Evidence map›Paper›PMID 11069968›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2000

Loss of presynaptic and postsynaptic structures is accompanied by compensatory increase in action potential-dependent synaptic input to layer V neocortical pyramidal neurons in aged rats.

T P Wong, G Marchese, M A Casu, A Ribeiro-da-Silva, A C Cuello, Y De Koninck

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

25 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Altered Electrophysiology and Transcriptome of GnRH Neurons in Middle-Aged Female Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  12. Prefrontal cortical GABAergic dysfunction contributes to age-related working memory impairment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  13. Review
  14. Differential balance of prefrontal synaptic activity in successful versus unsuccessful cognitive aging.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  15. Article
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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

6 authors at 1 institution in 2 countries.

T P WongDepartment of Pharmacology and Therapeutics, McGill University, Montreal, Quebec, Canada, H3G 1Y6.
G Marchese
M A Casu
A Ribeiro-da-Silva
A C Cuello
Y De Koninck
Therapeutics Clinical Research · US

Funding

INHIBITORY MECHANISMS IN THE SPINAL DORSAL HORNR01NS034022 · NINDS · MCGILL UNIVERSITY · PI DE KONINCK, YVES · 1996 to 1998
–
NINDS NIH HHS NS-34022
6 · The paper itself

Abstract

Reduction in both presynaptic and postsynaptic structures in the aging neocortex may significantly affect functional synaptic properties in this area. To directly address this issue, we combined whole-cell patch-clamp recording of spontaneously occurring postsynaptic currents (PSCs) with morphological analysis of layer V pyramidal neurons in the parietal cortex of young adult (1- to 2-month-old) and aged (28- to 37-month-old) BN x F344 F(1) hybrid rats. Analysis of spontaneous PSCs was used to contrast functional properties of basal synaptic input with structural alterations in the dendritic tree of pyramidal neurons and density of terminals in contact with these cells. We observed significant changes in a number of morphological parameters of pyramidal neurons in aged rats. These include smaller cell body size and fewer basal dendritic branches (but not of oblique dendrites and dendritic tufts) and spines. Ultrastructural analysis also revealed a lower density of presynaptic terminals per unit length of postsynaptic membrane of labeled pyramidal neurons in the aged brain. This reduction in both presynaptic and postsynaptic elements was paralleled by a significant decrease in frequency of tetrodotoxin-insensitive miniature (action potential-independent) PSCs (mPSCs). The frequency of excitatory and inhibitory mPSCs was reduced to the same extent. In contrast, no significant change was observed in the frequency of spontaneous PSCs recorded in absence of tetrodotoxin (sPSCs), indicating an increase in action potential-dependent (frequency(sPSCs) - frequency(mPSCs)) input to pyramidal neurons in the aged group. This functional compensation may explain the lack of drastic loss of spontaneous neuronal activity in normal aging.

Indexed as

Action PotentialsAgingAnimalsCell CountDendritesExcitatory Postsynaptic PotentialsIn Vitro TechniquesNeocortexParietal LobePatch-Clamp TechniquesPyramidal CellsRatsRats, Inbred BNRats, Inbred F344Synapses

Identifiers

PMID11069968
PMCPMC6773180
OpenAlexW2159633226

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.