling. The coherence changes involved linkages between frontal and posterior temporal-parietal sites in both hemispheres. These results further indicate that semantic working memory is involved in the process of gap filling.

There is growing evidence that in human skin conductance response (SCR) conditioning positive patterning (A−, B−, AB+) and negative patterning (A+, B+, AB−) are solved by applying two different rules. The present experiments investigated whether the representations of such rules are specific or general with regard to outcomes and response systems. In Experiment 1, we investigated SCR and eyelid conditioning with different types of training administered in an interleaved fashion. We found that positive patterning SCR conditioning interfered with negative patterning SCR conditioning, whereas eyeblink conditioning had no effect on SCR conditioning. In Experiment 2, in which eyeblink and SCR conditioning were administered in sequential fashion, the same result was obtained. We conclude that the rules involved in solving patterning tasks might be specific to outcomes and/or response systems.

Hemodynamic and electrophysiological studies indicate differential brain response to emotionally arousing, compared to neutral, pictures. The time course and source distribution of electrocortical potentials in response to emotional stimuli, using a high-density electrode (129-sensor) array were examined here. Event-related potentials (ERPs) were recorded while participants viewed pleasant, neutral, and unpleasant pictures. ERP voltages were examined in six time intervals, roughly corresponding to P1, N1, early P3, late P3 and a slow wave window. Differential activity was found for emotional, compared to neutral, pictures at both of the P3 intervals, as well as enhancement of later posterior positivity. Source space projection was performed using a minimum norm procedure that estimates the source currents generating the extracranially measured electrical gradient. Sources of slow wave modulation were located in occipital and posterior parietal cortex, with a right-hemispheric dominance.

A visual Simon task was used to study the influence of aging on visuospatial attention and inhibitory control processes. Responses were much slower for elderly than for young participants. The delay in trials in which stimulus and response side did not correspond as compared to when they did correspond (the Simon effect) was larger for older people, even after correcting for general slowing due to aging. The slowing of responses reflected a slowing of internal processing, as indicated by progressively larger delays of the peak latencies of the N1, the posterior contralateral negativity (PCN), and P3. A comparison between the amplitudes of the PCN and early lateralized readiness potential (pre-LRP) indicated that transmission from posterior sites (PCN) to the motor cortex may be affected by age. The data support the view that aging affects an inhibitory process that controls direct visuomotor transmission.

The present study evaluated the ability of a weak electrical prepulse to modify startle caused by a more intense shock. Painful electrical shocks (150 V, 0.5 ms duration) were presented to the upper arm of college student participants, preceded on some trials by a weaker shock (0.5 ms duration, at perceptual threshold) at the same location. Intense shocks elicited eyeblink reflexes, and these eyeblinks were inhibited by weak electrical prepulses. These data suggest that the inclusion of prepulses immediately preceding painful therapeutic shocks, such as those generated by an implanted cardioverter-defibrillator, might be capable of reducing the startle response generated by that therapeutic shock.

This report evaluated (a) the temporal stability of hemodynamic responses to three tasks using impedance cardiography, and (b) the influence of aging on stress responses in a multi-ethnic pediatric sample. One hundred children 8 to 10 years old and 49 adolescents 15 to 17 years old were tested at study entry and on average 3 years later. Results showed that the composite task-induced changes in stroke volume (SV), cardiac output (CO), total peripheral resistance (TPR), and pre-ejection period (PEP) were moderately stable across 3 years (rs = .36 to .51), with children showing greater stability in task-induced CO change than did adolescents. However, the magnitude of the participant's stress responses changed over time, varied by task, age group, and gender. These results suggest that hemodynamic responses to stress change with aging during childhood and adolescence and that they can be measured reliably.

Differential aversive Pavlovian conditioning with a foul odor as unconditioned stimulus (US) and neutral faces as conditioned stimuli (CS) was compared between 9 noncriminal psychopaths as defined by the Hare Psychopathy Checklist Revised and 12 healthy controls. Event-related potentials (ERP), heart rate, skin conductance response, corrugator EMG, and startle response potentiation as well as valence, arousal, and contingency of the CS were assessed. Whereas the healthy controls (HC) showed significant CS+/CS− differentiation, the psychopaths (PP) failed to exhibit a conditioned response although unconditioned responses were comparable between the groups. N100, P200, and P300 to the CSs revealed that psychopaths were not deficient in information processing and showed even better anticipatory responding than the HC group indicated by the terminal contingent negative variation (tCNV), that lacked, however, CS+ and CS− differentiation. These data indicate a deficit in association formation in psychopaths that may be related to deficient interaction of limbic-subcortical and cortical structures.

An emotion-modulated acoustic startle paradigm for inducing positive and negative affect was used to address pregoal and postgoal affect. Participants played a computerized lottery task in which they chose digits that could match a subsequently displayed, random set of numbers. In the positive conditions, matches led to monetary rewards. In the negative condition, matches led to an aversive noise blast. In three experiments, we found eyeblink startle magnitude was potentiated just prior to feedback concerning reward outcome, suppressed following the feedback that a monetary reward was won, and potentiated when threatened with an aversive noise. When presented with a 0%, 45%, 90%, or 100% chance of winning, higher probabilities suppressed startle response after feedback whereas the 45% trials did not. These data indicate that postgoal positive affect (winning reward) reliably suppressed the startle response whereas pregoal positive affect did not.

