Evidence map›Paper›PMID 24808928›Full record

ArticleCognitive neurodynamics2014

An ephaptic transmission model of CA3 pyramidal cells: an investigation into electric field effects.

Xile Wei, Yinhong Chen, Meili Lu, Bin Deng, Haitao Yu, Jiang Wang, Yanqiu Che, Chunxiao Han

Open access · bronzeAbstract read
In one paragraph

Article in Cognitive neurodynamics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 7 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

8 authors at 2 institutions in 1 country.

Xile WeiSchool of Electrical Engineering and Automation, Tianjin University, Tianjin, 300072 China.
Yinhong ChenSchool of Electrical Engineering and Automation, Tianjin University, Tianjin, 300072 China.
Meili LuSchool of Informational Technology and Engineering, Tianjin University of Technology and Education, Tianjin, 300222 China.
Bin DengSchool of Electrical Engineering and Automation, Tianjin University, Tianjin, 300072 China.
Haitao YuSchool of Electrical Engineering and Automation, Tianjin University, Tianjin, 300072 China.
Jiang WangSchool of Electrical Engineering and Automation, Tianjin University, Tianjin, 300072 China.
Yanqiu CheSchool of Automation and Electrical Engineering, Tianjin University of Technology and Education, Tianjin, 300222 China.
Chunxiao HanSchool of Automation and Electrical Engineering, Tianjin University of Technology and Education, Tianjin, 300222 China.
Tianjin University · CNTianjin University of Technology and Education · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular electric fields existing throughout the living brain affect the neural coding and information processing via ephaptic transmission, independent of synapses. A two-compartment whole field effect model (WFEM) of pyramidal neurons embedded within a resistive array which simulates the extracellular medium i.e. ephapse is developed to study the effects of electric field on neuronal behaviors. We derive the two linearized filed effect models (LFEM-1 and LFEM-2) from WFEM at the stable resting state. Through matching these simplified models to the subthreshold membrane response in experiments of the resting pyramidal cells exposed to applied electric fields, we not only verify our proposed model's validity but also found the key parameters which dominate subthreshold frequency response characteristic. Moreover, we find and give its underlying biophysical mechanism that the unsymmetrical properties of active ion channels results in the very different low-frequency response of somatic and dendritic compartments. Following, WFEM is used to investigate both direct-current (DC) and alternating-current field effect on the neural firing patterns by bifurcation analyses. We present that DC electric field could modulate neuronal excitability, with the positive field improving the excitability, the modest negative field suppressing the excitability, but interestingly, the larger negative field re-exciting the neuron back into spiking behavior. The neuron exposed to the sinusoidal electric field exhibits abundant firing patterns sensitive to the input frequency and intensity. In addition, the electrical properties of ephapse can modulate the efficacy of field effect. Our simulated results are qualitatively in line with the relevant experimental results and can explain some experimental phenomena. Furthermore, they are helpful to provide the predictions which can be tested in future experiments.

Indexed as

Ephaptic transmissionExtracellular electric fieldField effectFiring patternSubthreshold

Identifiers

PMID24808928
PMCPMC4012066
OpenAlexW2079235390

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.