Literature DB >> 35597233

Loss of functional heterogeneity along the CA3 transverse axis in aging.

Heekyung Lee1, Zitong Wang2, Arjuna Tillekeratne3, Nick Lukish3, Vyash Puliyadi4, Scott Zeger2, Michela Gallagher5, James J Knierim6.   

Abstract

Age-related deficits in pattern separation have been postulated to bias the output of hippocampal memory processing toward pattern completion, which can cause deficits in accurate memory retrieval. Although the CA3 region of the hippocampus is often conceptualized as a homogeneous network involved in pattern completion, growing evidence demonstrates a functional gradient in CA3 along the transverse axis, as pattern-separated outputs (dominant in the more proximal CA3) transition to pattern-completed outputs (dominant in the more distal CA3). We examined the neural representations along the CA3 transverse axis in young (Y), aged memory-unimpaired (AU), and aged memory-impaired (AI) rats when different changes were made to the environment. Functional heterogeneity in CA3 was observed in Y and AU rats when the environmental similarity was high (altered cues or altered environment shapes in the same room), with more orthogonalized representations in proximal CA3 than in distal CA3. In contrast, AI rats showed reduced orthogonalization in proximal CA3 but showed normal (i.e., generalized) representations in distal CA3, with little evidence of a functional gradient. Under experimental conditions when the environmental similarity was low (different rooms), representations in proximal and distal CA3 remapped in all rats, showing that CA3 of AI rats is able to encode distinctive representations for inputs with greater dissimilarity. These experiments support the hypotheses that the age-related bias toward hippocampal pattern completion is due to the loss in AI rats of the normal transition from pattern separation to pattern completion along the CA3 transverse axis.
Copyright © 2022 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CA3; aging; hippocampus; hyperactivity; memory impairment; pattern completion; pattern separation; place cells; remapping

Mesh:

Year:  2022        PMID: 35597233      PMCID: PMC9233142          DOI: 10.1016/j.cub.2022.04.077

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.900


  81 in total

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Journal:  Science       Date:  2005-07-22       Impact factor: 47.728

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Review 3.  Framing spatial cognition: neural representations of proximal and distal frames of reference and their roles in navigation.

Authors:  James J Knierim; Derek A Hamilton
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Authors:  Lisa Emery; Sandra Hale; Joel Myerson
Journal:  Psychol Aging       Date:  2008-09

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Journal:  Hippocampus       Date:  1998       Impact factor: 3.899

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Journal:  Hippocampus       Date:  1996       Impact factor: 3.899

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Journal:  J Comp Neurol       Date:  1997-09-01       Impact factor: 3.215

8.  Reelin in the Years: decline in the number of reelin immunoreactive neurons in layer II of the entorhinal cortex in aged monkeys with memory impairment.

Authors:  Jeffrey M Long; Evelyn J Perez; Jeffrey A Roberts; Mary T Roberts; Peter R Rapp
Journal:  Neurobiol Aging       Date:  2019-12-19       Impact factor: 4.673

9.  Reduced cognitive performance in aged rats correlates with increased excitation/inhibition ratio in the dentate gyrus in response to lateral entorhinal input.

Authors:  Trinh Tran; Michelle Bridi; Ming Teng Koh; Michela Gallagher; Alfredo Kirkwood
Journal:  Neurobiol Aging       Date:  2019-07-23       Impact factor: 5.133

10.  Response of the medial temporal lobe network in amnestic mild cognitive impairment to therapeutic intervention assessed by fMRI and memory task performance.

Authors:  Arnold Bakker; Marilyn S Albert; Gregory Krauss; Caroline L Speck; Michela Gallagher
Journal:  Neuroimage Clin       Date:  2015-02-21       Impact factor: 4.881

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