Normal human behavior and cognition are reliant on a person's ability to inhibit inappropriate thoughts, impulses, and actions. The temporal and spatial advantages of event-related functional MRI (fMRI) were exploited to identify cortical regions that showed a transient change in fMRI signal after the withholding of a prepotent motor response. The temporal specificity of the event-related fMRI design also minimized possible contamination from response inhibition errors (i. e., commission errors) and other extraneous processes. Regions identified were strongly lateralized to the right hemisphere and included the middle and inferior frontal gyri, frontal limbic area, anterior insula, and inferior parietal lobe. Contrary to the prominence traditionally given to ventral frontal regions for response inhibition, the results suggest that response inhibition is accomplished by a distributed cortical network.

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Objective: Cocaine-related cues have been hypothesized to perpetuate drug abuse by inducing a craving response that prompts drug-seeking behavior. However, the mechanisms, underlying neuroanatomy, and specificity of this neuroanatomy are not yet fully understood.Method: To address these issues, experienced cocaine users (N=17) and comparison subjects (N=14) underwent functional magnetic resonance imaging while viewing three separate films that portrayed 1 ) individuals smoking crack cocaine, 2) outdoor nature scenes, and 3) explicit sexual content. Candidate craving sites were identified as those that showed significant activation in the cocaine users when viewing the cocaine film. These sites were then required to show significantly greater activation when contrasted with comparison subjects viewing the cocaine film (population specificity) and cocaine users viewing the nature film (content specificity).Results: Brain regions that satisfied these criteria were largely left lateralized and included the frontal lobe (medial and middle frontal gyri, bilateral inferior frontal gyrus), parietal lobe (bilateral inferior parietal lobule), insula, and limbic lobe (anterior and posterior cingulate gyrus). Of the 13 regions identified as putative craving sites, just three (anterior cingulate, right inferior parietal lobule, and the caudate/ lateral dorsal nucleus) showed significantly greater activation during the cocaine film than during the sex film in the cocaine users, which suggests that cocaine cues activated similar neuroanatomical substrates as naturally evocative stimuli in the cocaine users. Finally, contrary to the effects of the cocaine film, cocaine users showed a smaller response than the comparison subjects to the sex film.Conclusions: These data suggest that cocaine craving is not associated with a dedicated and unique neuroanatomical circuitry; instead, unique to the cocaine user is the ability of learned, drug-related cues to produce brain activation comparable to that seen with nondrug evocative stimuli in healthy comparison subjects.

The default mode network (DMN) in humans has been suggested to support a variety of cognitive functions and has been implicated in an array of neuropsychological disorders. However, its function (s) remains poorly understood. We show that rats possess a DMN that is broadly similar to the DMNs of nonhuman primates and humans. Our data suggest that, despite the distinct evolutionary paths between rodent and primate brain, a well-organized, intrinsically coherent DMN appears to be a fundamental feature in the mammalian brain whose primary functions might be to integrate multimodal sensory and affective information to guide behavior in anticipation of changing environmental contingencies.functional MRI | resting state | intrinsic activity | connectivity | spontaneous fluctuation I n the absence of an immediate need for goal-directed attention to the surrounding environment, our minds wander from recollection of past happenings to imagination of future events. Neuroimaging studies have consistently identified a set of interconnected brain areas that becomes less active during attentiondemanding cognitive tasks (1). This so-called default mode network (DMN) is posited to play a fundamental role in brain organization and supports a variety of self-referential functions such as understanding others' mental state, recollection and imagination (2), conceptual processing (3), and even in the sustenance of conscious awareness (4). Many of these functions have been considered to be unique to humans. Intriguingly, similar coherent structures have been shown to exist in anesthetized macaque monkeys and chimpanzees (5, 6). Furthermore, the functions of the default network are disrupted in such neuropsychological disorders as schizophrenia, Alzheimer's disease, and autism (7-9), underscoring the clear and critical need for further investigating the neurobiological basis of DMN using animal models.The evolutionary clade of rodents is about 35 million years earlier than that of old world monkeys and about 60 million years earlier than humans (10). Although many of the structures and functions of subcortical nuclei are conserved across these three species, the neocortex, in particular the "association" cortex, has extensively expanded in the primate as a result of evolutionary pressure, which is considered to be crucial in the development of higher cognitive and behavioral functions (10, 11). On the other hand, such structures as cingulate cortex, prefrontal cortex, and hippocampal formation, all of which are critical elements of the DMN, are also present in rodents (11). Given the distant evolutionary paths between rodent and primate brain, an intriguing question arises: Does the rat possess a similar DMN? Such a network, once demonstrated, would not only suggest that an operational DMN is a common feature in the mammalian brain, perhaps induced via parallel evolution as a result of natural selection, it would also offer a novel platform to explore the physiological basis and behavioral significance of the DMN. Such a demonstratio...