Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Janette L. Smith is active.

Publication


Featured researches published by Janette L. Smith.


The Journal of Physiology | 2006

Motor commands contribute to human position sense

Simon C. Gandevia; Janette L. Smith; Matthew Crawford; U. Proske; Janet L. Taylor

The role of afferent inflow and efferent outflow (or command) signals in judgements of limb position has been debated for over a century. One way to assess this is to check for changes during complete paralysis, with the current view being that perceived movements or position changes do not usually accompany attempts to contract paralysed muscles. To re‐examine this, we asked six naïve subjects to carry out a simple position‐matching task at the wrist. In the absence of vision, subjects accurately perceived the position to which their right wrist had been moved by the experimenter by matching it with their left hand. There was no significant change in perception when position was matched during sustained flexion or extension efforts. Then we paralysed and anaesthetized the right arm with ischaemia in order to produce a ‘phantom’ hand. The perceived position of the wrist changed by more than 20 deg when subjects attempted to flex or extend their hand when it was paralysed and anaesthetized. Further studies showed that this illusion was not dependent on the way in which the paralysis was produced and that the size of the position illusion increased when the level of effort during paralysis increased. These results establish for the first time a definitive role for ‘outflow’ signals in position sense.


Drug and Alcohol Dependence | 2014

Deficits in behavioural inhibition in substance abuse and addiction: A meta-analysis

Janette L. Smith; Richard P. Mattick; Sharna Jamadar; Jaimi M. Iredale

AIMS Deficits in behavioural inhibitory control are attracting increasing attention as a factor behind the development and maintenance of substance dependence. However, evidence for such a deficit is varied in the literature. Here, we synthesised published results to determine whether inhibitory ability is reliably impaired in substance users compared to controls. METHODS The meta-analysis used fixed-effects models to integrate results from 97 studies that compared groups with heavy substance use or addiction-like behaviours with healthy control participants on two experimental paradigms commonly used to assess response inhibition: the Go/NoGo task, and the Stop-Signal Task (SST). The primary measures of interest were commission errors to NoGo stimuli and stop-signal reaction time in the SST. Additionally, we examined omission errors to Go stimuli, and reaction time in both tasks. Because inhibition is more difficult when inhibition is required infrequently, we considered papers with rare and equiprobable NoGo stimuli separately. RESULTS Inhibitory deficits were apparent for heavy use/dependence on cocaine, MDMA, methamphetamine, tobacco, and alcohol (and, to a lesser extent, non-dependent heavy drinkers), and in pathological gamblers. On the other hand, no evidence for an inhibitory deficit was observed for opioids or cannabis, and contradictory evidence was observed for internet addiction. CONCLUSIONS The results are generally consistent with the view that substance use disorders and addiction-like behavioural disorders are associated with impairments in inhibitory control. Implications for treatment of substance use are discussed, along with suggestions for future research arising from the limitations of the extant literature.


Clinical Neurophysiology | 2004

Inhibitory processing during the Go/NoGo task: an ERP analysis of children with attention-deficit/hyperactivity disorder.

Janette L. Smith; Stuart J. Johnstone; Robert J. Barry

OBJECTIVE Previous event-related potential (ERP) research on inhibitory functioning in attention-deficit/hyperactivity disorder (AD/HD) has often failed to use tasks which optimally assess inhibition. We report on an improved measure of inhibitory function, involving inhibition of a prepotent response, in children with AD/HD. METHODS Twelve males with AD/HD and 12 control males, aged 7-12 years, completed a cued Go/NoGo task where Go stimuli were presented on 70% of trials. ERP and behavioural measures were collected, together with reading, spelling and full-scale IQ scores. RESULTS The behavioural performance of children with AD/HD was not significantly different from normal controls, although children with AD/HD made faster responses and more errors. Group differences were apparent in the early processing components (P1, N1, P2) of responses to Warning, Go and NoGo stimuli. For the frontally maximal N2, a NoGo>Go effect was found, consistent with previous work linking this component with inhibitory processing. In control children this effect was particularly strong in the right frontal region, while children with AD/HD showed a much larger NoGo>Go effect, and an earlier N2 peak, than controls, with a focal shift to the left frontal region. CONCLUSIONS Compared with normal controls, children with AD/HD demonstrate early stimulus processing atypicalities, suggesting problems with sensory registration and identification of stimuli. Further, N2 results suggest that children with AD/HD must trigger the inhibition process earlier and more strongly than controls to perform at a comparable behavioural level. SIGNIFICANCE The results support the theory that behavioural inhibition is deficient in AD/HD, as children with AD/HD show abnormalities in inhibitory ERP components relating to the effort involved in inhibiting a prepotent response.


The Journal of Neuroscience | 2006

Fatigue-sensitive afferents inhibit extensor but not flexor motoneurons in humans.

