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Computation of long-distance propagation of impulses elicited by Poisson-process stimulation.

1. The purpose of this work was to determine whether computed temporally coded axonal information generated by Poisson process stimulation were modified during long-distance propagation, as originally suggested by S. A. George. Propagated impulses were computed with the use of the Hodgkin-Huxley equations and cable theory to simulate excitation and current spread in 100-microns-diam unmyelinated axons, whose total length was 8.1 cm (25 lambda) or 101.4 cm (312.5 lambda). Differential equations were solved numerically, with the use of trapezoidal integration over small, constant electrotonic and temporal steps (0.125 lambda and 1.0 microsecond, respectively). 2. Using dual-pulse stimulation, we confirmed that for interstimulus intervals between 5 and 11 ms, the conduction velocity of the second of a short-interval pair of impulses was slower than that of the first impulse. Further, with sufficiently long propagation distance, the second impulse's conduction velocity increased steadily and eventually approached that of the first impulse. This effect caused a spatially varying interspike interval: as propagation proceeded, the interspike interval increased and eventually approached stabilization. 3. With Poisson stimulation, the peak amplitude of propagating action potentials varied with interspike interval durations between 5 and 11 ms. Such amplitude attenuation was caused by the incomplete relaxation of parameters n (macroscopic K-conductance activation) and h (macroscopic Na-conductance inactivation) during the interspike period. 4. The stochastic properties of the impulse train became less Poisson-like with propagation distance. In cases of propagation over 99.4 cm, the impulse trains developed marked periodicities in Interevent Interval Distribution and Expectation Density function because of the axially modulated transformation of interspike intervals. 5. Despite these changes in impulse train parameters, the arithmetic value of the mean interspike interval did not change as a function of propagation distance. This work showed that in theory, whereas the pattern of Poisson-like impulse codes was modified during long-distance propagation, their mean rate was conserved.

Action Potentials↗

Activation sequence and potential distribution maps demonstrating multicentric atrial impulse origin in dogs.

We examined the onset of atrial epicardial excitation by recording unipolar potentials from 360 electrodes arranged in templates affixed to the superior vena cava and right atrium in dogs. Both activation sequence and potential distribution maps were obtained for the period of impulse origin beginning before the surface P wave and continuing through the first 15-20 msec of atrial depolarization. The activation maps demonstrated impulse origin from multiple widely separated sites, resulting in two to three individual wavefronts that merged to form a single widely disseminated wavefront spread over a 50 X 20 mm area by 10-15 msec. Atrial potential maps obtained for the same time periods revealed multiple sites of primary negativity corresponding to the points of impulse origin in the activation maps. The potential distributions and evolution of these maps also indicated the presence of multiple wavefronts originating from widely separated locations, and suggested an extensively dispersed source of impulse origin. One of these sites at the superior cavo-appendicular junction corresponded to the rostral portion of the sinus node and the site of classical unifocal origin. Additional sites of impulse origin and primary negativity distant to the sinus node were noted either concurrently in the same map or in other maps associated with different patterns of impulse initiation. Classical physiological and pharmacological interventions were used to alter adrenergic and cholinergic input to the atrium, and resulted in coincident changes of both the patterns of impulse origin and heart rate. In addition, we examined spontaneous changes in the patterns of impulse initiation which accompanied beat-to-beat changes in cycle length (sinus arrhythmia). There was close agreement between activation and potential maps over the entire steady state and dynamic range of impulse origin. The data can be explained by the concept of a widely distributed system of functionally differentiated but coordinated atrial pacemakers.

Action Potentials↗

Oto-traumatic effects of computer simulated magnetic coil impulse noise: analysis of mechanisms.

