Evidence map›Paper›PMID 33831000›Full record

ArticlePloS one2021

New methods for quantifying rapidity of action potential onset differentiate neuron types.

Ahmed A Aldohbeyb, Jozsef Vigh, Kevin L Lear

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

3 authors at 2 institutions in 2 countries.

Ahmed A AldohbeybSchool of Biomedical Engineering, Colorado State University, Fort Collins, CO, United States of America.ORCID 0000-0001-8324-1122
Jozsef VighSchool of Biomedical Engineering, Colorado State University, Fort Collins, CO, United States of America.
Kevin L LearSchool of Biomedical Engineering, Colorado State University, Fort Collins, CO, United States of America.
Colorado State University · USKing Saud University · SA

Funding

Opioid Modulation of Retinal Ganglion Cells Providing Photoentrainment of the Circadian ClockR01EY029227 · NEI · COLORADO STATE UNIVERSITY · PI Jozsef Vigh · 2019 to 2026
$2.6M
NEI NIH HHS R01 EY029227
6 · The paper itself

Abstract

Two new methods for quantifying the rapidity of action potential onset have lower relative standard deviations and better distinguish neuron cell types than current methods. Action potentials (APs) in most central mammalian neurons exhibit sharp onset dynamics. The main views explaining such an abrupt onset differ. Some studies suggest sharp onsets reflect cooperative sodium channels activation, while others suggest they reflect AP backpropagation from the axon initial segment. However, AP onset rapidity is defined subjectively in these studies, often using the slope at an arbitrary value on the phase plot. Thus, we proposed more systematic methods using the membrane potential's second-time derivative ([Formula: see text]) peak width. Here, the AP rapidity was measured for four different cortical and hippocampal neuron types using four quantification methods: the inverse of full-width at the half maximum of the [Formula: see text] peak (IFWd2), the inverse of half-width at the half maximum of the [Formula: see text] peak (IHWd2), the phase plot slope, and the error ratio method. The IFWd2 and IHWd2 methods show the smallest variation among neurons of the same type. Furthermore, the AP rapidity, using the [Formula: see text] peak width methods, significantly differentiates between different types of neurons, indicating that AP rapidity can be used to classify neuron types. The AP rapidity measured using the IFWd2 method was able to differentiate between all four neuron types analyzed. Therefore, the [Formula: see text] peak width methods provide another sensitive tool to investigate the mechanisms impacting the AP onset dynamics.

Indexed as

Models, NeurologicalAction PotentialsAxonsHumans

Identifiers

PMID33831000
PMCPMC8032118
OpenAlexW3148919975

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.