Evidence map›Paper›PMID 26699926›Full record

ArticleJournal of neurotrauma2016

Primary Blast Exposure Increases Hippocampal Vulnerability to Subsequent Exposure: Reducing Long-Term Potentiation.

Gwen B Effgen, Tiffany Ong, Shruthi Nammalwar, Andrea I Ortuño, David F Meaney, Cameron R 'Dale' Bass, Barclay Morrison

Abstract read
In one paragraph

Article in Journal of neurotrauma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Preclinical Models of Traumatic Brain Injury: Advances in In Vitro Models.Current neurology and neuroscience reports · 2026
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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

7 authors at 3 institutions in 1 country.

Gwen B Effgen1 Department of Biomedical Engineering, Columbia University , New York, New York.
Tiffany Ong1 Department of Biomedical Engineering, Columbia University , New York, New York.
Shruthi Nammalwar1 Department of Biomedical Engineering, Columbia University , New York, New York.
Andrea I Ortuño1 Department of Biomedical Engineering, Columbia University , New York, New York.
David F Meaney2 Department of Bioengineering, University of Pennsylvania , Philadelphia, Pennsylvania.
Cameron R 'Dale' Bass3 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Barclay Morrison1 Department of Biomedical Engineering, Columbia University , New York, New York.
Columbia University · USDuke University · USUniversity of Pennsylvania · US

Funding

Mechanisms of remodeling circuit connectivity after traumatic brain injuryR01NS088176 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI MEANEY, DAVID F · 2015 to 2018
$1.4M
NINDS NIH HHS R01 NS088176
6 · The paper itself

Abstract

Up to 80% of injuries sustained by U.S. soldiers in Operation Enduring Freedom and Operation Iraqi Freedom were the result of blast exposure from improvised explosive devices. Some soldiers experience multiple blasts while on duty, and it has been suggested that symptoms of repetitive blast are similar to those that follow multiple non-blast concussions, such as sport-related concussion. Despite the interest in the effects of repetitive blast exposure, it remains unknown whether an initial blast renders the brain more vulnerable to subsequent exposure, resulting in a synergistic injury response. To investigate the effect of multiple primary blasts on the brain, organotypic hippocampal slice cultures were exposed to single or repetitive (two or three total) primary blasts of varying intensities. Long-term potentiation was significantly reduced following two Level 2 (92.7 kPa, 1.4 msec, 38.5 kPa·msec) blasts delivered 24 h apart without altering basal evoked response. This deficit persisted when the interval between injuries was increased to 72 h but not when the interval was extended to 144 h. The repeated blast exposure with a 24 h interval increased microglia staining and activation significantly but did not significantly increase cell death or damage axons, dendrites, or principal cell layers. Lack of overt structural damage and change in basal stimulated neuron response suggest that injury from repetitive primary blast exposure may specifically affect long-term potentiation. Our studies suggest repetitive primary blasts can exacerbate injury dependent on the injury severity and interval between exposures.

Indexed as

AnimalsBlast InjuriesHippocampusLong-Term PotentiationOrgan Culture TechniquesRatsRats, Sprague-Dawleyblastbrainglia neuronplasticity

Identifiers

PMID26699926
PMCPMC6445278
OpenAlexW2303092219

What OpenQuestion holds

Textmetadata
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.