Peter G. Martin; Janette L. Smith; Jane E. Butler; Simon C. Gandevia; Janet L. Taylor

The role of group III and IV muscle afferents in controlling the output from human muscles is poorly understood. We investigated the effects of these afferents from homonymous or antagonist muscles on motoneuron pools innervating extensor and flexor muscles of the elbow. In study 1, subjects (n = 8) performed brief maximal voluntary contractions (MVCs) of elbow extensors before and after a 2 min MVC of the extensors. During MVCs, electromyographic responses from triceps were evoked by stimulation of the corticospinal tracts [cervicomedullary motor evoked potentials (CMEPs)]. The same subjects repeated the protocol, but input from fatigue-sensitive afferents was prolonged after the fatiguing contraction by maintained muscle ischemia. In study 2, CMEPs were evoked in triceps during brief extensor MVCs before and after a 2 min sustained flexor MVC (n = 7) or in biceps during brief flexor MVCs before and after a sustained extensor MVC (n = 7). Again, ischemia was maintained after the sustained contractions. During sustained MVCs of the extensors, CMEPs in triceps decreased by ∼35%. Without muscle ischemia, CMEPs recovered within 15 s, but with maintained ischemia, they remained depressed (by ∼28%; p < 0.001). CMEPs in triceps were also depressed (by ∼20%; p < 0.001) after fatiguing flexor contractions, whereas CMEPs in biceps were facilitated (by ∼25%; p < 0.001) after fatiguing extensor contractions. During fatigue, inputs from group III and IV muscle afferents from homonymous or antagonist muscles depress extensor motoneurons but facilitate flexor motoneurons. The more pronounced inhibitory influence of these afferents on extensors suggests that these muscles may require greater cortical drive to generate force during fatigue.


Journal of Psychophysiology | 2005

Development of Inhibitory Processing During the Go/NoGo Task

Stuart J. Johnstone; Carly B. Pleffer; Robert J. Barry; Adam R. Clarke; Janette L. Smith

Abstract. The aim of the present study was to investigate behavioral and electrophysiological indices of developing response activation and inhibition processes in child, young-adult, and adult groups. Sixty subjects, with 20 in each of the child (mean age 10.8 years), young-adult (mean age 20.7 years), and older adult (mean age 36.4 years) groups, performed an auditory Go/NoGo task while task performance variables and EEG were recorded. ERPs were derived to Go (response activation) and NoGo (response inhibition) stimuli, with the amplitude and latency of the N1, P2, N2, and P3 ERP components analyzed as a function of age. Results indicate improved task performance, and a reduction in the latency of each component and the amplitude of the N2 and P3 components, with increasing age. Analyses of Go versus NoGo effects indicated differential utilization of inhibition-related processing stages in children compared to adults, with some minor differences between the two adult groups. Go/NoGo effects were evident...


Clinical Neurophysiology | 2011

Conflict and inhibition in the cued-Go/NoGo task

William M. Randall; Janette L. Smith

OBJECTIVE Current debate centres on the inhibitory and conflict interpretations of the N2 and P3 components of the event-related potential (ERP). We examined behavioural responses and ERPs in a cued-Go/NoGo task. METHODS Participants were required to inhibit a planned response (NoGo target after Go cue), change a planned response to a different one (Invalid cueing), and activate an unexpected response (Go target after NoGo cue). RESULTS Responses were slower when participants had to change a planned response, and execute an unplanned response. N2 was more negative whenever the presented target required a different response to what was expected based on the cue. In contrast, P3 was increased when participants had to change or inhibit a planned response, but not when executing a response where none was planned. CONCLUSIONS N2 results lend support to the conflict account, while P3 reflects cancellation of a planned response. SIGNIFICANCE This paper provides the first test of conflict involving activation of an unplanned response in a cued-Go/NoGo task.


Cognitive, Affective, & Behavioral Neuroscience | 2009

Anticipatory reconfiguration elicited by fully and partially informative cues that validly predict a switch in task

Frini Karayanidis; Elise Mansfield; Kasey L. Galloway; Janette L. Smith; Alexander Provost; Andrew Heathcote

Task-switching studies show no behavioral benefit of partially informative cues. However, ERP evidence of an early cue-locked positivity elicited by both fully and partially informative cues suggests that both cues trigger an anticipatory component of task set reconfiguration (Nicholson, Karayanidis, Davies, & Michie, 2006). We examined this apparent discrepancy using a cued-trials task-switching paradigm with three tasks. The ERP finding of an early cue-locked positivity was replicated for both switch-to cues, which validly predicted an upcoming switch trial and specified the new task set, and switch-away cues, which validly predicted an upcoming switch trial but not the new task set. This component was not elicited by a noninformative cue that did not specify whether the task would switch or repeat. Switch-away cues resulted in more accurate but not faster responding than did noninformative cues. Modeling of decision processes confirmed a speed-accuracy trade-off between these conditions and a preparation benefit for both switch-to and switch-away cues. These results indicate that both fully and partially informative cues elicit an early anticipatory component of task set reconfiguration that is reflected in the early cue-locked positivity. We argue that the pattern of results is most consistent with a task set inhibition account of this early anticipatory component of task set reconfiguration.


