We combined the data of five event-related fMRI studies of response inhibition. The reanalysis (n = 71) revealed response inhibition to be accomplished by a largely right hemisphere network of prefrontal, parietal, subcortical and midline regions, with converging evidence pointing to the particular importance of the right frontal operculum.Functional differences were observed between the sexes with greater activity in females in many of these cortical regions. Despite the relatively narrow age range (18-46), cortical activity, on the whole, tended to increase with age, echoing a pattern of functional recruitment often observed in the elderly. More absentminded subjects showed greater activity in fronto-parietal areas, while speed of Go trial responses produced a varied pattern of activation differences in more posterior and subcortical areas. Although response inhibition produces robust activation in a discrete network of brain regions, these results reveal that individual differences impact on the relative contribution made by the nodes of this network.
IntroductionDifficulty inhibiting inappropriate behaviours is characteristic of many psychological and psychiatric disorders ranging from the impulsivity of children with ADHD (Barkley, 1997), the loss of control exhibited by drug abusers (Fillmore and Rush, 2002;Kaufman et al., 2003), to the inappropriate stimulus-driven behaviour of brain-damaged individuals (Luria, 1966). Normal cognition is also subject to occasional inhibitory disruption as suggested by lapses in speech, action, thought and intention, wherein behaviour appears to be dictated by cue or by habit (Dempster and Brainerd, 1995). As a result of the apparent importance of this aspect of cognitive control, much effort has been expended in attempting to identify its neuroanatomical substrates. However, inhibitory control is a broad term incorporating cognitive (e.g., suppressing interference), perceptual/attention (e.g., ignoring distracters) and motor (e.g., response countermanding) domains. While the similarities and dissimilarities between these aspects of inhibition remain unclear (Bunge et al., 2002;Friedman and Miyake, 2004), it is the latter operationalisation that will be the focus here. A substantial body of evidence on motor inhibition now exists due, in part, to the relative ease of implementing experimental tests of this function. Previous neuroimaging research has converged on a discrete number of regions thought to be implicated in motor response inhibition including dorsolateral and ventrolateral prefrontal cortex, parietal cortex, midline regions including the anterior cingulate and pre-SMA, and there is also evidence for thalamic and subcortical involvement (Aron and Poldrack, 2006;Brass et al., 2001;Braver et al., 2001;Garavan et al., 1999;Menon et al., 2001;Rubia et al., 2001;Watanabe et al., 2002). More specifically, ventral regions of the right hemisphere appear to be particularly important; the frontal operculum has been implicated