Evidence map›Paper›PMID 26612326›Full record

ArticleScientific reports2015

In Vivo Voltage-Sensitive Dye Imaging of Subcortical Brain Function.

Qinggong Tang, Vassiliy Tsytsarev, Chia-Pin Liang, Fatih Akkentli, Reha S Erzurumlu, Yu Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  8. Neurophotonics · 2020
    Article
  9. Review
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  11. Real-time monitoring of microdistribution of antibody-photon absorber conjugates during photoimmunotherapy in vivo.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  12. Article
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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.

Qinggong TangFischell Department of Bioengineering, University of Maryland, College Park, MD 20742 USA.
Vassiliy TsytsarevFischell Department of Bioengineering, University of Maryland, College Park, MD 20742 USA.
Chia-Pin LiangFischell Department of Bioengineering, University of Maryland, College Park, MD 20742 USA.
Fatih AkkentliDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201 USA.
Reha S ErzurumluDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201 USA.
Yu ChenFischell Department of Bioengineering, University of Maryland, College Park, MD 20742 USA.
University of Maryland, College Park · USUniversity of Maryland, Baltimore · US

Funding

SOMATOSENSORY CORTICAL DEVELOPMENT AND PLASTICITYR01NS039050 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2000 to 2013
$4.6M
Consequences of Developmental Defects in Somatosensory Map formationR01NS084818 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ERZURUMLU, REHA S · 2014 to 2024
$4.2M
NINDS NIH HHS NS039050NINDS NIH HHS NS084818NINDS NIH HHS R01 NS039050NINDS NIH HHS R01 NS084818
6 · The paper itself

Abstract

The whisker system of rodents is an excellent model to study peripherally evoked neural activity in the brain. Discrete neural modules represent each whisker in the somatosensory cortex ("barrels"), thalamus ("barreloids"), and brain stem ("barrelettes"). Stimulation of a single whisker evokes neural activity sequentially in its corresponding barrelette, barreloid, and barrel. Conventional optical imaging of functional activation in the brain is limited to surface structures such as the cerebral cortex. To access subcortical structures and image sensory-evoked neural activity, we designed a needle-based optical system using gradient-index (GRIN) rod lens. We performed voltage-sensitive dye imaging (VSDi) with GRIN rod lens to visualize neural activity evoked in the thalamic barreloids by deflection of whiskers in vivo. We stimulated several whiskers together to determine the sensitivity of our approach in differentiating between different barreloid responses. We also carried out stimulation of different whiskers at different times. Finally, we used muscimol in the barrel cortex to silence the corticothalamic inputs while imaging in the thalamus. Our results show that it is possible to obtain functional maps of the sensory periphery in deep brain structures such as the thalamic barreloids. Our approach can be broadly applicable to functional imaging of other core brain structures.

Indexed as

AnimalsBrain StemColoring AgentsElectric StimulationEvoked Potentials, SomatosensoryFemaleGABA-A Receptor AgonistsInjections, IntraventricularMaleMiceMuscimolSomatosensory CortexStereotaxic TechniquesThalamusVibrissaeVoltage-Sensitive Dye ImagingColoring AgentsGABA-A Receptor AgonistsMuscimol

Identifiers

PMID26612326
PMCPMC4661443
OpenAlexW2411531646

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.