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Steven L. Bressler
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Journal Articles
Publisher: Journals Gateway
Journal of Cognitive Neuroscience (2015) 27 (4): 639–654.
Published: 01 April 2015
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The pFC enables the essential human capacities for predicting future events and preadapting to them. These capacities rest on both the structure and dynamics of the human pFC. Structurally, pFC, together with posterior association cortex, is at the highest hierarchical level of cortical organization, harboring neural networks that represent complex goal-directed actions. Dynamically, pFC is at the highest level of the perception–action cycle, the circular processing loop through the cortex that interfaces the organism with the environment in the pursuit of goals. In its predictive and preadaptive roles, pFC supports cognitive functions that are critical for the temporal organization of future behavior, including planning, attentional set, working memory, decision-making, and error monitoring. These functions have a common future perspective and are dynamically intertwined in goal-directed action. They all utilize the same neural infrastructure: a vast array of widely distributed, overlapping, and interactive cortical networks of personal memory and semantic knowledge, named cognits, which are formed by synaptic reinforcement in learning and memory acquisition. From this cortex-wide reservoir of memory and knowledge, pFC generates purposeful, goal-directed actions that are preadapted to predicted future events.
Journal Articles
Publisher: Journals Gateway
Journal of Cognitive Neuroscience (2008) 20 (10): 1915–1925.
Published: 01 October 2008
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Response time (RT) is an important behavioral measure of the overall efficacy of sensorimotor processing and is known to vary significantly from trial to trial. Past work on how stimulus evoked cortical responses contribute to RT variability has helped delineate the stages of neuronal information processing. Much less is known about how the state of the brain immediately preceding the stimulus onset (prestimulus) affects RT. We addressed this problem by analyzing data from three macaque monkeys trained to perform a visuomotor pattern discrimination task. Local field potentials were recorded from up to 16 bipolar surface-to-depth electrodes widely distributed over one cerebral hemisphere in each monkey. The degree of linear correlation between RT and prestimulus spectral power was determined over a wide range of frequencies. In the prefrontal cortex, prestimulus power in the beta range (14–30 Hz) was negatively correlated with RT in two monkeys, suggesting a possible role of activity in this frequency range in the mediation of top-down control of visuomotor processing. In the sensorimotor cortex, prestimulus power in the beta range was positively correlated with RT in two monkeys, consistent with the hypothesis that oscillations in this range support the maintenance of steady-state motor output. In visual occipital and temporal lobe areas, prestimulus power in the alpha/low beta range (8–20 Hz) showed positive correlations with RT in three monkeys, possibly reflecting a spatially specific disengagement of visual anticipatory attention. Through measurement of prestimulus spectral coherence, it was further determined that sites showing similar patterns of correlation between spectral power and RT were also linked together in synchronized networks.