Evidence map›Paper›PMID 39774033›Full record

ArticleNPJ Parkinson's disease2025

Brainstem serotonin amplifies nociceptive transmission in a mouse model of Parkinson's disease.

Zoé Grivet, Franck Aby, Aude Verboven, Rabia Bouali-Benazzouz, Benjamin Sueur, François Maingret, Frédéric Naudet, Thibault Dhellemmes, Philippe De Deurwaerdere, Abdelhamid Benazzouz and 1 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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.

Zoé GrivetUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Franck AbyUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Aude VerbovenUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Rabia Bouali-BenazzouzUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Benjamin SueurUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
François MaingretUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Frédéric NaudetUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Thibault DhellemmesUniversité de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.
Philippe De DeurwaerdereUniversité de Bordeaux, Institut des neurosciences cognitives et intégratives d'aquitaine, Bordeaux, France.
Abdelhamid Benazzouz *Université de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.ORCID http://orcid.org/0000-0002-2282-1120
Pascal Fossat *Université de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France. pascal.fossat@u-bordeaux.fr.ORCID http://orcid.org/0000-0001-5117-0817

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-19-CE16-0016Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE17-0003-01Association France Parkinson (France Parkinson) 2022-049
6 · The paper itself

Abstract

Parkinson's disease arises from the degeneration of dopaminergic neurons in the substantia nigra pars compacta, leading to motor symptoms such as akinesia, rigidity, and tremor at rest. The non-motor component of Parkinson's disease includes increased neuropathic pain, the prevalence of which is 4 to 5 times higher than the general rate. By studying a mouse model of Parkinson's disease induced by 6-hydroxydopamine, we assessed the impact of dopamine depletion on pain modulation. Mice exhibited mechanical hypersensitivity associated with hyperexcitability of neurons in the dorsal horn of the spinal cord (DHSC). Serotonin (5-HT) levels increased in the spinal cord, correlating with reduced tyrosine hydroxylase (TH) immunoreactivity in the nucleus raphe magnus (NRM) and increased excitability of 5-HT neurons. Selective optogenetic inhibition of 5-HT neurons attenuated mechanical hypersensitivity and reduced DHSC hyperexcitability. In addition, the blockade of 5-HT

Identifiers

PMID39774033
PMCPMC11706991

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Registered trials

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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.