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J Neurosci. 2010 Aug 18;30(33):10967-76. doi: 10.1523/JNEUROSCI.2611-10.2010.

Separable prefrontal cortex contributions to free recall.

Author information

1
Department of Cognitive, Linguistic, and Psychological Sciences, Brown University, Providence, Rhode Island 02912, USA. niclong@sas.upenn.edu

Abstract

In everyday life, we often must remember the past in the absence of helpful cues in the environment. In these cases, the brain directs retrieval by relying on internally maintained cues and strategies. Free recall is a widely used behavioral paradigm for studying retrieval with minimal cue support. During free recall, individuals often recall semantically related items consecutively--an effect termed semantic clustering--and previous studies have sought to understand clustering to gain leverage on the basic mechanisms supporting strategic recall. Successful recall and semantic clustering depend on the prefrontal cortex (PFC). However, as a result of methodological limitations, few functional magnetic resonance imaging (fMRI) studies have assessed the neural mechanisms at encoding that support subsequent recall, and none have tested the event-related correlates of recall itself. Thus, it remains open whether one or several frontal control mechanisms operate during encoding and recall. Here, we applied a recently developed method (Oztekin et al., 2010) to assess event-related fMRI signal changes during free recall. During encoding, dorsolateral prefrontal cortex (DLPFC) activation was predictive of subsequent semantic clustering. In contrast, subregions of ventrolateral prefrontal cortex (VLPFC) were predictive of subsequent recall, whether clustered or nonclustered, and were inversely associated with clustering during recall. These results suggest that DLPFC supports relational processes at encoding that are sufficient to produce category clustering effects during recall. Conversely, controlled retrieval mechanisms supported by VLPFC support item-specific search during recall.

PMID:
20720103
PMCID:
PMC3265965
DOI:
10.1523/JNEUROSCI.2611-10.2010
[Indexed for MEDLINE]
Free PMC Article

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