The brief impulse noise artifacts of 1.0 ms or less generated by some magnetic coils used in extracranial magnetic stimulation may induce acoustic trauma. We investigated the effects of these magnetic coil acoustic artifacts (MCAA) on the inner ear by exposing rabbits to computer stimulated impulse noise designed to mimic the impulse noise of the coil in spectrum and acoustic energy. The simulated impulse noise stimuli (50 impulses) were varied in maximum peak sound pressure (160, 157, and 155 dB re: 20 muPascal), rise-time (100 microseconds and 1,000 microseconds) and duration. The frequency spectrum of the simulated impulse noises were kept constant at 0.5 kHz to 7 kHz with peak energy in the 2-5 kHz range. The results indicated that the simulated magnetic coil impulse noise caused extensive cochlear damage and permanent threshold shifts largely equal to those induced by the MCAA. The MCAA created slightly greater PTS than the simulated impulse of the same peak sound pressure. Each of the 3 experimental stimuli induced similar PTS in the auditory range of 0.5 to 16 kHz, with the higher peak sound pressure stimuli (157 and 160 dB) causing greatest hearing loss. Increasing the rise-time of the simulated brief impulse noise from 100 microseconds to 1,000 microseconds did not reduce the level of PTS significantly. The results suggest that for brief acoustic signals of around 1 ms or less, the peak pressure and spectral content rather than the rise-time and duration were the important factors in the development of noise-induced hearing loss.(ABSTRACT TRUNCATED AT 250 WORDS)

Acoustic Stimulation↗

[Nerve impulse in the 19th century: it's nature and the method of research].

We demonstrate in this paper how scientists in the 19th century did researches on the nervous system; some scientists tried to make the nature of "nerve impulse" clear only to fail, while others chose to investigate how the nervous system works, leaving the nature of the impulse unknown. A. Mosso and H. D. Rolleston, for example, attempted to detect heat produced in nerves with a view to elucidating the nature of the impulse. The heat, they believed, would suggest that "nerve impulse" was nothing but "a wave of chemical reaction" or "a wave of molecular vibration." On the other hand, C. S. Sherrington who introduced the term synapsis in 1897 to refer to the special connection between nerve cells--special in the sense it offers an opportunity for "nerve impulse" to change in its nature--refrained from examining the nature of the impulse. He believed that it was impossible for science at the time to elucidate the nature. He, therefore, focused his attention to reactions of muscles in an animal caused when various stimulations were applied on animal's skin in a remote area from the muscles. He did not probe into the working of the nerves running between the part where stimulation was given and the part where corresponding reaction occurred. He pursued his studies by using phenomenalistic approach. We call his approach "phenomenalistic" because his research focused only on contradictions of muscles easily seen without probing into minute arrangement in a body. Gotch and Horsley, like Sherrington, did not argue about the nature of "nerve impulse." But unlike Sherrington, they made experiments with electrical changes produced in nerves or a spinal cord, based on the idea that "nerve impulse" should accompany certain electrical changes. Making use of their electrical method effectively, they obtained a series of quantitative data as to the electrical changes. The data they collected allowed them to explore distribution of nerves deep in a body and even led them to contemplate the existence of "field of conjunction" in a spinal cord. They introduced the concept to explain decrease in quantity and delay in transmission time of the electrical change, which was observed when a nerve impulse traversed a certain part of the spinal cord. This idea was considerably similar to "synapse" introduced six years later by Sherrington.

History, 19th Century↗

[The frequency spectrum in the interaction between continuous and impulse noise: an anatomic functional evaluation].

In industrial setting impulse noise rarely occurs in isolation. Impulses are more often superimposed on a background of continuous noise. Since measurement of peak sound pressure level or energy considerations may not provide a sufficient index of danger to hearing, examining the frequency spectra of the noises appeared to be important. Seven groups of five chinchillas were used in this study. Four groups were exposed to octave bands of noise centered at 0.5, 2 or 4 kHz having intensities of 95, 90 and 86 dB SPL respectively or impulse noise of 113 dB peak SPL applied on time per 1 second. Three groups were exposed to the combination of impulse noise and one of the above continuous noises. Each exposure lasted five days. PTS was calculated on each animal using auditory evoked potentials. The cochleas were dissected and evaluated using conventional histological surface preparation and examined with scanning electron microscopy (SEM) employing a JEOL 35 microscope. The groups exposed to only the impulse or to continuous noise alone developed neither PTS nor hair cell loss. Considerable values of PTS and sensory cell loss were observed in animals exposed to impulse noise in combination with 2 and 4 kHz of continuous noise. This interaction effect increases as the spectral overlapping between the impulse and continuous noise increases. In these animals excellent information concerning the sensory cell losses or cell damage was obtained with SEM. The results of the present study demonstrate that interaction between impulse and continuous noise can indicate increased hazard, which is highly dependent not only upon the total energy of the complex exposure but also on the degree of spectral overlapping between impulse and continuous noise.

