Evidence map›Paper›PMID 28840469›Full record

ArticleMolecular neurobiology2018

Early Exposure to Ketamine Impairs Axonal Pruning in Developing Mouse Hippocampus.

Aleksandar Lj Obradovic, Navya Atluri, Lorenza Dalla Massara, Azra Oklopcic, Nikola S Todorovic, Gaurav Katta, Hari P Osuru, Vesna Jevtovic-Todorovic

Open access · greenAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  6. Controversies in anesthesia-induced developmental neurotoxicity.Best practice & research. Clinical anaesthesiology · 2023
    Review
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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

8 authors at 6 institutions in 2 countries.

Aleksandar Lj ObradovicDepartment of Neuroscience, Mount Sinai School of Medicine, New York, NY, USA.
Navya AtluriDepartment of Anesthesiology, University of Colorado School of Medicine, 12401 East 17th Avenue, Aurora, CO, 80045, USA.
Lorenza Dalla MassaraDepartment of Anesthesiology and Pharmacology, University of Padua, Padua, Italy.
Azra OklopcicDepartment of Medicine, University of Virginia Health System, Charlottesville, VA, USA.
Nikola S TodorovicUniversity of Virginia College of Arts and Sciences, Charlottesville, VA, USA.
Gaurav KattaDepartment of Anesthesiology, University of Michigan, Ann Arbor, MI, USA.
Hari P OsuruDepartment of Anesthesiology, University of Colorado School of Medicine, 12401 East 17th Avenue, Aurora, CO, 80045, USA.
Vesna Jevtovic-TodorovicDepartment of Anesthesiology, University of Colorado School of Medicine, 12401 East 17th Avenue, Aurora, CO, 80045, USA. vesna.jevtovic-todorovic@ucdenver.edu.
University of Colorado Denver · USIcahn School of Medicine at Mount Sinai · USUniversity of Michigan–Ann Arbor · USUniversity of Padua · ITUniversity of Virginia Health System · USVirginia College · US

Funding

Anesthesia-induced developmental neurodegenerationR01HD044517 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI JEVTOVIC-TODOROVIC, VESNA · 2005 to 2014
$3.0M
FVMPE-RS Riser System for in vivo and in vitro imaging on anesthesia-induced developmental neurotoxicityR01GM118197 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI JEVTOVIC-TODOROVIC, VESNA · 2016 to 2019
$1.7M
Anesthesia impairs developmental axon pruning and functional neuronal networksR21HD080281 · NICHD · UNIVERSITY OF VIRGINIA · PI JEVTOVIC-TODOROVIC, VESNA · 2015 to 2016
$428k
NICHD NIH HHS R01 HD044517NICHD NIH HHS R21 HD080281NIGMS NIH HHS R01 GM118197
6 · The paper itself

Abstract

Mounting evidence suggests that prolonged exposure to general anesthesia (GA) during brain synaptogenesis damages the immature neurons and results in long-term neurocognitive impairments. Importantly, synaptogenesis relies on timely axon pruning to select axons that participate in active neural circuit formation. This process is in part dependent on proper homeostasis of neurotrophic factors, in particular brain-derived neurotrophic factor (BDNF). We set out to examine how GA may modulate axon maintenance and pruning and focused on the role of BDNF. We exposed post-natal day (PND)7 mice to ketamine using a well-established dosing regimen known to induce significant developmental neurotoxicity. We performed morphometric analyses of the infrapyramidal bundle (IPB) since IPB is known to undergo intense developmental modeling and as such is commonly used as a well-established model of in vivo pruning in rodents. When IPB remodeling was followed from PND10 until PND65, we noted a delay in axonal pruning in ketamine-treated animals when compared to controls; this impairment coincided with ketamine-induced downregulation in BDNF protein expression and maturation suggesting two conclusions: a surge in BDNF protein expression "signals" intense IPB pruning in control animals and ketamine-induced downregulation of BDNF synthesis and maturation could contribute to impaired IPB pruning. We conclude that the combined effects on BDNF homeostasis and impaired axon pruning may in part explain ketamine-induced impairment of neuronal circuitry formation.

Indexed as

Anesthetics, DissociativeAnimalsAnimals, NewbornAxonsHippocampusKetamineMiceAnesthetics, DissociativeKetamineBrain-derived neurotrophic factorGeneral anesthesiaImmature brainInfrapyramidal bundleMossy fibersSynaptogenesis

Identifiers

PMID28840469
PMCPMC5808855
OpenAlexW2750304547

What OpenQuestion holds

Textmetadata
LicenceTDM
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.