Prestimulus effects on startle magnitude: Sensory or motor?

Startle may be inhibited when the startling event is preceded by a stimulus; this is called prepulse inhibition (PPI) when the prestimulus is weak and nonstartling (s) and paired pulse inhibition when the prestimulus elicits startle (S1). The authors examined the relationship of these measures across species and tested whether paired pulse inhibition-like PPI-is independent of the startling effects of the prestimulus. PPI (s-S1 configuration) and paired pulse inhibition (S1-S2 configuration) were elicited in 1 test, using similar stimulus parameters in rats and humans. The amount of PPI and paired pulse inhibition was significantly correlated within subjects in both rats and humans. Paired pulse inhibition was not diminished when the startling effects of S1 were eliminated by a weak prepulse (s-S1-S2 configuration), nor was it enhanced when these prepulse effects were eliminated by the dopamine agonist apomorphine (in rats). Despite apparent differences in the inhibitory processes mediating PPI and paired pulse inhibition, both are independent of the motoric response to the prestimulus. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Human fetal heart rate dishabituation between thirty and thirty-two weeks gestation

Few studies of human fetal habituation have included dishabituation procedures (i.e., assessment of the reemergence of a habituated response) to determine if response decrements are the result of reevaluation of information (a brain process) or fatigue of peripheral receptors. The purpose of this study is to describe the ability of the human fetus to learn and recall information with procedures to assess the central nervous system. Fetal heart rate (FHR) of 84 fetuses between 30 and 32 weeks gestational age was examined in response to 3 series of vibroacoustic (VA) stimuli presented at pseudorandom intervals of 25-45 s over the head of the fetus. Responses to the first series of 15 stimuli (S1) were compared with an identical second series of 15 stimuli (S1) presented over the head of the fetus. Between the 2 series, a novel (dishabituating) VA stimulus (S2) was presented, differing from S1 in intensity and frequency. The third series of S1s was applied to the mother's thigh as a control for possible maternal responses to the stimulus. Prestimulus FHR was computed during a 5 s interval before each stimulus, and mean FHR was computed during the intertrial interval (average FHR). The response to S1 during the first series of trials (1-15) produced a sustained rise in both prestimulus and average FHR, r(83) = .90, p < .001. After the novel S2 (trial 16) the rate of change was attenuated for average FHR, r(83) = .12, ns, to S1 for trials 17-31 but not prestimulus FHR, r(83) = .50, p < .001. The decrease in FHR response was reestablished when stimulation was applied to mother's thigh, trials 32-41, r(83) = .92, p < .001. A significant habituation pattern across trials was observed for the first series of S1s when prestimulus HR was subtracted from each preceding average FHR value (delta FHR). After the single novel stimulus (S2), the FHR response to S1 reemerged. All combinations of beginning and ending series slopes were compared, and only the rate of change during the last 4 trials of the initial presentation of S1 and the first 4 trials after the novel stimulus was significant, F(1, 82) = 9.21, p < .003. Uterine contractions collected from the continuous record were not related to the presentation of the novel stimulus, chi 2(1, N = 84) = 0.59, p < .50, ns, or delta FHR slope after the novel stimulus, chi 2(9, N = 84) = 10.52, p < .50, ns. These results established that the 32 week human fetus is capable of detecting, habituating, and dishabituating to an external stimulus and support the premise that areas of the human fetal central nervous system critical for detecting and discriminating information and for learning and memory have developed by the early third trimester.     

Inhibition of human eye blink by brief acoustic stimulus.

A corneal air puff (S2) which elicited eye blinks in 10 undergraduates either appeared alone (control) or was preceded by a brief acoustic stimulus (S1) at a variety of temporal intervals (50-2,020 msec). Amplitude of the eye-blink response to S2 was depressed by S1 at short intervals as compared with control trials; peak inhibition appeared at about 70 msec of S1-S2 separation and declined at longer intervals. An intense S1 was more effective than a weak S1 at short intervals. Inhibition was independent of prior experience with S1 and S2 and of overt responding to S1, and no systematic change in inhibition occurred during testing. The temporal course of inhibition was the same as that previously obtained with the acoustic-startle reflex in rats and the nictitating membrane reflex to circumorbital shock in rabbits. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Change detection model for serially correlated data.