Animals↗

Impulsivity.

Disorders characterized by impulsivity include disorders of impulse control (intermittent explosive disorder, pyromania, kleptomania, pathological gambling and trichotillomania), paraphilias, sexual impulsions and sexual addictions and impulsive aggression personality disorders (borderline, antisocial, histrionic and narcissistic personality disorders). Impulsivity has a substantial impact on both individuals and society. Impulse control disorders may be conceptualized as a subset of the obsessive-compulsive spectrum. In this article, we examine the genetic and neurobiological aetiology of these disorders and possible treatment options. The link between serotonergic dysfunction and the pathophysiology of impulsivity is discussed, and studies that examine the efficacy of various selective serotonin reuptake inhibitors and other alternatives in the treatment of impulsive disorders such as pathological gambling, sexual addictions and borderline personality disorder are presented.

Disruptive, Impulse Control, and Conduct Disorders↗

Impulsive behaviors in bulimic patients: relation to general psychopathology.

OBJECTIVE: At a general level, impulsivity is related to both bulimic and general psychopathology. However, it is a complex construct, and the specific role of different forms of impulsivity in psychopathology remains to be determined. The present study of bulimic outpatients examined the association of internally and externally directed impulsive behaviors with general and bulimic psychopathology. METHODS: Thirty female bulimic outpatients completed standardized measures of bulimic attitudes/behaviors, general psychopathology and impulsive behaviors. RESULTS: While general psychopathology was associated with internally directed impulsive behaviors (e.g., self-harm), bulimic pathology was more specifically linked with externally directed impulsivity (e.g., theft; reckless driving). DISCUSSION: The results indicate that the bulimia-impulsivity link in eating disordered patients is not simply a by-product of the broader association of impulsivity with psychopathology. Therefore, bulimic pathology does not seem to be just a manifestation of general psychological disturbance. Further research is suggested to test these results and potential clinical implications are outlined.

Adult↗

Varieties of impulsivity.

The concept of impulsivity covers a wide range of "actions that are poorly conceived, prematurely expressed, unduly risky, or inappropriate to the situation and that often result in undesirable outcomes". As such it plays an important role in normal behaviour, as well as, in a pathological form, in many kinds of mental illness such as mania, personality disorders, substance abuse disorders and attention deficit/hyperactivity disorder. Although evidence from psychological studies of human personality suggests that impulsivity may be made up of several independent factors, this has not made a major impact on biological studies of impulsivity. This may be because there is little unanimity as to which these factors are. The present review summarises evidence for varieties of impulsivity from several different areas of research: human psychology, psychiatry and animal behaviour. Recently, a series of psychopharmacological studies has been carried out by the present author and colleagues using methods proposed to measure selectively different aspects of impulsivity. The results of these studies suggest that several neurochemical mechanisms can influence impulsivity, and that impulsive behaviour has no unique neurobiological basis. Consideration of impulsivity as the result of several different, independent factors which interact to modulate behaviour may provide better insight into the pathology than current hypotheses based on serotonergic underactivity.

Animals↗

Elevated impulsivity and impaired decision-making cognition in heavy users of MDMA ("Ecstasy").

