Molecular neurobiology of loss: a role for basolateral amygdala extracellular matrix

被引:0
作者
Marissa A. Smail
Brittany L. Smith
Rammohan Shukla
Khaled Alganem
Hunter M. Eby
Justin L. Bollinger
Ria K. Parikh
James B. Chambers
James K. Reigle
Rachel D. Moloney
Nawshaba Nawreen
Eric S. Wohleb
Harry Pantazopoulos
Robert E. McCullumsmith
James P. Herman
机构
[1] University of Cincinnati,Department of Pharmacology and Systems Physiology
[2] University of Cincinnati,Neuroscience Graduate Program
[3] University of Toledo,Department of Neurosciences
[4] Cincinnati Children’s Hospital Medical Center,Department of Biomedical Informatics
[5] University College Cork,School of Pharmacy
[6] University College Cork,Department of Pharmacology and Therapeutics
[7] University College Cork,APC Microbiome Ireland
[8] University of Mississippi Medical Center,Department of Neurobiology and Anatomical Sciences
[9] Neurosciences Institute,Department of Neurology
[10] ProMedica,undefined
[11] Veterans Affairs Medical Center,undefined
[12] University of Cincinnati,undefined
来源
Molecular Psychiatry | 2023年 / 28卷
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摘要
Psychological loss is a common experience that erodes well-being and negatively impacts quality of life. The molecular underpinnings of loss are poorly understood. Here, we investigate the mechanisms of loss using an environmental enrichment removal (ER) paradigm in male rats. The basolateral amygdala (BLA) was identified as a region of interest, demonstrating differential Fos responsivity to ER and having an established role in stress processing and adaptation. A comprehensive multi-omics investigation of the BLA, spanning multiple cohorts, platforms, and analyses, revealed alterations in microglia and the extracellular matrix (ECM). Follow-up studies indicated that ER decreased microglia size, complexity, and phagocytosis, suggesting reduced immune surveillance. Loss also substantially increased ECM coverage, specifically targeting perineuronal nets surrounding parvalbumin interneurons, suggesting decreased plasticity and increased inhibition within the BLA following loss. Behavioral analyses suggest that these molecular effects are linked to impaired BLA salience evaluation, leading to a mismatch between stimulus and reaction intensity. These loss-like behaviors could be rescued by depleting BLA ECM during the removal period, helping us understand the mechanisms underlying loss and revealing novel molecular targets to ameliorate its impact.
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页码:4729 / 4741
页数:12
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