Evidence map›Paper›PMID 27167092›Full record

ArticleJournal of visualized experiments : JoVE2016

The c-FOS Protein Immunohistological Detection: A Useful Tool As a Marker of Central Pathways Involved in Specific Physiological Responses In Vivo and Ex Vivo.

Anne-Sophie Perrin-Terrin, Florine Jeton, Aurelien Pichon, Alain Frugière, Jean-Paul Richalet, Laurence Bodineau, Nicolas Voituron

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

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  10. Whole-brain analysis of CObioRxiv : the preprint server for biology · 2023
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  15. Review
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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

7 authors at 3 institutions in 1 country.

Anne-Sophie Perrin-TerrinSorbonne Paris Cité, Laboratory "Hypoxia & Lung" EA2363, University Paris 13; UPMC Univ Paris 06, INSERM, UMR_S1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Universités.
Florine JetonSorbonne Paris Cité, Laboratory "Hypoxia & Lung" EA2363, University Paris 13; Laboratory of Excellence GR-Ex.
Aurelien PichonSorbonne Paris Cité, Laboratory "Hypoxia & Lung" EA2363, University Paris 13; Laboratory of Excellence GR-Ex; Laboratory MOVE (EA 6314), University of Poitiers.
Alain FrugièreUPMC Univ Paris 06, INSERM, UMR_S1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Universités.
Jean-Paul RichaletSorbonne Paris Cité, Laboratory "Hypoxia & Lung" EA2363, University Paris 13; Laboratory of Excellence GR-Ex.
Laurence BodineauUPMC Univ Paris 06, INSERM, UMR_S1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Universités.
Nicolas VoituronSorbonne Paris Cité, Laboratory "Hypoxia & Lung" EA2363, University Paris 13; Laboratory of Excellence GR-Ex; nicolas.voituron@univ-paris13.fr.
Inserm · FRSorbonne Université · FRUniversité Sorbonne Paris Nord · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many studies seek to identify and map the brain regions involved in specific physiological regulations. The proto-oncogene c-fos, an immediate early gene, is expressed in neurons in response to various stimuli. The protein product can be readily detected with immunohistochemical techniques leading to the use of c-FOS detection to map groups of neurons that display changes in their activity. In this article, we focused on the identification of brainstem neuronal populations involved in the ventilatory adaptation to hypoxia or hypercapnia. Two approaches were described to identify involved neuronal populations in vivo in animals and ex vivo in deafferented brainstem preparations. In vivo, animals were exposed to hypercapnic or hypoxic gas mixtures. Ex vivo, deafferented preparations were superfused with hypoxic or hypercapnic artificial cerebrospinal fluid. In both cases, either control in vivo animals or ex vivo preparations were maintained under normoxic and normocapnic conditions. The comparison of these two approaches allows the determination of the origin of the neuronal activation i.e., peripheral and/or central. In vivo and ex vivo, brainstems were collected, fixed, and sliced into sections. Once sections were prepared, immunohistochemical detection of the c-FOS protein was made in order to identify the brainstem groups of cells activated by hypoxic or hypercapnic stimulations. Labeled cells were counted in brainstem respiratory structures. In comparison to the control condition, hypoxia or hypercapnia increased the number of c-FOS labeled cells in several specific brainstem sites that are thus constitutive of the neuronal pathways involved in the adaptation of the central respiratory drive.

Indexed as

AnimalsBiomarkersBrain StemImmunohistochemistryMiceMice, Inbred C57BLNeuronsProto-Oncogene Proteins c-fosRatsRats, Sprague-DawleyBiomarkersProto-Oncogene Proteins c-fos

Identifiers

PMID27167092
PMCPMC4941991
OpenAlexW2344175872

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.