RATIONALE: In animal studies, the common club drug 3,4-methylendioxymethamphetamine (MDMA, "Ecstasy") consistently caused a prolonged loss of presynaptic serotonergic neurons, and evidence suggests that MDMA consumption may also affect the human serotonergic system. Serotonin (5-HT) has been implicated in the regulation of impulsivity and such executive functions as decision-making cognition. In fact, MDMA users have shown elevated impulsivity in two studies, but little is known about decision making in drug-free MDMA consumers. OBJECTIVE: The aim of this study was to examine the cognitive neurotoxicity of MDMA with regard to behavioral impulsivity and decision-making cognition. METHODS: Nineteen male, abstinent, heavy MDMA users; 19 male, abstinent cannabis users; and 19 male, drug-naïve controls were examined with the Matching Familiar Figures Test (MFFT) as well as with a Go/No-Go Task (GNG) for impulsivity and with a Gambling Task (GT) for executive functioning. RESULTS: MDMA users showed significantly elevated impulsivity in the MFFT Impulsivity score (I-score), but not in commission errors of the GNG, compared with controls. Cannabis users did not yield altered impulsivity compared with controls. In the GT, MDMA users performed significantly worse than cannabis consumers and controls, whereas cannabis users exhibited the same decision-making capacity as controls. In addition, the I-score as well as the decision-making performance was correlated with measures of MDMA intake. The I-score and the decision-making performance were also correlated. CONCLUSION: These results suggest that heavy use of MDMA may elevate behavioral impulsivity and impair decision-making cognition possibly mediated by a selective impairment of the 5-HT system.

Adult↗

Effects of chronic paroxetine administration on measures of aggressive and impulsive responses of adult males with a history of conduct disorder.

RATIONALE: The role of serotonin in human aggression and impulsivity was evaluated by administering paroxetine or placebo for 3 weeks and comparing the effects on laboratory measures of aggression and impulsivity among male subjects with a history of conduct disorder. METHODS: Twelve male subjects with a history of criminal behavior participated in experimental sessions, which measured aggressive and impulsive responses. Six subjects were assigned to placebo treatment and six subjects to placebo and paroxetine treatment. Aggression was measured using the point subtraction aggression paradigm (PSAP), which provides subjects with an aggressive and monetary reinforced response options. Impulsive responses were measured using a paradigm that gives subjects choices between small rewards after short delays versus larger rewards after longer delays. RESULTS: Chronic administration of paroxetine (20 mg/day) for 21 days produced significant decreases in impulsive responses. Decreases in aggressive responses were evident only at the end of paroxetine treatment. Decreases in impulsive and aggressive responses could not be attributed to a non-specific sedative action because monetary reinforced responses were not decreased as has been observed following CNS sedation. CONCLUSIONS: Inhibition of serotonin reuptake by paroxetine is the possible mechanism for reductions in aggressive and impulsive responses. These results support other data linking serotonin function and aggression and impulsivity.

Administration, Oral↗

Impulsivity, aggression, and neuroendocrine responses to serotonergic stimulation in substance abusers.

Alterations in the activity of central serotonergic systems have been implicated in impulsive and aggressive behavior. We examined the neuroendocrine and psychological responses of 24 substance users with differing levels of aggressiveness and impulsivity to the oral administration of an indirect serotonin agonist fenfluramine (60 mg) or placebo given in a double-blind crossover design. All subjects were volunteers on a closed research ward and were abstinent from drugs for a minimum of 5 days. Baseline plasma prolactin (PRL) levels were greater in the groups with higher levels of self-reported aggressiveness and impulsivity. When adjusted for the baseline, PRL and cortisol responses 180 min after fenfluramine administration were significantly elevated in subjects with higher levels of aggressiveness and impulsivity. Peak cortisol levels were correlated with impulsivity. PRL and cortisol responses to fenfluramine were more strongly correlated with impulsivity than aggressiveness. Also, the more impulsive subjects reported a decrease in subjective states of depression, hostility and anxiety after drug treatment. These data further support the hypothesis of altered serotonergic activity in aggressive and impulsive behaviors.

Adult↗

Subjective self-control and behavioural impulsivity coexist in anorexia nervosa.

