Evidence map›Paper›PMID 26864767›Full record

ArticleJournal of neurophysiology2016

Precaution for volume conduction in rodent cortical electroencephalography using high-density polyimide-based microelectrode arrays on the skull.

P J Stienen, M Venzi, W Poppendieck, K P Hoffmann, E Åberg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 3 institutions in 2 countries.

P J StienenAstraZeneca Research and Development, Innovative Medicines and Early Development, Personalized Healthcare and Biomarkers, AstraZeneca Translational Science Centre at Science for Life Laboratory, Solna, Sweden; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; and pjstienen@gmail.com.
M VenziAstraZeneca Research and Development, Innovative Medicines and Early Development, Personalized Healthcare and Biomarkers, AstraZeneca Translational Science Centre at Science for Life Laboratory, Solna, Sweden; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; and.
W PoppendieckDepartment of Medical Engineering and Neuroprosthetics, Fraunhofer Institute for Biomedical Engineering, St. Ingbert, Germany.
K P HoffmannDepartment of Medical Engineering and Neuroprosthetics, Fraunhofer Institute for Biomedical Engineering, St. Ingbert, Germany.
E ÅbergAstraZeneca Research and Development, Innovative Medicines and Early Development, Personalized Healthcare and Biomarkers, AstraZeneca Translational Science Centre at Science for Life Laboratory, Solna, Sweden; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; and.
AstraZeneca (Sweden) · SEFraunhofer Institute for Biomedical Engineering · DEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In humans, significant progress has been made to link spatial changes in electroencephalographic (EEG) spectral density, connectivity strength, and phase-amplitude modulation to neurological, physiological, and psychological correlates. In contrast, standard rodent EEG techniques employ only few electrodes, which results in poor spatial resolution. Recently, a technique was developed to overcome this limitation in mice. This technique was based on a polyimide-based microelectrode (PBM) array applied on the mouse skull, maintaining a significant number of electrodes with consistent contact, electrode impedance, and mechanical stability. The present study built on this technique by extending it to rats. Therefore, a similar PBM array, but adapted to rats, was designed and fabricated. In addition, this array was connected to a wireless EEG headstage, allowing recording in untethered, freely moving rats. The advantage of a high-density array relies on the assumption that the signal recorded from the different electrodes is generated from distinct sources, i.e., not volume-conducted. Therefore, the utility and validity of the array were evaluated by determining the level of synchrony between channels due to true synchrony or volume conduction during basal vigilance states and following a subanesthetic dose of ketamine. Although the PBM array allowed recording with high signal quality, under both drug and drug-free conditions, high synchronization existed due to volume conduction between the electrodes even in the higher spectral frequency range. Discrimination existed only between frontally and centrally/distally grouped electrode pairs. Therefore, caution should be used in interpreting spatial data obtained from high-density PBM arrays in rodents.

Indexed as

Neural ConductionAnimalsCerebral CortexElectroencephalographyMaleMicroelectrodesRatsResins, Syntheticpolyimide resinResins, Syntheticgammahigh-density EEGketaminetheta

Identifiers

PMID26864767
PMCPMC4869495
OpenAlexW2253037029

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.