Evidence map›Paper›PMID 37644175›Full record

ArticleMolecular psychiatry2023

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

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 and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Molecular Characterization of the Progressive Landscape of Depression.bioRxiv : the preprint server for biology · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 2 countries.

Marissa A SmailDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA. smailma@mail.uc.edu.ORCID 0000-0002-9743-3771
Brittany L SmithDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
Rammohan ShuklaDepartment of Neurosciences, University of Toledo, Toledo, OH, USA.ORCID 0000-0001-5776-2506
Khaled AlganemDepartment of Neurosciences, University of Toledo, Toledo, OH, USA.
Hunter M EbyDepartment of Neurosciences, University of Toledo, Toledo, OH, USA.
Justin L BollingerDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
Ria K ParikhDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
James B ChambersDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
James K ReigleDepartment of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Rachel D MoloneySchool of Pharmacy, University College Cork, Cork, Ireland, UK.
Nawshaba NawreenDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
Eric S WohlebDepartment of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.
Harry PantazopoulosDepartment of Neurobiology and Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS, USA.ORCID 0000-0002-8905-8377
Robert E McCullumsmith *Department of Neurosciences, University of Toledo, Toledo, OH, USA.ORCID 0000-0001-6921-7150
James P Herman *Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, OH, USA.ORCID 0000-0003-3571-2406
University of Cincinnati · USUniversity of Toledo · USCincinnati Children's Hospital Medical Center · USNeurosciences Institute · USUniversity College Cork · IEUniversity of Mississippi Medical Center · USVeterans Health Administration · US

Funding

FUNCTIONAL ANATOMY OF LIMBIC NEUROENDOCRINE CIRCUITSR01MH049698 · NIMH · UNIVERSITY OF KENTUCKY · PI HERMAN, JAMES P · 1998 to 2018
$6.2M
Translational assessment of brain bioenergetic function in schizophreniaR01MH121102 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI MARANO, CHRISTOPHER, MCCULLUMSMITH, ROBERT E · 2020 to 2024
$3.7M
Cortical Mechanisms of Traumatic StressR01MH127835 · NIMH · UNIVERSITY OF CINCINNATI · PI James P Herman · 2022 to 2026
$2.9M
Stress resilience by natural rewards: neurocircuit mechanismsR01MH119814 · NIMH · UNIVERSITY OF CINCINNATI · PI HERMAN, JAMES P, ULRICH-LAI, YVONNE MICHELLE · 2019 to 2023
$2.9M
Cell-specific analysis of sub-kinomes in schizophreniaR01MH107487 · NIMH · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI MCCULLUMSMITH, ROBERT E, MELLER, JAREK · 2016 to 2020
$1.9M
Neurobiology of loss: role of microgliaF31MH125541 · NIMH · UNIVERSITY OF CINCINNATI · PI SMAIL, MARISSA ANN · 2021 to 2023
$102k
FUNCTIONAL ANATOMY OF LIMBIC/NEUROENDOCRINE CIRCUITSR29MH049698 · NIMH · UNIVERSITY OF KENTUCKY · PI HERMAN, JAMES P · 1992 to 1996
–
NIMH NIH HHS F31 MH125541NIMH NIH HHS R01 MH049698NIMH NIH HHS R01 MH107487NIMH NIH HHS R01 MH119814NIMH NIH HHS R01 MH121102NIMH NIH HHS R01 MH127835
6 · The paper itself

Abstract

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.

Indexed as

Basolateral Nuclear ComplexAnimalsExtracellular MatrixInterneuronsMaleNeurobiologyQuality of LifeRats

Identifiers

PMID37644175
PMCPMC10914625
OpenAlexW4386254827

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.