Evidence map›Paper›PMID 24133226›Full record

ArticleJournal of neurophysiology2014

Characterization of age-related changes in synaptic transmission onto F344 rat basal forebrain cholinergic neurons using a reduced synaptic preparation.

William H Griffith, Dustin W Dubois, Annette Fincher, Kathryn A Peebles, Jennifer L Bizon, David Murchison

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. 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
    Article
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  8. Article
  9. Article
  10. Review
  11. Structural and Functional Synaptic Plasticity Induced by Convergent Synapse Loss in theThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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 2 institutions in 1 country.

William H GriffithDepartment of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M Health Science Center, Bryan, Texas; and.
Dustin W Dubois
Annette Fincher
Kathryn A Peebles
Jennifer L Bizon
David Murchison
Texas A&M Health Science Center · USUniversity of Florida · US

Funding

Neural Mechanisms of Cognitive Decline in AgingR01AG029421 · NIA · UNIVERSITY OF FLORIDA · PI BIZON, JENNIFER LYNN · 2007 to 2018
$3.1M
PHYSIOLOGY OF CHOLINERGIC BASAL FOREBRAIN NEURONSR01AG007805 · NIA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GRIFFITH, WILLIAM H · 1989 to 2007
$1.6M
Estrogens, Ovarian Aging and Calcium Channel ModulationR01AG041360 · NIA · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI GRIFFITH, WILLIAM H · 2011 to 2015
$1.4M
NIA NIH HHS AG007805NIA NIH HHS AG029421NIA NIH HHS AG041360NIA NIH HHS R01 AG007805
6 · The paper itself

Abstract

Basal forebrain (BF) cholinergic neurons participate in a number of cognitive processes that become impaired during aging. We previously found that age-related enhancement of Ca(2+) buffering in rat cholinergic BF neurons was associated with impaired performance in the water maze spatial learning task (Murchison D, McDermott AN, Lasarge CL, Peebles KA, Bizon JL, and Griffith WH. J Neurophysiol 102: 2194-2207, 2009). One way that altered Ca(2+) buffering could contribute to cognitive impairment involves synaptic function. In this report we show that synaptic transmission in the BF is altered with age and cognitive status. We have examined the properties of spontaneous postsynaptic currents (sPSCs) in cholinergic BF neurons that have been mechanically dissociated without enzymes from behaviorally characterized F344 rats. These isolated neurons retain functional presynaptic terminals on their somata and proximal dendrites. Using whole cell patch-clamp recording, we show that sPSCs and miniature PSCs are predominately GABAergic (bicuculline sensitive) and in all ways closely resemble PSCs recorded in a BF in vitro slice preparation. Adult (4-7 mo) and aged (22-24 mo) male rats were cognitively assessed using the water maze. Neuronal phenotype was identified post hoc using single-cell RT-PCR. The frequency of sPSCs was reduced during aging, and this was most pronounced in cognitively impaired subjects. This is the same population that demonstrated increased intracellular Ca(2+) buffering. We also show that increasing Ca(2+) buffering in the synaptic terminals of young BF neurons can mimic the reduced frequency of sPSCs observed in aged BF neurons.

Indexed as

Miniature Postsynaptic PotentialsAge FactorsAnimalsCalciumCholinergic Neuronsgamma-Aminobutyric AcidMaleMaze LearningProsencephalonRatsRats, Inbred F344SynapsesCalciumgamma-Aminobutyric Acidagingbasal forebrainbehaviorGABAsynaptic transmission

Identifiers

PMID24133226
PMCPMC3921388
OpenAlexW2317954848

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.