2006
DOI: 10.1111/j.1460-9568.2006.04824.x
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Time is a rubberband: neuronal activity in monkey motor cortex in relation to time estimation

Abstract: Anticipation of predictable events is crucial for organizing motor performance. Using instructed delay tasks, it has been shown that even when delay duration is kept constant, reaction time fluctuates from trial to trial. As time estimation is at the core of anticipatory behavior, it is reasonable to speculate whether neuronal delay activity correlates with the subjective estimate of time. As a consequence of the scalar property of time estimation processes, the variability in time estimation increases continu… Show more

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Cited by 61 publications
(65 citation statements)
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“…This widespread phenomenon of preactivation was only observed with predictable cue timing. However, its function is still unclear: it could participate in a general timing process of the cue (Durstewitz, 2004;Nobre, 2008, Fujioka et al, 2012), or be part of a preparatory process in anticipation of a future motor event, similar to what was found before movement onset (Lucchetti and Bon, 2001;Renoult et al, 2006;Lebedev et al, 2008).…”
Section: Introductionmentioning
confidence: 52%
“…This widespread phenomenon of preactivation was only observed with predictable cue timing. However, its function is still unclear: it could participate in a general timing process of the cue (Durstewitz, 2004;Nobre, 2008, Fujioka et al, 2012), or be part of a preparatory process in anticipation of a future motor event, similar to what was found before movement onset (Lucchetti and Bon, 2001;Renoult et al, 2006;Lebedev et al, 2008).…”
Section: Introductionmentioning
confidence: 52%
“…For example, neural activity related to elapsed time has been reported in prefrontal cortex during duration reproduction (Jech et al, 2005), and in LIP during time interval (Leon and Shadlen, 2003) and motion discrimination (Churchland et al, 2008). During instructed delays with different possible durations, as each of the likely GO signal times approaches there is a buildup of neural activity in LIP during saccade tasks (Janssen and Shadlen, 2005), and in motor cortex during reaching tasks (Renoult et al, 2006), with corresponding changes of corticospinal excitability (van Elswijk et al, 2007). More generally, buildup activity has been reported in a variety of brain regions even during motor tasks that do not involve any decisions (Hanes and Schall, 1996;Munoz et al, 2000;Ivry and Spencer, 2004;Roesch and Olson, 2005;Tanaka, 2007;Thomas and Paré, 2007;Lebedev et al, 2008).…”
Section: Discussionmentioning
confidence: 99%
“…Studies report that temporal estimates of planned movements are encoded by populations of single neurons that monotonically modulate firing rate in proportion to the estimate, referred to as temporal scaling (Merchant et al, 2013a;Wittmann, 2013). Such neuronal behavior has been identified throughout the cortex (Goldman-Rakic, 1995;Crammond and Kalaska, 2000;Matell et al, 2003Matell et al, , 2011Roux et al, 2003;Lebedev et al, , 2008Reutimann et al, 2004;Merchant et al, 2004a, b;Janssen and Shadlen, 2005;Merchant and Georgopoulos, 2006;Maimon and Assad, 2006;Renoult et al, 2006;Genovesio et al, 2009;Mita et al, 2009;Knudsen et al, 2012;Kim et al, 2013) and across different behavioral tasks. We recently extended this phenomena to subpopulations of neurons within the hindlimb sensorimotor cortex (HLSMC) of rats producing timed hindlimb movements (Knudsen et al, 2012).…”
Section: Introductionmentioning
confidence: 99%