Inhibitory temporo-parietal effective connectivity is associated with explicit memory performance in older adults.

Behavioral neuroscience Cognitive neuroscience Neuroscience Techniques in neuroscience

Journal

iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038

Informations de publication

Date de publication:
20 Oct 2023
Historique:
received: 05 01 2023
revised: 30 06 2023
accepted: 25 08 2023
medline: 25 9 2023
pubmed: 25 9 2023
entrez: 25 9 2023
Statut: epublish

Résumé

Successful explicit memory encoding is associated with inferior temporal activations and medial parietal deactivations, which are attenuated in aging. Here we used dynamic causal modeling (DCM) of functional magnetic resonance imaging data to elucidate effective connectivity patterns between hippocampus, parahippocampal place area (PPA), and precuneus during encoding of novel visual scenes. In 117 young adults, DCM revealed pronounced activating input from the PPA to the hippocampus and inhibitory connectivity from the PPA to the precuneus during novelty processing, with both being enhanced during successful encoding. This pattern could be replicated in two cohorts (N = 141 and 148) of young and older adults. In both cohorts, older adults selectively exhibited attenuated inhibitory PPA-precuneus connectivity, which correlated negatively with memory performance. Our results provide insight into the network dynamics underlying explicit memory encoding and suggest that age-related differences in memory-related network activity are, at least partly, attributable to altered temporo-parietal neocortical connectivity.

Identifiants

pubmed: 37744028
doi: 10.1016/j.isci.2023.107765
pii: S2589-0042(23)01842-4
pmc: PMC10514462
doi:

Types de publication

Journal Article

Langues

eng

Pagination

107765

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors declare no competing interests.

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Auteurs

Björn H Schott (BH)

German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Leibniz Institute for Neurobiology (LIN), Magdeburg, Germany.
Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany.
Department of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany.

Joram Soch (J)

German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Bernstein Center for Computational Neuroscience (BCCN), Berlin, Germany.

Jasmin M Kizilirmak (JM)

German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Neurodidactics and NeuroLab, Institute for Psychology, University of Hildesheim, Hildesheim, Germany.

Hartmut Schütze (H)

German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Otto von Guericke University, Medical Faculty, Magdeburg, Germany.

Anne Assmann (A)

German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Otto von Guericke University, Medical Faculty, Magdeburg, Germany.

Anne Maass (A)

German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.

Gabriel Ziegler (G)

German Center for Neurodegenerative Diseases (DZNE), Magdeburg, Germany.
Otto von Guericke University, Medical Faculty, Magdeburg, Germany.

Magdalena Sauvage (M)

Leibniz Institute for Neurobiology (LIN), Magdeburg, Germany.

Anni Richter (A)

Leibniz Institute for Neurobiology (LIN), Magdeburg, Germany.
German Center for Mental Health (DZPG), Magdeburg, Germany.
Center for Intervention and Research on adaptive and Maladaptive Brain Circuits Underlying Mental Health (C-I-R-C) Jena-Magdeburg-Halle, Magdeburg, Germany.

Classifications MeSH