Evidence map›Paper›PMID 27812002›Full record

ArticleScientific reports2016

On-chip, multisite extracellular and intracellular recordings from primary cultured skeletal myotubes.

Noha Rabieh, Silviya M Ojovan, Nava Shmoel, Hadas Erez, Eilon Maydan, Micha E Spira

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 38 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 1 institution in 1 country.

Noha RabiehDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Silviya M OjovanDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Nava ShmoelDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Hadas ErezDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Eilon MaydanDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Micha E SpiraDepartment of Neurobiology, the Alexander Silberman Institute of Life Science. The C. Smith Family and Prof. J. Elkes Laboratory for Collaborative Research in Psychobiology and the Harvey M. Kruger Family Center for Nanoscience. The Hebrew University of Jerusalem, Edmond J. Safra Campus, Jerusalem, 91904, Israel.
Hebrew University of Jerusalem · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In contrast to the extensive use of microelectrode array (MEA) technology in electrophysiological studies of cultured neurons and cardiac muscles, the vast field of skeletal muscle research has yet to adopt the technology. Here we demonstrate an empowering MEA technology for high quality, multisite, long-term electrophysiological recordings from cultured skeletal myotubes. Individual rat skeletal myotubes cultured on micrometer sized gold mushroom-shaped microelectrode (gMμE) based MEA tightly engulf the gMμEs, forming a high seal resistance between the myotubes and the gMμEs. As a consequence, spontaneous action potentials generated by the contracting myotubes are recorded as extracellular field potentials with amplitudes of up to 10 mV for over 14 days. Application of a 10 ms, 0.5-0.9 V voltage pulse through the gMμEs electroporated the myotube membrane, and transiently converted the extracellular to intracellular recording mode for 10-30 min. In a fraction of the cultures stable attenuated intracellular recordings were spontaneously produced. In these cases or after electroporation, subthreshold spontaneous potentials were also recorded. The introduction of the gMμE-MEA as a simple-to-use, high-quality electrophysiological tool together with the progress made in the use of cultured human myotubes opens up new venues for basic and clinical skeletal muscle research, preclinical drug screening, and personalized medicine.

Indexed as

Action PotentialsAnimalsCells, CulturedElectroporationHumansMicroelectrodesMuscle Fibers, SkeletalMuscle, SkeletalNeuronsRats

Identifiers

PMID27812002
PMCPMC5095645
OpenAlexW2546993894

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.