Develops a time series model for detecting change in psychophysiological data from a single S following stimulation. A stationary model is assumed for the periods before stimulation; it is assumed that the S returns to a steady or basal state between stimuli. A 1st-order autoregression (Markov process) is fit to all prestimulus data for a single S. Predictions are then made into the poststimulus regions. If the time series is Gaussian and if there is no response to the stimulus, the differences between 1-step predictions and the corresponding observations are independent and normally distributed with mean zero and constant variance which can be estimated. Statistical tests for change are constructed to determine whether the differences are significant. The objective is to detect any deviations from the stationary structure of the prestimulus periods. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Augmentation of the rat's acoustic startle reflex by nonreflexogenic stimuli.

The size of the rat's acoustic startle reflex was augmented by brief acoustic clicks (which did not themselves elicit startle) presented several milliseconds before the reflex-eliciting stimulus (RS). The same clicks presented after the RS gave relatively weak augmentation that was present in the 1st, but not the 2nd, testing session. Brief footshocks set to 75% of each animal's flinch threshold augmented startle when presented both before and after the RS in both testing sessions. Augmentation by a leading footshock increased with shock intensity and also with the intensity of the RS. Augmentation by a trailing footshock increased with shock intensity and also with the intensity of the RS. Reflex size is not fixed at the time of reflex elicitation but can be augmented by a later nonreflexogenic stimulus. Reflex augmentation may be caused by the 2nd member of a stimulus pair discharging elements of the reflex pathway that were partially activated by the 1st. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Temporal integration of acoustic stimulation obtained in reflex inhibition in rats and humans.

Investigated whether inhibition provided by initial stimuli of various durations conforms to established temporal integration functions. Initial stimuli (S1) were noise bursts varying in duration (2, 20, or 200 msec) and intensity (55 or 85 db). Eliciting stimuli (S2) for 6 Holtzman rats were intense tone bursts, which elicited the acoustic startle reflex, and for 9 19–24 yr old humans were electrotactile stimuli to the forehead, which elicited the eye blink. Findings reveal that inhibition was greater with the 85-db S1 stimulus and increased linearly with log increases in duration. Data suggest that the acoustic substrate for reflex inhibition has a long-time constant. There was one exception to this general finding. For 7 human Ss, inhibition declined when the duration of the 85-db S1 was increased from 20 to 200 msec. Postexperimental questioning and video monitoring suggest that this anomaly resulted from a reflex-enhancing arousal process. (38 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of experience on stimulus-produced reflex inhibition in the rat.

Notes that acoustic-startle behavior in the rat is inhibited by changes in the auditory and visual environment which immediately precede reflex elicitation. A series of 7 experiments was conducted with 165 male Holtzman albino rats which established that this effect was not present in the naive S unless the preliminary stimulus was a relatively intense noise burst. With visual stimuli and moderate auditory stimuli the requisite condition for the production of reflex inhibition was that the S should have experienced the eliciting stimulus. Exposures to the to-be-inhibitory stimulus or to a conjunction of this stimulus and the eliciting stimulus were not necessary. Once established, the inhibitory effect was not degraded by week-long rest periods nor by "unreinforced" exposures to the inhibitory stimulus. It is conjectured that the experiential effect may reflect some increase in a nonspecific state of alertness or arousal. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Emotion, novelty, and the startle reflex: Habituation in humans.

