Evidence map›Paper›PMID 31055644›Full record

ArticleCellular and molecular life sciences : CMLS2019

Cancellation of nerve excitation by the reversal of nanosecond stimulus polarity and its relevance to the gating time of sodium channels.

Maura Casciola, Shu Xiao, Francesca Apollonio, Alessandra Paffi, Micaela Liberti, Claudia Muratori, Andrei G Pakhomov

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  4. Modulating CaBiophysical journal · 2024
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  10. HumanFrontiers in physiology · 2022
    Article
  11. Article
  12. Article
  13. 2-ns Electrostimulation of CaBiophysical journal · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Excitation and electroporation by MHz bursts of nanosecond stimuli.Biochemical and biophysical research communications · 2019
    Article
  20. 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

7 authors at 2 institutions in 2 countries.

Maura CasciolaFrank Reidy Research Center for Bioelectrics, Old Dominion University, 4211 Monarch Way, Suite 300, Norfolk, VA, 23508, USA.
Shu XiaoFrank Reidy Research Center for Bioelectrics, Old Dominion University, 4211 Monarch Way, Suite 300, Norfolk, VA, 23508, USA.
Francesca ApollonioDepartment of Information Engineering, Electronics and Telecommunications (D.I.E.T.), Sapienza University of Rome, Rome, Italy.
Alessandra PaffiDepartment of Information Engineering, Electronics and Telecommunications (D.I.E.T.), Sapienza University of Rome, Rome, Italy.
Micaela LibertiDepartment of Information Engineering, Electronics and Telecommunications (D.I.E.T.), Sapienza University of Rome, Rome, Italy.
Claudia MuratoriFrank Reidy Research Center for Bioelectrics, Old Dominion University, 4211 Monarch Way, Suite 300, Norfolk, VA, 23508, USA.
Andrei G PakhomovFrank Reidy Research Center for Bioelectrics, Old Dominion University, 4211 Monarch Way, Suite 300, Norfolk, VA, 23508, USA. 2andrei@pakhomov.net.ORCID http://orcid.org/0000-0003-3816-3860
Old Dominion University · USSapienza University of Rome · IT

Funding

Air Force Office of Scientific Research FA9550-15-1-0517Pulse Biosciences 500226-014
6 · The paper itself

Abstract

The initiation of action potentials (APs) by membrane depolarization occurs after a brief vulnerability period, during which excitation can be abolished by the reversal of the stimulus polarity. This vulnerability period is determined by the time needed for gating of voltage-gated sodium channels (VGSC). We compared nerve excitation by ultra-short uni- and bipolar stimuli to define the time frame of bipolar cancellation and of AP initiation. Propagating APs in isolated frog sciatic nerve were elicited by cathodic pulses (200 ns-300 µs), followed by an anodic (canceling) pulse of the same duration after a 0-200-µs delay. We found that the earliest and the latest boundaries for opening the critical number of VGSC needed to initiate AP are, respectively, between 11 and 20 µs and between 100 and 200 µs after the onset of depolarization. Stronger depolarization accelerated AP initiation, apparently due to faster VGSC opening, but not beyond the 11-µs limit. Bipolar cancellation was augmented by reducing pulse duration, shortening the delay between pulses, decreasing the amplitude of the cathodic pulse, and increasing the amplitude of the anodic one. Some of these characteristics contrasted the bipolar cancellation of cell membrane electroporation (Pakhomov et al. in Bioelectrochemistry 122:123-133, 2018; Gianulis et al. in Bioelectrochemistry 119:10-19, 2017), suggesting different mechanisms. The ratio of nerve excitation thresholds for a unipolar cathodic pulse and a symmetrical bipolar pulse increased as a power function as the pulse duration decreased, in remarkable agreement with the predictions of SENN model of nerve excitation (Reilly and Diamant in Health Phys 83(3):356-365, 2002).

Indexed as

Action PotentialsAnimalsAnuraCell MembraneCell Membrane PermeabilityElectroporationFemaleIon Channel GatingNervous SystemSodium ChannelsSodium ChannelsElectropermeabilizationElectroporationGatingNanosecond pulsesnsEPSodium channels

Identifiers

PMID31055644
PMCPMC11105181
OpenAlexW2944561076

What Socratic 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 Socratic graph.