Evidence map›Paper›PMID 23542382›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Increased axonal bouton dynamics in the aging mouse cortex.

Federico W Grillo, Sen Song, Leonor M Teles-Grilo Ruivo, Lieven Huang, Ge Gao, Graham W Knott, Bohumil Maco, Valentina Ferretti, Dawn Thompson, Graham E Little and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

71 citing papers in PubMed.

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  12. Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
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  15. The synapse in traumatic brain injury.Brain : a journal of neurology · 2021
    Review
  16. Article
  17. Article
  18. Article
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  20. Article

11 more citing papers are in PubMed but not listed here.

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

11 authors.

Federico W GrilloMedical Research Council Clinical Science Centre, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Sen Song
Leonor M Teles-Grilo Ruivo
Lieven Huang
Ge Gao
Graham W Knott
Bohumil Maco
Valentina Ferretti
Dawn Thompson
Graham E Little
Vincenzo De Paola

Funding

Medical Research Council MC_U120088464
6 · The paper itself

Abstract

Aging is a major risk factor for many neurological diseases and is associated with mild cognitive decline. Previous studies suggest that aging is accompanied by reduced synapse number and synaptic plasticity in specific brain regions. However, most studies, to date, used either postmortem or ex vivo preparations and lacked key in vivo evidence. Thus, whether neuronal arbors and synaptic structures remain dynamic in the intact aged brain and whether specific synaptic deficits arise during aging remains unknown. Here we used in vivo two-photon imaging and a unique analysis method to rigorously measure and track the size and location of axonal boutons in aged mice. Unexpectedly, the aged cortex shows circuit-specific increased rates of axonal bouton formation, elimination, and destabilization. Compared with the young adult brain, large (i.e., strong) boutons show 10-fold higher rates of destabilization and 20-fold higher turnover in the aged cortex. Size fluctuations of persistent boutons, believed to encode long-term memories, also are larger in the aged brain, whereas bouton size and density are not affected. Our data uncover a striking and unexpected increase in axonal bouton dynamics in the aged cortex. The increased turnover and destabilization rates of large boutons indicate that learning and memory deficits in the aged brain arise not through an inability to form new synapses but rather through decreased synaptic tenacity. Overall our study suggests that increased synaptic structural dynamics in specific cortical circuits may be a mechanism for age-related cognitive decline.

Indexed as

Age FactorsAgingAnimalsAxonsCerebral CortexImage Processing, Computer-AssistedImmunohistochemistryMaleMiceMice, Inbred C57BLMicroscopy, ElectronNeuronal PlasticityPresynaptic Terminals

Identifiers

PMID23542382
PMCPMC3631669

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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.