Previous research with both animal and human Ss has shown that startle reflex magnitude is potentiated in an aversive stimulus context, relative to responses elicited in a neutral or appetitive context. In the present experiment, the same pleasant, unpleasant, and neutral picture stimuli were repeatedly presented to human Ss. Startle reflex habituation was assessed in each stimulus context and was compared with the habituation patterns of heart rate, electrodermal, and facial corrugator muscle responses. All systems showed initial differentiation among affective picture contents and general habituation over trials. The startle reflex alone, however, continued to differentiate among pleasant, neutral, and unpleasant pictures throughout the presentation series. These results suggest that (1) the startle probe reflex is relatively uninfluenced by stimulus novelty, (2) the startle modulatory circuit (identified with amygdala-reticular connections in animals) varies systematically with affective valence, and (3) the modulatory influence is less subject to habituation than is the obligatory startle pathway or responses in other somatic and autonomic systems. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Visual function measured by reflex modification in rats with inherited retinal dystrophy.

Two experiments, with 16 Ss, examined developmental changes in visual function in the Royal College of Surgeons (RCS) rat with inherited retinal degeneration (retinal dystrophy) by studying the inhibition of acoustic startle reflexes by visual prestimuli. Compared with a congenic strain of nondystrophic rat, RCS Ss showed an increase in the interstimulus interval between the inhibitory prestimulus and the eliciting stimulus that produced maximal inhibition, a result suggesting a decrease in the speed of processing. The amount of inhibition also decreased over time, which suggests a progressive loss of visual function. Simultaneous presentation of auditory and visual prestimuli was used to demonstrate that the changes in inhibition were related to alterations in visual function and that auditory function was not impaired. Results show that reflex modification is a suitable test for evaluating visual dysfunction in rats. ( 27 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Effects of sequential stimuli on Halobacterium salinarium photobehavior

We analyzed the motor photoresponses of Halobacterium salinarium to different test stimuli applied after a first photophobic response produced by a step-down of red-orange light (prestimulus). We observed that pulses given with a suitable delay after the prestimulus produced unusual responses. Pulses of blue, green, or red-orange light, each eliciting no response when applied alone, produced a secondary photophobic response when applied several seconds after the prestimulus; the same occurred with a negative blue pulse (rapid shut-off and turning on of a blue light). Conversely, no secondary photophobic response was observed when the test stimulus was a step (a step-up for red-orange light, a step-down for blue light) of the same wavelength and intensity. When the delay was varied, different results were obtained with different wavelengths; red-orange pulses were typically effective in producing a secondary photophobic response, even with a delay of 2 s, whereas the response to a blue pulse was suppressed when the test stimulus was applied within 5 s after the prestimulus. The secondary photophobic response to pulses was abolished by reducing the intensity of the prestimulus without affecting the primary photophobic response. These results, some of which were previously reported in the literature as inverse effects, must be produced by a facilitating mechanism depending on the prestimulus itself, the occurrence of reversals being per se ineffective. The fact that red-orange test stimuli are facilitated even at the shortest delay, whereas those of different wavelengths become effective only after several seconds, suggests that the putative mechanism of the facilitating effect is specific for different signaling pathways.     

Facilitation and inhibition of the human startle blink reflexes by stimulus anticipation.

The cutaneous eyeblink has 2 electromyographic components, 1 unilateral and early (R1) and 1 bilateral and late (R2), which are served by different neural pathways. These 2 reactions were measured when the eliciting stimulus was expected or relatively surprising. Forewarning was varied in 3 ways: Subjects received notice that the stimulus was about to occur on some trials (Experiment 1); delivered the stimulus to themselves on some trials (Experiments 2 & 3); or experienced a series of trials in which a tone was paired with the eliciting stimulus, followed by tone-alone trials interspersed with test trials (Experiment 4). In each case, forewarning enhanced R1 amplitudes while depressing R2 but reduced the latency of both components. This mixed pattern of effects reveals that the preparatory state provoked by forewarning focuses excitatory and inhibitory processes simultaneously on different reflex pathways: inhibition central and excitation peripheral. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Event-related potentials during an auditory discrimination with prepulse inhibition in patients with schizophrenia, obsessive-compulsive disorder and healthy subjects