OBJECTIVE: Anorexia nervosa (AN) has been associated with impulse regulation problems. This study investigated subjective and behavioural impulsivity in women with anorexia nervosa (n=15) and a control group (n=16). METHOD: A self-report measure (the impulsiveness, venturesomeness, and empathy questionnaire; I(7)) and two behavioural measures (a continuous performance task [CPT]; and a novel risk taking measure [Bets 16]) of impulsivity were used along with the Beck Depression Inventory (BDI). RESULTS: The AN group had elevated BDI scores and lower self-reported impulsiveness and venturesomeness scores, but they also displayed impulsive behaviour on the CPT (more errors of commission with faster reaction times). DISCUSSION: The coexistence, in AN, of self-reported self-control and behavioural impulsivity indicates that the relationship between impulsivity and disordered eating in AN is more complex than previously recognised and supports the view that self-awareness in AN is low.

Adult↗

Impulsivity in youth predicts early age-related cognitive deficits in rats.

Impulsivity is a feature of psychiatric disorders such as mania, addictive behaviors or attention deficit-hyperactivity disorder (ADHD), which has recently been related to complaints of forgetfulness in adults. We investigated whether impulsiveness exerts a long-term influence on cognitive function in rats in a longitudinal study. Impulsivity, assessed by the ability to complete a sequence of presses to obtain food (conditioning box), spatial working memory (8-arm radial maze) assessed with varying degree of attentional load and recognition memory (Y-maze) were tested at different ages. Marked individual differences in impulsivity were observed at youth and remained stable at middle-age despite a general decline in the trait. Working memory scores of impulsive and non-impulsive rats did not differ in youth, whereas by middle-age the impulsive group had impaired working memory and was more sensitive to a higher attentional demand. Thus, impulsiveness in youth predicts cognitive performance in middle-age. These findings may help refine the search for early biological substrates of successful aging and for preventive follow-up of subjects at risk of impaired cognitive aging.

Age Factors↗

Orbitofrontal correlates of aggression and impulsivity in psychiatric patients.

The association between orbital frontal cortex (OFC) volume and aggression and impulsivity was investigated among a heterogeneous group of non-psychotic psychiatric clients. Fifteen non-psychotic subjects from two different psychiatric clinics (New England Medical Center and Lemuel Shattuck Hospital) with a variety of diagnoses were sequentially referred for magnetic resonance imaging (MRI) for clinical purposes. This convenience sample, clinically stable at the time of evaluation, received a standardized psychiatric diagnostic interview, aggression and impulsivity psychometrics (Barratt Impulsivity, Lifetime History of Aggression, and Buss-Perry Aggression scales), and an MRI protocol with image analysis. OFC gray matter volume, total as well as left and right, was significantly and positively associated with motor impulsivity. OFC asymmetry was associated with aggression, though total, left, and right OFC volume measurements were not. For subjects without affective disorder, there was a strong and positive association of the OFC to motor and no-planning subscales of the Barratt Impulsivity Scale. For subjects with affective disorder, there was a strong association of OFC asymmetry to both of the aggression psychometrics. Consistent with expectation, results are suggestive of OFC involvement in the neural circuitry of impulsivity and aggression. The findings suggest a dissociation of the role of the OFC in relation to aggression and impulsivity, such that the OFC may play a part in the regulation of aggressive behavior and a generative role in impulsive behavior.

Adult↗

Neuropsychological and cognitive psychophysiological substrates of impulsive aggression.

The purpose of this study was to test whether subjects who commit impulsive vs non-impulsive aggression differ on measurements of personality, neuropsychology, and cognitive psychophysiology, and whether these differences can yield information regarding the etiology of impulsive aggression. Subjects were two groups of prison inmates, distinguished by their committal of impulsive or nonimpulsive aggression, and matched noninmate controls. All inmates met DSM III-R criteria for an antisocial personality disorder but for no other disorder. Impulsiveness, anger, and peak P300 latencies did not differ between the inmate groups, but verbal symbol decoding and peak P300 amplitudes did. Impulsiveness and verbal skills were inversely correlated. Impulsiveness was inversely correlated with, and verbal skills positively correlated with P300 amplitudes. The results indicate that aggression is not homogenous, even among antisocial persons, and that impulsive aggression is related to neuropsychological and cognitive psychophysiological measures of information processing beyond those factors related to criminality alone.

