Implicit and explicit emotional memory recall in anxiety and depression: Role of basolateral amygdala and cortisol-norepinephrine interaction.


Journal

Psychoneuroendocrinology
ISSN: 1873-3360
Titre abrégé: Psychoneuroendocrinology
Pays: England
ID NLM: 7612148

Informations de publication

Date de publication:
02 2022
Historique:
received: 23 08 2021
revised: 14 10 2021
accepted: 17 11 2021
pubmed: 12 12 2021
medline: 12 4 2022
entrez: 11 12 2021
Statut: ppublish

Résumé

Anxiety and depression are linked to both explicit and implicit memory biases, which are defined as the tendency to preferentially recall emotionally negative information at conscious and subconscious levels, respectively. Functional connectivity (FC) of the basolateral amygdala (BLA) and related stress hormones (i.e., cortisol and norepinephrine) are purportedly implicated in these biases. However, previous findings on memory biases in anxiety and depression have been inconsistent, likely due to their symptomatic complications. Therefore, the underlying neurobiological mechanism remains unclear. We thus investigated whether anxiety and depression as premorbid predispositions are related to the memory biases, and whether FC of BLA, cortisol, and 3-methoxy-4-hydroxyphenylglycol (MHPG: a major metabolite of norepinephrine) would affect the anxiety/depression-related biased memory recall in 100 participants without psychiatric symptomatology. Psycho-behavioral assessment, resting-state fMRI scans, and saliva collection at 10-points-in-time across two days were conducted. Correlations of memory biases with anxiety/depression and neurobiological markers were explored. As a result, neither anxiety nor depression were correlated with explicit memory bias to negative (vs. positive) information, although depression was associated with better recall of the negative stimuli only when they were perceived as self-relevant. In contrast, both anxiety and depression were correlated with implicit memory bias; however, the effects were solely explained by anxiety. Furthermore, FC of the BLA with subgenual anterior cingulate cortex (sgACC) and the synergetic effect of cortisol and MHPG uniquely affected the implicit memory bias. These findings suggest that anxiety facilitates an initial snapshot of negative information and can be accompanied by depression when the information creates negative semantic associations with the self. The BLA-sgACC neural connectivity and cortisol-norepinephrine interaction that are associated with the implicit memory bias might be one of the important neurobiological targets in the prevention and treatment for comorbid anxiety and depressive disorders.

Identifiants

pubmed: 34894424
pii: S0306-4530(21)00472-8
doi: 10.1016/j.psyneuen.2021.105598
pii:
doi:

Substances chimiques

Methoxyhydroxyphenylglycol 534-82-7
Hydrocortisone WI4X0X7BPJ
Norepinephrine X4W3ENH1CV

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105598

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Yuko Hakamata (Y)

Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry, Japan; Department of Health Science, Kitasato University School of Allied Health Sciences, Japan; Department of Clinical and Cognitive Neuroscience, Toyama University School of Medicine, Japan. Electronic address: hakamata@med.u-toyama.ac.jp.

Shinya Mizukami (S)

Department of Radiological Technology, Kitasato University School of Health Sciences, Japan.

Shuhei Izawa (S)

Occupational Stress Research Group, National Institute of Occupational Safety and Health, Japan.

Hisayoshi Okamura (H)

Cognitive and Molecular Research Institute of Brain Diseases, Kurume University School of Medicine, Japan.

Kengo Mihara (K)

Department of Human Community, Kyushu Ryukoku Junior College, Japan.

Hilary Marusak (H)

Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, United Staets of America.

Yoshiya Moriguchi (Y)

Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry, Japan.

Hiroaki Hori (H)

Department of Behavioral Medicine, National Institute of Mental Health, National Center of Neurology and Psychiatry, Japan.

Takashi Hanakawa (T)

Department of Integrated Neuroanatomy and Neuroimaging, Kyoto University, Japan.

Yusuke Inoue (Y)

Department of Diagnostic Radiology, Kitasato University School of Medicine, Japan.

Hirokuni Tagaya (H)

Department of Health Science, Kitasato University School of Allied Health Sciences, Japan.

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