Stimulus-driven actions are preceded by preparatory brain activity that can be expressed by event-related potentials (ERP). Literature on this topic has focused on simple actions, such as the finger keypress, finding activity in frontal, parietal, and occipital areas detectable up to two seconds before the stimulus onset. Little is known about the preparatory brain activity when the action complexity increases, and specific brain areas designated to achieve movement integration intervene. This paper aims to identify the time course of preparatory brain activity associated with actions of increasing complexity using ERP analysis and a visuomotor discrimination task. Motor complexity was manipulated by asking nineteen volunteers to provide their response by simply pressing a key or by adding to the keypress arm extensions alone, or in combination with a standing step (involving the whole body). Results showed that these actions of increasing levels of complexity appear to be associated with different patterns of preparatory brain activity in which the found components were differently modulated. The simple keypress was characterized by the prominent motor excitatory preparation in premotor areas paralleled by the largest prefrontal inhibitory/attentional control. Reaching presented a dominant parietal preparation confirming the role of these integration areas in reaching actions toward a goal. Stepping was characterized by localized activity in the bilateral dorsomedial parieto-occipital areas attributable to sensory readiness, for the approaching stimulus. In conclusion, the brain can optimally anticipate any stimulus-driven action modulating the activity in the brain areas specialized in the preparation of that action type.
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http://dx.doi.org/10.1016/j.biopsycho.2024.108959 | DOI Listing |
Front Psychol
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Department of Neurobiology and Biophysics, University of Washington, Seattle, WA, United States.
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State Key Laboratory of Ophthalmology, Optometry and Vision Science, Wenzhou Medical University, Wenzhou, Zhejiang 325027, China.
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January 2025
Department of Radiology, Molecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, Stanford, CA, 94305, USA.
Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumor in adults, characterized by resistance to conventional therapies and poor survival. Ferroptosis, a form of regulated cell death driven by lipid peroxidation, has recently emerged as a promising therapeutic target for GBM treatment. However, there are currently no non-invasive imaging techniques to monitor the engagement of pro-ferroptotic compounds with their respective targets, or to monitor the efficacy of ferroptosis-based therapies.
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