Two experiments addressed the following issues concerning modulation of the acoustic startle reflex during emotional imagery: (1) Is startle inhibited or potentiated during imagery of pleasurable events? (2) Does startle modulation differ for personal versus standard imagery scenes? (3) Is startle modulated differently during anger versus fear? For standard scenes, startle was greater during aversive than pleasant imagery, with both exceeding neutral. Blink potentiation was greater during imagery of personal pleasant than nonpersonal pleasant scenes. Startle potentiation did not differ for anger versus fear material, but differences were found in self-report, corrugator EMG, and HR response. These results suggest that in addition to the emotional valence of imagined material, startle reactivity is influenced by the degree of engagement or active disengagement from the sensory environment. The findings also indicate that fear and anger are differentiable in terms of affective report, cardiac mobilization, and expressive behavior, but not at the primary motivational level at which reflex priming occurs.

P300 event-related brain potential (ERP) measures are affected by target stimulus probability, the number of nontargets preceding the target in the stimulus sequence structure, and interstimulus interval (ISI). Each of these factors contributes to the target-to-target interval (TTI), which also has been found to affect P300. The present study employed a variant of the oddball paradigm and manipulated the number of preceding nontarget stimuli (0, 1, 2, 3) and ISI (1, 2, 4 s) in order to systematically assess TTI effects on P300 values from auditory and visual stimuli. Number of preceding nontargets generally produced stronger effects than ISI in a manner suggesting that TTI determined P300 measures: Amplitude increased as TTI increased for both auditory and visual stimulus conditions, whereas latency tended to decrease with increased TTI. The finding that TTI is a critical determinant of P300 responsivity is discussed within a resource allocation theoretical framework.

Both the amplitude and latency of P300 vary with changes in stimulus parameters. Stimuli at intensities or pitch separations near threshold evoke a smaller and later P300. P300 is also affected by extraneous stimulus parameters in tasks where stimulus frequency separation is large and stimuli are well above intensity thresholds. For example, the presence of background white noise when tones are suprathreshold and easily detectable has been reported to increase P300 latency. However, the effects of background masking noise on P300 amplitude and scalp topography have not been reported. Subjects performed an oddball task both in the presence and in the absence of background noise. Performance accuracy was unaffected by background noise. P300 showed latency increases when noise was present, but P300 peak amplitude was unaffected. P300 scalp topography was stable across both conditions. P300 latency is affected by background noise, even when performance is not, but amplitude and amplitude topography remain unaffected.

To examine gender differences in immune reactions to stress and relationships between immune and cardiovascular reactivity, measures of cellular and mucosal immunity and cardiovascular activity were recorded in 77 men and 78 women at rest and in response to active (mental arithmetic) and passive (cold pressor) stress tasks. Both tasks reduced CD4+ T cells and the CD4/8 ratio. Total lymphocytes, NK cells, CD8+ T cells, and secretory immunoglobulin A (sIgA) increased with active stress. Passive stress decreased sIgA. At rest, men had more NK cells, less CD4+ T cells, and fewer neutrophils than women. Mental stress increased sIgA in men but not women. Cardiovascular reactivity to active stress was associated with increases in NK cells. The data support the hypothesis that stress-related increases in lymphocytes are beta-adrenergically mediated, and suggest that the fall in CD4+ T cells may be alpha-adrenergically driven. Mechanisms underlying sIgA reactions are more difficult to determine. Men and women differed in some cell counts, but not in reactivity, although gender influenced sIgA reactions to arithmetic.

Two human Pavlovian conditioning experiments investigated the impact of reinforcement density (the number of reinforced trials divided by the total number of trials) on discrimination learning. Experiment 1 used a negative patterning problem (A+, B+, AB−) and Experiment 2 used a positive patterning problem (A−, B−, AB+). In both experiments, reinforcement density varied across four levels. Response differentiation between reinforced and nonreinforced stimuli was linearly related to the decrease in reinforcement density. Responses to nonreinforced stimuli did not differ between the four groups in either experiment. In contrast to this, responses to reinforced stimuli were considerably more pronounced in conditions with lower reinforcement density. For negative patterning, this replicates and extends similar observations from other species. For positive patterning, this is a finding that has not yet been reported in other experiments. The results are in agreement with the comparator hypothesis (Miller & Matzel, 1988) and with Wagner's (1981) “standard operating procedures” (SOP) model.

Though many studies suggest that fine acoustic details fade from memory after 15 s or even less, everyday experience tells us that the voice of a person or a musical instrument can be recognized long after it was last heard. We wished to determine whether tones leave a lasting memory trace using an experimental model of implicit recognition and testing whether exact pitch information can be retrieved even after 30 s. Event-related brain potentials demonstrated the survival of an accurate representation of tone pitch in the auditory cortex. This result provides a link between short-duration buffering and permanent storage of acoustic information.

Deficits in language comprehension in schizophrenia were examined using event-related potentials (ERPs). Schizophrenic and healthy participants read sentences in which the first clause ended with a homograph, and the second clause started with a target word that was semantically related to the homograph's dominant meaning (e.g., 1. Diving was forbidden from the bridge because the river had rocks in it. or 2. The guests played bridge because the river had rocks in it.). Processing of the targets (e.g., “river”) was expected to be primarily influenced by the preceding overall sentence context (congruent in 1; incongruent in 2) in healthy participants, but to be inappropriately affected by the dominant meaning of homographs (e.g., the “structure” meaning of “bridge”) in sentences like 2 in schizophrenic patients. The N400 ERP component that is known to be sensitive to contextual effects during language processing confirmed these predictions. This showed that language abnormalities in schizophrenia may be related to deficient processing of context-irrelevant semantic representations of words from the discourse.