Evidence map›Paper›PMID 38887858›Full record

ArticleCNS neuroscience & therapeutics2024

The selective butyrylcholinesterase inhibitor UW-MD-95 shows symptomatic and neuroprotective effects in a pharmacological mouse model of Alzheimer's disease.

Allison Carles, Matthias Hoffmann, Matthias Scheiner, Lucie Crouzier, Christelle Bertrand-Gaday, Arnaud Chatonnet, Michael Decker, Tangui Maurice

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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

8 authors.

Allison CarlesMMDN, Univ Montpellier, INSERM, EPHE, Montpellier, France.ORCID 0000-0002-4639-2244
Matthias HoffmannPharmazeutische und Medizinische Chemie, Institut für Pharmazie und Lebensmittelchemie, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.
Matthias ScheinerPharmazeutische und Medizinische Chemie, Institut für Pharmazie und Lebensmittelchemie, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.ORCID 0000-0003-0596-4725
Lucie CrouzierMMDN, Univ Montpellier, INSERM, EPHE, Montpellier, France.ORCID 0000-0001-8534-8337
Christelle Bertrand-GadayDMEM, Univ Montpellier, INRAE, Montpellier, France.ORCID 0000-0003-0461-2402
Arnaud ChatonnetDMEM, Univ Montpellier, INRAE, Montpellier, France.ORCID 0000-0002-4057-3896
Michael DeckerPharmazeutische und Medizinische Chemie, Institut für Pharmazie und Lebensmittelchemie, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.ORCID 0000-0002-6773-6245
Tangui MauriceMMDN, Univ Montpellier, INSERM, EPHE, Montpellier, France.ORCID 0000-0002-4074-6793

Funding

Agence Nationale de la Recherche 22-CE92-0080Deutsche Forschungsgemeinschaft DE 1536/12-1Deutscher Akademischer Austauschdienst 57702280Franco-Bavarian University Cooperation Center FK03-2020Programme Hubert Curien Procope (Campus France)
6 · The paper itself

Abstract

aimsAlzheimer's disease (AD) is a devastating dementia characterized by extracellular amyloid-β (Aβ) protein aggregates and intracellular tau protein deposition. Clinically available drugs mainly target acetylcholinesterase (AChE) and indirectly sustain cholinergic neuronal tonus. Butyrylcholinesterase (BChE) also controls acetylcholine (ACh) turnover and is involved in the formation of Aß aggregates and senile plaques. UW-MD-95 is a novel carbamate-based compound acting as a potent pseudo-irreversible BChE inhibitor, with high selectivity versus AChE, and showing promising protective potentials in AD.

methodsWe characterized the neuroprotective activity of UW-MD-95 in mice treated intracerebroventricularly with oligomerized Aβ

resultsWhen injected acutely 30 min before the behavioral tests (spontaneous alternation in the Y-maze, object recognition, or passive avoidance), UW-MD-95 (0.3-3 mg/kg) showed anti-amnesic effects in Aβ

conclusionUW-MD-95 appeared as a potent neuroprotective compound in the Aβ

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesButyrylcholinesteraseCholinesterase InhibitorsNeuroprotective AgentsPeptide FragmentsAnimalsDisease Models, AnimalDose-Response Relationship, DrugMaleMaze LearningMiceMice, Inbred C57BLOxidative StressAmyloid beta-Peptidesamyloid beta-protein (25-35)ButyrylcholinesteraseCholinesterase InhibitorsNeuroprotective AgentsPeptide FragmentsAlzheimer's diseaseAβ25‐35Butyrylcholinesteraseirreversible inhibitionneuroprotectionsymptomatic effectUW‐MD‐95

Identifiers

PMID38887858
PMCPMC11183908

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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.