Publications by authors named "Sebastian C Coleman"

The post-movement beta rebound has been studied extensively using magnetoencephalography (MEG) and is reliably modulated by various task parameters as well as illness. Our recent study showed that rebounds, which we generalise as "post-task responses" (PTRs), are a ubiquitous phenomenon in the brain, occurring across the cortex in theta, alpha, and beta bands. Currently, it is unknown whether PTRs following working memory are driven by transient bursts, which are moments of short-lived high amplitude activity, similar to those that drive the post-movement beta rebound.

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Optically pumped magnetometers (OPMs) are an emerging lightweight and compact sensor that can measure magnetic fields generated by the human brain. OPMs enable construction of wearable magnetoencephalography (MEG) systems, which offer advantages over conventional instrumentation. However, when trying to measure signals at low frequency, higher levels of inherent sensor noise, magnetic interference and movement artefact introduce a significant challenge.

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Article Synopsis
  • Post-task responses (PTRs) are temporary brain activity changes that occur after completing a task, especially noted in beta band frequencies following movement.
  • This study investigated PTRs during a working-memory task using magnetoencephalography (MEG) in 20 healthy participants and found that PTRs were present across multiple brain regions, including those involved in higher cognition.
  • The results indicated that PTRs increase with cognitive load and are associated with reaction times, suggesting that they are a broader self-regulatory mechanism in the brain, not limited to motor activities.
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Ipsilateral sensorimotor (iSM1) cortex negative BOLD responses (NBR) are observed to unilateral tasks and are thought to reflect a functionally relevant component of sensorimotor inhibition. Evidence suggests that sensorimotor inhibitory mechanisms degrade with age, along with aspects of motor ability and dexterity. However, understanding of age-related changes to NBR is restricted by limited comparisons between young vs old adults groups with relatively small samples sizes.

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