Evidence map›Paper›PMID 25811836›Full record

ArticlePloS one2015

Weak sinusoidal electric fields entrain spontaneous Ca transients in the dendritic tufts of CA1 pyramidal cells in rat hippocampal slice preparations.

Kazuma Maeda, Ryuichi Maruyama, Toru Nagae, Masashi Inoue, Toru Aonishi, Hiroyoshi Miyakawa

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-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

4 citing papers in PubMed, 14 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

6 authors at 2 institutions in 1 country.

Kazuma MaedaLaboratory of Cellular Neurobiology, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
Ryuichi MaruyamaDepartment of Computational Intelligence and System Science, Tokyo Institute of Technology, Midori-ku, Kanagawa, Japan.
Toru NagaeLaboratory of Cellular Neurobiology, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
Masashi InoueLaboratory of Cellular Neurobiology, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
Toru AonishiDepartment of Computational Intelligence and System Science, Tokyo Institute of Technology, Midori-ku, Kanagawa, Japan.
Hiroyoshi MiyakawaLaboratory of Cellular Neurobiology, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
Tokyo University of Pharmacy and Life Sciences · JPTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons might interact via electric fields and this notion has been referred to as ephaptic interaction. It has been shown that various types of ion channels are distributed along the dendrites and are capable of supporting generation of dendritic spikes. We hypothesized that generation of dendritic spikes play important roles in the ephaptic interactions either by amplifying the impact of electric fields or by providing current source to generate electric fields. To test if dendritic activities can be modulated by electric fields, we developed a method to monitor local Ca-transients in the dendrites of a neuronal population in acute rat hippocampal slices by applying spinning-disk confocal microscopy and multi-cell dye loading technique. In a condition in which the dendrites of CA1 pyramidal neurons show spontaneous Ca-transients due to added 50 μM 4-aminopyridine to the bathing medium and adjusted extracellular potassium concentration, we examined the impact of sinusoidal electric fields on the Ca-transients. We have found that spontaneously occurring fast-Ca-transients in the tufts of the apical dendrites of CA1 pyramidal neurons can be blocked by applying 1 μM tetrodotoxin, and that the timing of the transients become entrained to sub-threshold 1-4 Hz electric fields with an intensity as weak as 0.84 mV/mm applied parallel to the somato-dendritic axis of the neurons. The extent of entrainment increases with intensity below 5 mV/mm, but does not increase further over the range of 5-20 mV/mm. These results suggest that population of pyramidal cells might be able to detect electric fields with biologically relevant intensity by modulating the timing of dendritic spikes.

Indexed as

AnimalsCalciumDendritesElectric StimulationHippocampusMaleMembrane PotentialsPyramidal CellsRatsCalcium

Identifiers

PMID25811836
PMCPMC4374834
OpenAlexW2094299540

What OpenQuestion holds

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Registered trials

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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.