Evidence map›Paper›PMID 40042199›Full record

ArticleThe European journal of neuroscience2025

Neurophysiological Treatment Effects of Mesdopetam, Pimavanserin and Amantadine in a Rodent Model of Levodopa-Induced Dyskinesia.

Abdolaziz Ronaghi, Tiberiu Loredan Stan, Sebastian A Barrientos, Pär Halje, Azat Nasretdinov, Luciano Censoni, Sebastian Sulis Sato, Evgenya Malinina, Joakim Tedroff, Nicholas Waters and 1 more

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Abdolaziz RonaghiDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.
Tiberiu Loredan StanThe Group for Integrative Neurophysiology and Neurotechnology, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Sebastian A BarrientosThe Group for Integrative Neurophysiology and Neurotechnology, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Pär HaljeThe Group for Integrative Neurophysiology and Neurotechnology, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Azat NasretdinovDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.
Luciano CensoniDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.ORCID 0000-0002-2786-7910
Sebastian Sulis SatoDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.
Evgenya MalininaDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.
Joakim TedroffIntegrative Research Laboratories Sweden AB, Göteborg, Sweden.
Nicholas WatersIntegrative Research Laboratories Sweden AB, Göteborg, Sweden.
Per PeterssonDepartment of Medical Translational Biology, Umeå University, Umeå, Sweden.ORCID 0000-0001-6697-0171

Funding

Åhlén FoundationInsamlingsstiftelsernaKonung Gustaf V:s och Drottning Victorias FoundationLU InnovationPromobiliaRoyal Physiographical Society in LundSwedish Parkinson FoundationThe Kempe FoundationThe Swedish Brain FoundationUmeå UniversityVetenskapsrådet 2018-02717Vetenskapsrådet 2020-00123Vetenskapsrådet 2021-01769Vinnova 2019-01458
6 · The paper itself

Abstract

Levodopa provides effective symptomatic treatment for Parkinson's disease. However, nonmotor symptoms are often insufficiently relieved, and its long-term use is complicated by motor fluctuations and dyskinesia. To clarify mechanisms of levodopa-induced dyskinesia and pharmacological interventions aimed at reducing dyskinetic symptoms, we have here characterized the neurophysiological activity patterns in sensorimotor and cognitive-limbic circuits in dyskinetic rats, comparing the effects of amantadine, pimavanserin, and the novel prospective antidyskinetic and antipsychotic treatment mesdopetam. Parallel recordings of local field potentials from 11 cortical and subcortical regions revealed suppression of narrowband gamma oscillations (NBGs) in sensorimotor structures by amantadine and mesdopetam in conjunction with alleviation of dyskinetic signs. Concomitant gamma oscillations in cognitive-limbic circuits were not directly linked to dyskinesia and were not affected by antidyskinetic treatments to the same extent, although treatment-induced reductions in functional coupling were observed in both sensorimotor and cognitive-limbic circuits, in parallel. In a broad frequency spectrum (1-200 Hz), mesdopetam treatment displayed greater similarities to pimavanserin than to amantadine. These findings point to the reduction of NBGs as a valuable biomarker for the characterization of antidyskinetic treatment effects and provide systems-level mechanistic insights into the antidyskinetic efficacy of mesdopetam, with potential additional benefits for the treatment of Parkinson's-related psychosis.

Indexed as

AmantadineAntiparkinson AgentsDyskinesia, Drug-InducedLevodopaPiperidinesUreaAnimalsDisease Models, AnimalGamma RhythmMalePhenyl EthersPropylaminesRatsRats, Sprague-DawleyAmantadineAntiparkinson AgentsLevodopamesdopetamPhenyl EtherspimavanserinPiperidinesPropylaminesUreaLFPmulti‐electrodeoscillations

Identifiers

PMID40042199
PMCPMC11881547

What OpenQuestion holds

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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.