Evidence map›Paper›PMID 24386417›Full record

ArticlePloS one2013

Decreased response to acetylcholine during aging of aplysia neuron R15.

Komolitdin Akhmedov, Valerio Rizzo, Beena M Kadakkuzha, Christopher J Carter, Neil S Magoski, Thomas R Capo, Sathyanarayanan V Puthanveettil

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Komolitdin AkhmedovDepartment of Neuroscience, The Scripps Research Institute, Scripps Florida, Jupiter, Florida, United States of America.
Valerio RizzoDepartment of Neuroscience, The Scripps Research Institute, Scripps Florida, Jupiter, Florida, United States of America.
Beena M KadakkuzhaDepartment of Neuroscience, The Scripps Research Institute, Scripps Florida, Jupiter, Florida, United States of America.
Christopher J CarterDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.
Neil S MagoskiDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.
Thomas R CapoDivision of Marine Biology and Fisheries, University of Miami Rosenstiel School of Marine and Atmospheric Science, Miami, Florida, United States of America.
Sathyanarayanan V PuthanveettilDepartment of Neuroscience, The Scripps Research Institute, Scripps Florida, Jupiter, Florida, United States of America.
Scripps Research Institute · USQueen's University · CAUniversity of Miami · US

Funding

The National Resource for Aplysia-Curation & Informatics.P40OD010952 · OD · UNIVERSITY OF MIAMI ROSENTEIL SCHOOL · PI M Danielle McDonald · 2012 to 2026
$10.7M
NIH HHS P40 OD010952
6 · The paper itself

Abstract

How aging affects the communication between neurons is poorly understood. To address this question, we have studied the electrophysiological properties of identified neuron R15 of the marine mollusk Aplysia californica. R15 is a bursting neuron in the abdominal ganglia of the central nervous system and is implicated in reproduction, water balance, and heart function. Exposure to acetylcholine (ACh) causes an increase in R15 burst firing. Whole-cell recordings of R15 in the intact ganglia dissected from mature and old Aplysia showed specific changes in burst firing and properties of action potentials induced by ACh. We found that while there were no significant changes in resting membrane potential and latency in response to ACh, the burst number and burst duration is altered during aging. The action potential waveform analysis showed that unlike mature neurons, the duration of depolarization and the repolarization amplitude and duration did not change in old neurons in response to ACh. Furthermore, single neuron quantitative analysis of acetylcholine receptors (AChRs) suggested alteration of expression of specific AChRs in R15 neurons during aging. These results suggest a defect in cholinergic transmission during aging of the R15 neuron.

Indexed as

AcetylcholineAnimalsAplysiaBase SequenceCellular SenescenceCholinergic AgonistsMolecular Sequence DataNeuronsReceptors, CholinergicAcetylcholineCholinergic AgonistsReceptors, Cholinergic

Identifiers

PMID24386417
PMCPMC3874043
OpenAlexW2031044812

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.