Prepulse inhibition (PPI) is a measure of the influence of a stimulus (S1) on the response elicited by a second stimulus (S2) occurring shortly afterwards. Most S1/S2 measures of gating have used behavioural startle and the P50 event-related potential (ERP) amplitudes to detect PPI in a simple paired stimulus paradigm. We report on two behavioural (reaction time, RT, and the electromyographically recorded response of the musculus orbicularis oculi, EMG) and 5 ERP measures of PPI where S2 was the target in an auditory two-tone discrimination. Subjects were 21 healthy controls (CON), 11 obsessive-compulsive (OCD) and 9 schizophrenic patients (SCH). The prepulse 100 ms before S2 induced more omission errors and longer RTs compared to 500ms S1-S2 interval in all subjects. PPI was also evident in EMG, P50, N1, P3 but not P2 or N2 amplitudes of CON subjects. SCH patients showed attenuation of PPI on the same measures. OCD patients were characterized only by their slow RT and a marginal attenuation of PPI of the EMG response. A correlational analysis implied separate relationships of ERP indices of PPI to the cognitive and psychomotor consequences of the prepulse on behavioural and discrimination responses. However, SCH patients showed a general rather than a specific impairment of these indices.     

A parametric study of the N40 auditory evoked response in rats

BACKGROUND: The N40 auditory evoked potential (EP) in rats is used to study "sensory gating." Our first goal was to compare the effects of systematically varying the characteristics of the pairs of clicks (S1-S2), on the degree of attenuation of the responses to S2 stimuli. A second goal was to examine the effects of changing S2 stimuli on the degree of attenuation of the responses to the deviant stimulus. METHODS: The N40 EP was recorded from 10 rats in eight identical-pair conditions and from 11 rats in two paradigms: nonidentical pairs and short trains of identical stimuli followed by a deviant stimulus. RESULTS: In eight identical-pair conditions changing stimulus duration, intensity, or frequency had no effect on the degree of attenuation of S2 responses. Changing S2 stimulus or presenting a deviant stimulus following a train of identical stimuli had a significant effect on the degree of attenuation of the response to the deviant stimulus. CONCLUSIONS: We conclude that the rat N40 EP is sensitive to stimulus change and can contribute to the study of both habituation and dishabituation mechanisms of "sensory gating."     

Stimulus quality affects expression of the acoustic startle response and prepulse inhibition in mice.

The relationship between stimulus intensity and startle response magnitude (SIRM) can assess the startle reflex and prepulse inhibition (PPI) with advantages over more commonly used methods. The current study used the SIRM relationships in mice to determine differences between white noise and pure tone (5 kHz) stimuli. Similarly to rats, the SIRM relationship showed a sigmoid pattern. The SIRM-derived reflex capacity (RMAX) and response efficacy (slope) of the white noise and pure tone stimuli in the absence of prepulses were equivalent. However, the pure tone startle response threshold (DMIN) was increased whereas the stimulus potency (1/ES??) was decreased when compared to white noise. Prepulses of both stimulus types inhibited RMAX and increased DMIN, but the white noise prepulses were more effective. Both stimulus intensity gating and motor capacity gating processes are shown to occur, dependent on prepulse intensity and stimulus onset asynchrony. Prepulse intensities greater than 10 dB below the startle threshold appear to produce PPI via stimulus intensity gating, whereas a motor capacity gating component appears at prepulse intensities near to the startle threshold. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Taking a bright view of negative priming in the light of dim stimuli: Further evidence for memory confusion during episodic retrieval.

