Evidence map›Paper›PMID 25309435›Full record

ArticleFrontiers in aging neuroscience2014

Astrocytosis in parkinsonism: considering tripartite striatal synapses in physiopathology?

Giselle Charron, Evelyne Doudnikoff, Marie-Helene Canron, Qin Li, Céline Véga, Sebastien Marais, Jérôme Baufreton, Anne Vital, Stéphane H R Oliet, Erwan Bezard

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.1field-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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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  16. A Cell Atlas for the Mouse Brain.Frontiers in neuroinformatics · 2018
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  18. Molecular pharmacology · 2017
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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

10 authors at 5 institutions in 2 countries.

Giselle CharronInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France.
Evelyne DoudnikoffInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France.
Marie-Helene CanronInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France.
Qin LiInstitute of Laboratory Animal Sciences, Chinese Academy of Medical Science and Peking Union Medical College Beijing, China.
Céline VégaCNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France ; UFR Sciences de la Vie, University Pierre et Marie Curie (UPMC) Paris, France.
Sebastien MaraisBordeaux Imaging Center, UMS 3420, Université de Bordeaux Bordeaux, France ; CNRS, Bordeaux Imaging Center, UMS 3420 Bordeaux, France ; INSERM, Bordeaux Imaging Center, US 004 Bordeaux, France.
Jérôme BaufretonInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France.
Anne VitalInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France.
Stéphane H R OlietNeurocentre Magendie, U862, Institut National de la Santé et de la Recherche Médicale Bordeaux, France.
Erwan BezardInstitut des Maladies Neurodégénératives, Université de Bordeaux, UMR 5293 Bordeaux, France ; CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux, France ; Institute of Laboratory Animal Sciences, Chinese Academy of Medical Science and Peking Union Medical College Beijing, China.
Institut des Maladies Neurodégénératives · FRCentre National de la Recherche Scientifique · FRChinese Academy of Medical Sciences & Peking Union Medical College · CNNeurocentre Magendie · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current concept of basal ganglia organization and function in physiological and pathophysiological conditions excludes the most numerous cells in the brain, i.e., the astrocytes, present with a ratio of 10:1 neuron. Their role in neurodegenerative condition such as Parkinson's disease (PD) remains to be elucidated. Before embarking into physiological investigations of the yet-to-be-identified "tripartite" synapses in the basal ganglia in general and the striatum in particular, we therefore characterized anatomically the PD-related modifications in astrocytic morphology, the changes in astrocytic network connections and the consequences on the spatial relationship between astrocytic processes and asymmetric synapses in normal and PD-like conditions in experimental and human PD. Our results unravel a dramatic regulation of striatal astrocytosis supporting the hypothesis of a key role in (dys) regulating corticostriatal transmission. Astrocytes and their various properties might thus represent a therapeutic target in PD.

Indexed as

astrocytedopaminehumanimmunohistochemistrymedium spiny neuronmonkeymouserat

Identifiers

PMID25309435
PMCPMC4174038
OpenAlexW1971454855

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.