Adult↗

Impulsivity and phase of illness in bipolar disorder.

BACKGROUND: Impulsivity is prominent in bipolar disorder, but there is little quantitative information relating it to phase of illness. METHODS: We measured impulsivity in patients with bipolar disorder who had not met episode criteria for at least 6 months, patients who were manic, and healthy control subjects. Impulsivity was measured using the Barratt Impulsiveness Scale (BIS) and performance on the computerized Immediate Memory-Remote Memory Task (IMT-DMT), based on the Continuous Performance Test, which has been shown to reflect risk of impulsivity in other populations. RESULTS: BIS scores in euthymic and manic bipolar subjects were identical, and were significantly elevated compared to controls. Commission errors (impulsive responses) on the IMT-DMT were elevated in manic subjects but were identical to controls in euthymic subjects. Measures of impulsivity did not appear related to depressive symptoms. LIMITATIONS: The number of subjects was too small for detailed investigation of the role of comorbidities; subjects were receiving pharmacological treatments. CONCLUSIONS: Impulsivity has state- and trait-related aspects in bipolar disorder.

Adult↗

Impulsivity: a relevant dimension in depression regarding suicide attempts?

BACKGROUND: This study focuses on clinical impulsivity in depressed patients, regarding suicide attempts. METHODS: Fifty depressed in-patients were assessed for impulsivity with the Impulsivity Rating Scale and the Baratt Impulsivity Scale, at admission (W0) and after 4 weeks of treatment (W4), with special attention to suicide attempts. RESULTS: In the whole sample, impulsivity scores decreased significantly between W0 and W4. The scale and the questionnaire correlated slightly with each other, suggesting some differences in impulsivity assessment between patients and clinicians. The two subgroups of patients, suicide attempters (SA) (n = 16) and non-suicide attempters (NSA) (n = 34), were different neither in terms of sample characteristics and antidepressant treatments nor in terms of depression and general psychopathology assessments. However, SA patients scored higher on the impulsivity scale and questionnaire than NSA patients, both at W0 and W4. These results suggest first that impulsivity may be both a trait and a state in depressed suicide attempters and second that it may be relevant in terms of suicide attempts in depression.

Adult↗

Impulsivity, gender, and response to fenfluramine challenge in borderline personality disorder.

Behavioral impulsivity in borderline personality disorder (BPD) is associated with indices of diminished central serotonergic function, independent of suicidal behavior, depression or alcohol use disorder. Many of these studies have been conducted among males in specialized settings. Studies of BPD females, who constitute the majority of BPD patients, are generally conducted in community settings and report inconsistent findings. We studied gender differences in behavioral impulsivity and the prolactin response to D,L-fenfluramine (FEN) in BPD subjects in a community setting. A FEN challenge study was conducted with 64 BPD subjects (20 male, 44 female), and 57 controls (36 male, 21 female). Axis I and II disorders, including BPD, and suicidal histories were assessed by structured interviews. Controls were free of Axis I and II disorders. Impulsivity and aggression were assessed by the Buss-Durkee Hostility Inventory, Barratt Impulsiveness Scale, Minnesota Multiphasic Personality Inventory-Psychopathic Deviate subscale, and the Brown-Goodwin Lifetime History of Aggression. Male, but not female, BPD subjects had significantly diminished prolactin responses compared to controls. Impulsivity and aggression each predicted prolactin responses. A significant effect of BPD diagnosis on prolactin response was eliminated when impulsivity was co-varied. Impulsivity and aggression were inversely related to delta-prolactin and peak-prolactin responses among male but not female subjects. Gender differences in central serotonergic function may contribute to variations in impulsivity in BPD.

Adult↗