Evidence map›Paper›PMID 30246167›Full record

ArticleChronic stress (Thousand Oaks, Calif.)

Maternal Cerebrospinal Fluid Glutamate in Response to Variable Foraging Demand: Relationship to Cerebrospinal Fluid Serotonin Metabolites in Grown Offspring.

Jeremy D Coplan, Nishant K Gupta, Sarah K Flynn, Wade J Reiner, David Gaita, Sasha L Fulton, Anna V Rozenboym, Jean E Tang, Thomas B Cooper, J John Mann

Open access · goldAbstract read
In one paragraph

Article in Chronic stress (Thousand Oaks, Calif.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Early life stress and glutamate neurotransmission in major depressive disorder.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2020
    Article
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

10 authors at 5 institutions in 1 country.

Jeremy D CoplanDepartment of Psychiatry and Behavioral Sciences, State University of New York Downstate Medical Center, Brooklyn, NY, USA.
Nishant K GuptaCollege of Medicine, State University of New York Downstate Medical Center, Brooklyn, NY, USA.ORCID 0000-0002-8006-3786
Sarah K FlynnCollege of Medicine, State University of New York Downstate Medical Center, Brooklyn, NY, USA.
Wade J ReinerCollege of Medicine, State University of New York Downstate Medical Center, Brooklyn, NY, USA.
David GaitaCollege of Medicine, State University of New York Downstate Medical Center, Brooklyn, NY, USA.
Sasha L FultonDepartment of Psychiatry, College of Physicians and Surgeons, Columbia University Medical Center, New York State Psychiatric Institute, New York, NY, USA.ORCID 0000-0003-3626-7412
Anna V RozenboymDepartment of Biological Sciences, Kingsborough Community College, City University of New York, Brooklyn, NY, USA.
Jean E TangDepartment of Psychiatry, College of Physicians and Surgeons, Columbia University Medical Center, New York State Psychiatric Institute, New York, NY, USA.
Thomas B CooperDepartment of Psychopharmacology, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
J John MannDepartment of Psychiatry, Columbia University, New York, NY, USA.ORCID 0000-0002-0265-6586
State University of New York · USColumbia University Irving Medical Center · USCity University of New York · USNathan Kline Institute for Psychiatric Research · USNew York Psychoanalytic Society and Institute · US

Funding

Neurobiology of Depression and AntidepressantsR01MH040695 · NIMH · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI MANN, JOSEPH JOHN · 1986 to 2014
$7.1M
ADVERSE EARLY REARING &GLUTAMATERGIC FUNCTIONR01MH059990 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI COPLAN, JEREMY D · 2000 to 2003
$1.1M
NIMH NIH HHS R01 MH040695NIMH NIH HHS R01 MH059990
6 · The paper itself

Abstract

backgroundMaternal response to allostatic overload during infant rearing may alter neurobiological measures in grown offspring, potentially increasing susceptibility to mood and anxiety disorders. We examined maternal cerebrospinal fluid (CSF) glutamate response during exposure to variable foraging demand (VFD), a bonnet macaque model of allostatic overload, testing whether activation relative to baseline predicted concomitant CSF elevations of the stress neuropeptide, corticotropin-releasing factor. We investigated whether VFD-induced activation of maternal CSF glutamate affects maternal-infant attachment patterns and offspring CSF 5-hydroxyindoleacetic acid concentrations.

methodsMother-infant dyads were exposed to the "VFD stressor," a paradigm in which mothers experience 16 weeks of foraging uncertainty while rearing their infant offspring. Through staggering the infant age of VFD onset, both a cross-sectional design and a longitudinal design were used. Maternal CSF glutamate and glutamine concentrations post-VFD exposure were cross-sectionally compared to maternal VFD naive controls. Proportional change in concentrations of maternal glutamate (and glutamine), a longitudinal measure, was evaluated in relation to VFD-induced elevations of CSF corticotropin-releasing factor. The former measure was related to maternal-infant proximity scores obtained during the final phases of VFD exposure. Maternal glutamatergic response to VFD exposure was used as a predictor variable for young adolescent offspring CSF metabolites of serotonin, dopamine, and norepinephrine.

resultsFollowing VFD exposure, maternal CSF glutamate concentrations correlated positively with maternal CSF CRF concentrations. Activation relative to baseline of maternal CSF glutamate concentrations following VFD exposure correlated directly with a) increased maternal-infant proximity during the final phases of VFD and b) offspring CSF concentrations of monoamine metabolites including 5-hydroxyindoleacetic acid, which was elevated relative to controls.

conclusionsActivation of maternal CSF glutamate in response to VFD-induced allostasis is directly associated with elevations of maternal CSF corticotropin-releasing factor. Maternal CSF glutamate alterations induced by VFD potentially compromise serotonin neurotransmission in grown offspring, conceivably modeling human vulnerability to treatment-resistant mood and anxiety disorders.

Indexed as

corticotropin-releasing factorearly life stressglutamatenonhuman primatesserotoninvariable foraging demand

Identifiers

PMID30246167
PMCPMC6145812
OpenAlexW2833557252

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.