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Object unitization and associative memory formation are supported by distinct brain regions.

ABSTRACT: While it has been established that the medial temporal lobe (MTL) is critical for successful memory formation, the precise contribution of one of the key MTL subregions, the perirhinal cortex (PrC), has been the subject of intense focus and debate. Although this region has been implicated in nonassociative item encoding, recent neuroimaging data have revealed that it also contributes to the binding of specific item-related associations (e.g., an object-color association). Based on neuropsychological evidence that associative memory for unitized word pairs does not require the hippocampus, it has been proposed that PrC contributes to associative memory formation by means of unitization. However, the role of PrC in unitization processes remains unclear. Here, we used fMRI to assess the involvement of PrC in object unitization as well as in successful episodic encoding of item-related details. Our results show that while PrC activation linearly tracks the amount of item-related information successfully encoded, it is not modulated by object unitization demands. Instead, the present data reveal that unitization of object fragments may be accomplished in visual/ventral temporal processing stages before PrC. Indeed, we observed a gradual transition from unitization to successful memory formation across the ventral visual pathway. This suggests that PrC may specifically serve to encode item-related event details, whereas their perceptual integration is established along preceding processing stages.

SUBMITTER: Staresina BP

PROVIDER: S-EPMC2927970 | biostudies-literature | 2010 Jul

REPOSITORIES: biostudies-literature

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Object unitization and associative memory formation are supported by distinct brain regions.

Staresina Bernhard P BP Davachi Lila L

The Journal of neuroscience : the official journal of the Society for Neuroscience 20100701 29

While it has been established that the medial temporal lobe (MTL) is critical for successful memory formation, the precise contribution of one of the key MTL subregions, the perirhinal cortex (PrC), has been the subject of intense focus and debate. Although this region has been implicated in nonassociative item encoding, recent neuroimaging data have revealed that it also contributes to the binding of specific item-related associations (e.g., an object-color association). Based on neuropsycholog ...[more]

PMID: 20660271

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Project description:BackgroundStudying structural brain aging is important to understand age-related pathologies, as well as to identify the early manifestations of the Alzheimer's disease (AD) continuum. In this study, we investigated the long-term trajectory of physiological and pathological brain aging in a large number of participants ranging from the 50s to over 80 years of age.ObjectiveTo explore the distinct brain regions that distinguish pathological brain aging from physiological brain aging using sophisticated measurements of cortical thickness.MethodsA total of 2,823 cognitively normal (CN) individuals and 2,675 patients with AD continuum [874 with subjective memory impairment (SMI), 954 with amnestic mild cognitive impairment (aMCI), and 847 with AD dementia] who underwent a high-resolution 3.0-tesla MRI were included in this study. To investigate pathological brain aging, we further classified patients with aMCI and AD according to the severity of cognitive impairment. Cortical thickness was measured using a surface-based method. Multiple linear regression analyses were performed to evaluate age, diagnostic groups, and cortical thickness.ResultsAging extensively affected cortical thickness not only in CN individuals but also in AD continuum patients; however, the precuneus and inferior temporal regions were relatively preserved against age-related cortical thinning. Compared to CN individuals, AD continuum patients including those with SMI showed a decreased cortical thickness in the perisylvian region. However, widespread cortical thinning including the precuneus and inferior temporal regions were found from the late-stage aMCI to the moderate to severe AD. Unlike the other age groups, AD continuum patients aged over 80 years showed prominent cortical thinning in the medial temporal region with relative sparing of the precuneus.ConclusionOur findings suggested that the precuneus and inferior temporal regions are the key regions in distinguishing between physiological and pathological brain aging. Attempts to differentiate age-related pathology from physiological brain aging at a very early stage would be important in terms of establishing new strategies for preventing accelerated pathological brain aging.

Dataset Information

Object unitization and associative memory formation are supported by distinct brain regions.

Publications

Object unitization and associative memory formation are supported by distinct brain regions.

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