International Journal of Psychophysiology | 2010

Sequence effects support the conflict theory of N2 and P3 in the Go/NoGo task

Janette L. Smith; Elizabeth Smith; Alexander Provost; Andrew Heathcote

In two-choice tasks the preceding sequence of stimuli robustly influences both the P3 ERP component and reaction time (RT) to the current stimulus. We examined sequence effects in both two-choice and Go/NoGo tasks to distinguish between inhibition and conflict accounts of the N2 and P3 components. RT results suggested similar subjective expectancies were generated in the Go/NoGo and two-choice task. N2 was increased for all unexpected stimuli, even when no response inhibition was required, consistent with a conflict interpretation. The Go/NoGo P3 results also suggested a conflict explanation, and that this conflict was reduced if the response had been recently performed. These results support a reconsideration of the roles of N2 and P3 in all inhibition and conflict tasks, and the Go/NoGo task in particular.


International Journal of Psychophysiology | 2013

Motor and non-motor inhibition in the Go/NoGo task: an ERP and fMRI study

Janette L. Smith; Sharna Jamadar; Alexander Provost; Patricia T. Michie

The contribution of movement-related activity to Go/NoGo ERP differences has been debated for 25 years. In this study, we examined ERP and fMRI measures of activity in twenty adults performing non-motor (count) and motor (right-handed button press) trials of the Go/NoGo task. Task performance was highly accurate and similar in the ERP and fMRI environments. No significant task-related effects were observed for the N2 component; however, we observed a substantial increase in positivity for Press NoGo compared to Count NoGo trials. The fMRI results also revealed significant deactivations for Press NoGo relative to Count NoGo trials in several left-lateralised motor-related areas, including the inferior frontal gyrus, precentral gyrus and supplementary motor area. Together, the results indicate that the P3 NoGo>Go effect in motor tasks is caused not by movement-related negativity on Go trials but by inhibition-related positivity on NoGo trials, and that this is associated with deactivation of motor areas involved in the Go response.


Drug and Alcohol Dependence | 2013

Evidence of deficits in behavioural inhibition and performance monitoring in young female heavy drinkers

Janette L. Smith; Richard P. Mattick

BACKGROUND New models of the development and maintenance of substance abuse give increasing importance to the role of deficits in inhibitory function. Much of the evidence to support this claim comes from male participants, despite some researchers showing greater disinhibition in females. Clearly, more research on female heavy drinkers is warranted. In this study, we examine behavioural and psychophysiological measures of inhibitory function in female young adults who do and do not regularly drink heavily. METHODS Participants were thirty female young adults (aged 18-21) who drink heavily (four or more standard drinks per occasion) at least once a month (n=13) or who drink heavily less often than this (n=17); none regularly used any other drugs, including tobacco. They underwent interviews assessing prior use of alcohol, before completing a stop-signal task while brain electrical activity was recorded. RESULTS Regular heavy drinkers displayed a longer stop-signal reaction time (the time required to stop an inappropriate response), and a larger P3 increase for successful compared to failed inhibition trials. Heavy drinkers also displayed a smaller error-related negativity (ERN) amplitude, indexing a deficit in performance monitoring. CONCLUSION These results indicate that large deficits in inhibitory processing and performance monitoring occur in young female heavy drinkers, and that heavy drinkers may have to work harder in order to successfully inhibit a response. Future research may determine whether these deficits pre-date or are caused by alcohol abuse.

Collaboration


Dive into the Janette L. Smith's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Janet L. Taylor

University of New South Wales

View shared research outputs
Top Co-Authors

Avatar

Simon C. Gandevia

University of New South Wales

View shared research outputs
Top Co-Authors

Avatar

Richard P. Mattick

National Drug and Alcohol Research Centre

View shared research outputs
Top Co-Authors

Avatar

Jacqueline A. Rushby

University of New South Wales

View shared research outputs
Top Co-Authors

Avatar

Adam R. Clarke

University of Wollongong

View shared research outputs
Top Co-Authors

Avatar

Peter G. Martin

Prince of Wales Medical Research Institute

View shared research outputs
Top Co-Authors

Avatar

Jane E. Butler

Neuroscience Research Australia

View shared research outputs
Top Co-Authors

Avatar

Jaimi M. Iredale

National Drug and Alcohol Research Centre

View shared research outputs
Researchain Logo
Decentralizing Knowledge