A same–different letter-matching task was used to examine the effects of stimulus intensity on negative priming, which is poorer performance when target letters have been presented as distractor letters on the immediately preceding trial. In Exp 1, with 68 college students, stimulus intensity was manipulated between-participants, whereas in Exp 2, with 32 college students, it varied randomly from trial-to-trial within-participants. In Exp 1, negative priming was equivalent for both stimulus intensities. In Exp 2, negative priming effects were larger for repeated intensity stimuli than for nonrepeated intensity stimuli, when stimulus intensity was dim. Furthermore, for repeated intensity stimuli, negative priming effects were enhanced when the overt response required to the stimulus was repeated from prime to probe trial. These results are consistent with the hypothesis that negative priming may be due to memory confusion, rather than to inhibition of the distractor stimuli. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Intentional and Unintentional Contributions to Nonspecific Preparation: Electrophysiological Evidence.

The authors hypothesized that there are distinct intentional and unintentional influences on nonspecific preparation for a future event. In 2 experiments, participants responded to an imperative stimulus (S?) that was presented equiprobably either 400 ms or 1,200 ms after the offset of a warning stimulus (S?). During the S?-S? interval, the authors measured the contingent negative variation (CNV), an event-related brain potential reflecting nonspecific preparation. S? provided either no information or reliable information about the duration of the impending S?-S? interval, thereby allowing an intentional influence on the state of preparation. The effect of S? information on the CNV was approximately additive to the effect of the S?-S? interval that was used on the preceding trial. This supports the view that the preceding S?-S? interval contributes unintentionally to the state of nonspecific preparation guided by a process of trace conditioning. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Sensitive and rapid bioassay for analysis of P-glycoprotein-inhibiting activity of chemosensitizers in patient serum

The quantitative differences among individuals in the natural reciprocal inhibition of the soleus H-reflex during dorsiflexion were examined, in conjunction with the maximal H-reflex as the test reflex size in each individual. Maximal H-reflex was expressed relative to the maximal M-response (H(max)) when compared among individuals. Analysis showed that with increases in H(max) at rest in each individual, the inhibitory effect was first enhanced, then reached a peak, and was finally alleviated. This pattern was similar to the intraindividual pattern of the inhibitory effect induced by specific conditioning stimulus as a function of the test reflex size.     

An electrophysiological study of the insertion of overt response choice.

Using electrophysiological measures, the authors studied changes in prestimulus state, stimulus identification, and response-related processing when, in a go/no-go task, forced choice between 2 overt go responses was inserted. The authors observed decreased prestimulus motor preparation (electromyogram), no change in stimulus identification time (selection negativity), a minor increase in response selection time (lateralized readiness potential), a large increase in response preparation time (lateralized readiness potential), a minor effect on response execution time (electromyogram), and a decrease in the activation of a response-inhibition process on no-go trials (frontal event-related potential). The existence of the response-inhibition process was verified by the presence of inverted lateralized readiness potentials on no-go trials. Pure insertion of response choice in a task seems impossible because the choice between activation and inhibition (go/no-go) always seems already present. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Nonsustained reentry following successive stimulation of cardiac tissue through a unipolar electrode

INTRODUCTION: Using numerical simulations, we predict that nonsustained reentry occurs following a strong, premature stimulus through a unipolar electrode. METHODS AND RESULTS: Our simulations were based on the bidomain model of cardiac tissue, and the active membrane properties were represented by the Beeler-Reuter model. An outwardly propagating wavefront was excited by an initial stimulus (S1). A second stimulus (S2) was then applied through the same electrode. Nonsustained reentry or reentrant-like behavior followed the S2 stimulus for both cathodal and anodal stimulation, and were associated with "break" stimulation but not with "make" stimulation. The direction of spiral-wave rotation was reversed when the polarity of the stimulus was reversed. These complex dynamics occur only for a narrow window of S1-S2 intervals. During anodal S2 stimulation, two different modes of reentry exist. Our simulations also explain the "no response" phenomenon. CONCLUSION: Our mathematical model predicts that both anodal and cathodal unipolar S2 stimulation results in reentry. This behavior arises from an interaction of virtual anodes and cathodes surrounding the stimulating electrode.