Evidence map›Paper›PMID 30389966›Full record

ArticleScientific reports2018

Fast confocal fluorescence imaging in freely behaving mice.

Clara Dussaux, Vivien Szabo, Yan Chastagnier, Jozsua Fodor, Jean-François Léger, Laurent Bourdieu, Julie Perroy, Cathie Ventalon

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Integrating Optics and Parametrically-Resonant Micro-Scanner Design for Large Working Distance Implantable Microscopy.IEEE/ASME transactions on mechatronics : a joint publication of the IEEE Industrial Electronics Society and the ASME Dynamic Systems and Control Division · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Advances of optical miniscopes forFrontiers in neuroscience · 2022
    Review
  11. Review
  12. Two-Photon Fluorescence Imaging.Advances in experimental medicine and biology · 2021
    Article
  13. Review
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

8 authors at 1 institution in 1 country.

Clara DussauxInstitut de biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, PSL Research University, 46 rue d'Ulm, Paris, 75005, France.
Vivien SzaboIGF, Univ. Montpellier, CNRS, INSERM, 141 rue de la Cardonille, Montpellier, 34094, France.ORCID http://orcid.org/0000-0002-0079-7596
Yan ChastagnierIGF, Univ. Montpellier, CNRS, INSERM, 141 rue de la Cardonille, Montpellier, 34094, France.
Jozsua FodorInstitut de biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, PSL Research University, 46 rue d'Ulm, Paris, 75005, France.
Jean-François LégerInstitut de biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, PSL Research University, 46 rue d'Ulm, Paris, 75005, France.
Laurent BourdieuInstitut de biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, PSL Research University, 46 rue d'Ulm, Paris, 75005, France.ORCID http://orcid.org/0000-0003-0195-8758
Julie PerroyIGF, Univ. Montpellier, CNRS, INSERM, 141 rue de la Cardonille, Montpellier, 34094, France.
Cathie VentalonInstitut de biologie de l'École Normale Supérieure (IBENS), École Normale Supérieure, CNRS, INSERM, PSL Research University, 46 rue d'Ulm, Paris, 75005, France. cathie.ventalon@ens.fr.ORCID http://orcid.org/0000-0001-8174-7840
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence imaging in the brain of freely behaving mice is challenging due to severe miniaturization constraints. In particular, the ability to image a large field of view at high temporal resolution and with efficient out-of-focus background rejection still raises technical difficulties. Here, we present a novel fiberscope system that provides fast (up to 200 Hz) background-free fluorescence imaging in freely behaving mice over a field of view of diameter 230 μm. The fiberscope is composed of a custom-made multipoint-scanning confocal microscope coupled to the animal with an image guide and a micro-objective. By simultaneously registering a multipoint-scanning confocal image and a conventional widefield image, we subtracted the residual out-of-focus background and provided a background-free confocal image. Illumination and detection pinholes were created using a digital micromirror device, providing high adaptability to the sample structure and imaging conditions. Using this novel imaging tool, we demonstrated fast fluorescence imaging of microvasculature up to 120 μm deep in the mouse cortex, with an out-of-focus background reduced by two orders of magnitude compared with widefield microscopy. Taking advantage of the high acquisition rate (200 Hz), we measured red blood cell velocity in the cortical microvasculature and showed an increase in awake, unrestrained mice compared with anaesthetized animals.

Indexed as

AnimalsBlood Flow VelocityCerebral CortexErythrocytesFiber Optic TechnologyIntravital MicroscopyLasersMaleMiceMice, Inbred C57BLMicroscopy, ConfocalMicroscopy, FluorescenceMicrotechnologyMicrovesselsModels, AnimalOptical Fibers

Identifiers

PMID30389966
PMCPMC6214968
OpenAlexW2899188187

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.