Evidence map›Paper›PMID 31286348›Full record

ArticleMolecular imaging and biology2020

Longitudinal PET Imaging of α7 Nicotinic Acetylcholine Receptors with [

Steven Vetel, Johnny Vercouillie, Frédéric Buron, Jackie Vergote, Clovis Tauber, Julie Busson, Gabrielle Chicheri, Sylvain Routier, Sophie Sérrière, Sylvie Chalon

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In one paragraph

Article in Molecular imaging and biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Assessment of [Biomolecules · 2025
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  5. Development ofACS chemical neuroscience · 2022
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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 2 institutions in 1 country.

Steven VetelUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Johnny VercouillieUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Frédéric BuronInstitut de Chimie Organique et Analytique, ICOA, UMR CNRS 7311, Université d'Orléans, Orleans, France.
Jackie VergoteUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Clovis TauberUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Julie BussonUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Gabrielle ChicheriUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Sylvain RoutierInstitut de Chimie Organique et Analytique, ICOA, UMR CNRS 7311, Université d'Orléans, Orleans, France.
Sophie SérrièreUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France.
Sylvie ChalonUMR Inserm U1253, iBrain, Université de Tours, UFR de Médecine, 10 Boulevard Tonnellé, 37032, Tours Cedex 01, France. sylvie.chalon@univ-tours.fr.ORCID 0000-0003-1865-8380
Université de Tours · FRUniversité d'Orléans · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe nicotinic acetylcholine alpha-7 receptors (α7R) are involved in a number of neuropsychiatric and neurodegenerative brain disorders such as Parkinson's disease (PD). However, their specific pathophysiologic roles are still unclear. In this context, we studied the evolution of these receptors in vivo by positron emission tomography (PET) imaging using the recently developed tracer 3-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-6-[ PROCEDURES: PET imaging of α7R was performed at 3, 7, and 14 days following a partial striatal unilateral lesion with 6-hydroxydopamine in adult rats. After the last imaging experiments, the status of nigro-striatal dopamine neurons as well as different markers of neuroinflammation was evaluated on brain sections by autoradiographic and immunofluorescent experiments.

resultsWe showed an early and transitory rise in α7R expression in the lesioned striatum and substantia nigra, followed by over-expression of several gliosis activation markers in these regions of interest.

conclusionsThese findings support a longitudinally follow-up of α7R in animal models of PD and highlight the requirement to use a potential neuroprotective approach through α7R ligands at the early stages of PD.

Indexed as

Positron-Emission Tomographyalpha7 Nicotinic Acetylcholine ReceptorAmphetaminesAnimalsAutoradiographyAzabicyclo CompoundsBrainBrain MappingCyclic S-OxidesDisease Models, AnimalFluorine RadioisotopesMaleNeuroprotectionParkinson DiseaseRadiopharmaceuticalsRats3-(1,4-diazabicyclo(3.2.2)nonan-4-yl)-6-fluorodibenzo(b,d)thiophene 5,5-dioxidealpha7 Nicotinic Acetylcholine ReceptorAmphetaminesAzabicyclo CompoundsCyclic S-OxidesFluorine-18Fluorine RadioisotopesRadiopharmaceuticalsDopamine neurotransmissionM1/M2 phenotypeMicrogliaNeurodegenerationNeuroinflammation

Identifiers

PMID31286348
OpenAlexW2961548813

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.