Evidence map›Paper›PMID 27535370›Full record

ArticleJournal of neurophysiology2016

Large-scale recording of thalamocortical circuits: in vivo electrophysiology with the two-dimensional electronic depth control silicon probe.

Richárd Fiáth, Patrícia Beregszászi, Domonkos Horváth, Lucia Wittner, Arno A A Aarts, Patrick Ruther, Hercules P Neves, Hajnalka Bokor, László Acsády, István Ulbert

Abstract 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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Semi-Implantable Bioelectronics.Nano-micro letters · 2022
    Review
  3. Article
  4. Novel electrode technologies for neural recordings.Nature reviews. Neuroscience · 2019
    Review
  5. Article
  6. Frontiers in neuroscience · 2019
    Article
  7. 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

10 authors.

Richárd FiáthGroup of Comparative Psychophysiology, Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Patrícia BeregszásziFaculty of Information Technology and Bionics, Pázmány Péter, Catholic University, Budapest, Hungary.
Domonkos HorváthGroup of Comparative Psychophysiology, Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Lucia WittnerGroup of Comparative Psychophysiology, Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Arno A A AartsATLAS NeuroEngineering, Leuven, Belgium.
Patrick RutherDepartment of Microsystems Engineering (IMTEK), University of Freiburg, Freiburg, Germany.
Hercules P NevesUnitec Semicondutores, Ribeirão das Neves, Brazil.
Hajnalka BokorLaboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
László AcsádyLaboratory of Thalamus Research, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
István UlbertGroup of Comparative Psychophysiology, Institute of Cognitive Neuroscience and Psychology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary; ulbert.istvan@ttk.mta.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recording simultaneous activity of a large number of neurons in distributed neuronal networks is crucial to understand higher order brain functions. We demonstrate the in vivo performance of a recently developed electrophysiological recording system comprising a two-dimensional, multi-shank, high-density silicon probe with integrated complementary metal-oxide semiconductor electronics. The system implements the concept of electronic depth control (EDC), which enables the electronic selection of a limited number of recording sites on each of the probe shafts. This innovative feature of the system permits simultaneous recording of local field potentials (LFP) and single- and multiple-unit activity (SUA and MUA, respectively) from multiple brain sites with high quality and without the actual physical movement of the probe. To evaluate the in vivo recording capabilities of the EDC probe, we recorded LFP, MUA, and SUA in acute experiments from cortical and thalamic brain areas of anesthetized rats and mice. The advantages of large-scale recording with the EDC probe are illustrated by investigating the spatiotemporal dynamics of pharmacologically induced thalamocortical slow-wave activity in rats and by the two-dimensional tonotopic mapping of the auditory thalamus. In mice, spatial distribution of thalamic responses to optogenetic stimulation of the neocortex was examined. Utilizing the benefits of the EDC system may result in a higher yield of useful data from a single experiment compared with traditional passive multielectrode arrays, and thus in the reduction of animals needed for a research study.

Indexed as

Electrodes, ImplantedSiliconAcoustic StimulationAction PotentialsAnimalsCerebral CortexFemaleMaleMiceMice, TransgenicNerve NetOptogeneticsRatsRats, WistarThalamusSiliconelectronic depth controlhigh-density recordingoptogeneticssilicon probethalamocortical oscillation

Identifiers

PMID27535370
PMCPMC5110634

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Read underepoch 390

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.