Evidence map›Paper›PMID 31323444›Full record

ArticleNeurobiology of aging2019

Reduced sensory-evoked structural plasticity in the aging barrel cortex.

Rebecca L Voglewede, Kaeli M Vandemark, Andrew M Davidson, Annie R DeWitt, Marissa D Heffler, Emma H Trimmer, Ricardo Mostany

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dendritic Spines of Layer 5 Pyramidal Neurons of the Aging Somatosensory Cortex Exhibit Reduced Volumetric Remodeling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
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 1 institution in 1 country.

Rebecca L VoglewedeNeuroscience Program, Tulane University School of Science and Engineering, New Orleans, LA, USA; Tulane Brain Institute, Tulane University, New Orleans, LA, USA; Department of Pharmacology, Tulane University School of Medicine, New Orleans, LA, USA.
Kaeli M VandemarkNeuroscience Program, Tulane University School of Science and Engineering, New Orleans, LA, USA; Tulane Brain Institute, Tulane University, New Orleans, LA, USA.
Andrew M DavidsonDepartment of Pharmacology, Tulane University School of Medicine, New Orleans, LA, USA; Department of Cell and Molecular Biology, Tulane University School of Science and Engineering, New Orleans, LA, USA.
Annie R DeWittNeuroscience Program, Tulane University School of Science and Engineering, New Orleans, LA, USA; Tulane Brain Institute, Tulane University, New Orleans, LA, USA.
Marissa D HefflerNeuroscience Program, Tulane University School of Science and Engineering, New Orleans, LA, USA; Tulane Brain Institute, Tulane University, New Orleans, LA, USA; Department of Biomedical Engineering, Tulane University School of Science and Engineering, Lindy Boggs Center Suite 500, New Orleans, LA, USA.
Emma H TrimmerDepartment of Pharmacology, Tulane University School of Medicine, New Orleans, LA, USA.
Ricardo MostanyNeuroscience Program, Tulane University School of Science and Engineering, New Orleans, LA, USA; Tulane Brain Institute, Tulane University, New Orleans, LA, USA; Department of Pharmacology, Tulane University School of Medicine, New Orleans, LA, USA. Electronic address: rmostany@tulane.edu.
Tulane University · US

Funding

The role of the CMV-associated reactive oxygen species in age-relatedP20GM103629 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI ROUT, NAMITA · 2012 to 2021
$22.4M
Cortical Synaptic Dynamics during Learning in the Aging BrainR01AG047296 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI MOSTANY, RICARDO · 2016 to 2020
$1.7M
NIA NIH HHS R01 AG047296NIGMS NIH HHS P20 GM103629
6 · The paper itself

Abstract

Impairments in synaptic connectivity have been linked to cognitive deficits in age-related neurodegenerative disorders and healthy aging. However, the anatomical and structural bases of these impairments have not been identified yet. A hallmark of neural plasticity in young adults is short-term synaptic rearrangement, yet aged animals already display higher synaptic turnover rates at the baseline. Using two-photon excitation (2PE) microscopy, we explored if this elevated turnover alters the aged brain's response to plasticity. Following a sensory-evoked plasticity protocol involving whisker stimulation, aged mice display reduced spine dynamics (gain, loss, and turnover), decreased spine clustering, and lower spine stability when compared to young adult mice. These results suggest a deficiency of the cortical neurons of aged mice to structurally incorporate new sensory experiences, in the form of clustered, long-lasting synapses, into already existing cortical circuits. This research provides the first evidence linking experience-dependent plasticity with in vivo spine dynamics in the aged brain and supports a model of both reduced synaptic plasticity and reduced synaptic tenacity in the aged somatosensory system.

Indexed as

AgingAnimalsDendritic SpinesMaleMiceMice, TransgenicMicroscopy, Fluorescence, MultiphotonNeurodegenerative DiseasesNeuroimagingNeuronal PlasticitySomatosensory CortexSynapsesVibrissaeAgingClusteringDendritic spinePrimary somatosensory cortexStructural plasticityTwo-photon imaging

Identifiers

PMID31323444
PMCPMC6732242
OpenAlexW2953921957

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.