Evidence map›Paper›PMID 26843639›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Imaging Dopamine and Serotonin Systems on MPTP Monkeys: A Longitudinal PET Investigation of Compensatory Mechanisms.

Benedicte Ballanger, Maude Beaudoin-Gobert, Sara Neumane, Justine Epinat, Elise Metereau, Sandra Duperrier, Emmanuel Broussolle, Stephane Thobois, Frederic Bonnefoi, Christian Tourvielle and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Dysfunction of motor cortices in Parkinson's disease.Cerebral cortex (New York, N.Y. : 1991) · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Nonhuman Primates in Translational Research.Annual review of animal biosciences · 2022
    Review
  10. Article
  11. Basal ganglia beta oscillations during sleep underlie Parkinsonian insomnia.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Serotonergic targets for the treatment of L-DOPA-induced dyskinesia.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  16. Review
  17. Non-human primate models of PD to test novel therapies.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  18. Review
  19. Article
  20. 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

16 authors at 2 institutions in 1 country.

Benedicte BallangerCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
Maude Beaudoin-GobertCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.ORCID http://orcid.org/0000-0002-3056-2384
Sara NeumaneCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
Justine EpinatCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
Elise MetereauCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.ORCID http://orcid.org/0000-0001-6868-315X
Sandra DuperrierCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
Emmanuel BroussolleCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France, Hospices Civils de Lyon, Lyon 69229, France.
Stephane ThoboisCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France, Hospices Civils de Lyon, Lyon 69229, France.
Frederic BonnefoiCentre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France.
Christian TourvielleCentre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France.
Franck LavenneCentre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France.
Nicolas CostesCentre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France.
Didier LebarsUniversité Claude Bernard Lyon 1, Villeurbanne 69100, France, Centre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France, Institut de Chimie et de Biochimie Moléculaires et Supramoléculaires, Unité Mixte de Recherche 5246 Centre National de la Recherche Scientifique, Lyon 69622, France, and Hospices Civils de Lyon, Lyon 69229, France.
Luc ZimmerUniversité Claude Bernard Lyon 1, Villeurbanne 69100, France, Centre d'Exploration et de Recherche Médicale par Emission de Positons, Imagerie du vivant, Bron 69677, France, Hospices Civils de Lyon, Lyon 69229, France.
Véronique Sgambato-FaureCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.ORCID http://orcid.org/0000-0002-8792-8586
Léon TremblayCentre de Neurosciences Cognitives, Unité Mixte de Recherche 5229 Centre National de la Recherche Scientifique, Bron 69675, France, Université Claude Bernard Lyon 1, Villeurbanne 69100, France, leon.tremblay@isc.cnrs.fr.ORCID http://orcid.org/0000-0001-8370-6903
Université Claude Bernard Lyon 1 · FRCentre d'Exploration et de Recherche Médicale par Emission de Positons · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is now widely accepted that compensatory mechanisms are involved during the early phase of Parkinson's disease (PD) to delay the expression of motor symptoms. However, the neurochemical mechanisms underlying this presymptomatic period are still unclear. Here, we measured in vivo longitudinal changes of both the dopaminergic and serotonergic systems in seven asymptomatic 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-intoxicated monkeys (when motor symptoms are less apparent) using PET. We used the progressively MPTP-intoxicated monkey model that expresses recovery from motor symptoms to study the changes in dopamine synthesis ([(18)F]DOPA), dopamine D2/D3 receptors ([(11)C]raclopride), and serotonin transporter (11)C-N,N-dimethyl-2-(-2-amino-4-cyanophenylthio) benzylamine ([(11)C]DASB) and serotonin 1A receptor ([(18)F]MPPF) levels between four different states (baseline, early symptomatic, full symptomatic and recovered). During the early symptomatic state, we observed increases of [(18)F]DOPA uptake in the anterior putamen, [(11)C]raclopride binding in the posterior striatum, and 2'-methoxyphenyl-(N-2'-pyridinyl)-p-[(18)F]fluoro-benzamidoethylpiperazine [(18)F]MPPF uptake in the orbitofrontal cortex and dorsal ACC. After recovery from motor symptoms, the results mainly showed decreased [(11)C]raclopride binding in the anterior striatum and limbic ACC. In addition, our findings supported the importance of pallidal dopaminergic neurotransmission in both the early compensatory mechanisms and the functional recovery mechanisms, with reduced aromatic L-amino acid decarboxylase (AAAD) activity closely related to the appearance or perseveration of motor symptoms. In parallel, this study provides preliminary evidence of the role of the serotonergic system in compensatory mechanisms. Nonetheless, future studies are needed to determine whether there are changes in SERT availability in the early symptomatic state and if [(18)F]MPPF PET imaging might be a promising biomarker of early degenerative changes in PD. SIGNIFICANCE STATEMENT: The present research provides evidence of the potential of combining a multitracer PET imaging technique and a longitudinal protocol applied on a progressively 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated monkey model to further elucidate the nature of the compensatory mechanisms involved in the preclinical period of Parkinson's disease (PD). In particular, by investigating the dopaminergic and serotonergic changes both presynaptically and postsynaptically at four different motor states (baseline, early symptomatic, full symptomatic, and recovered), this study has allowed us to identify putative biomarkers for future therapeutic interventions to prevent and/or delay disease expression. For example, our findings suggest that the external pallidum could be a new target for cell-based therapies to reduce PD symptoms.

Indexed as

AnimalsCorpus StriatumDopaminergic NeuronsLongitudinal StudiesMacaca fascicularisMaleParkinsonian DisordersPositron-Emission TomographySerotonergic Neuronscompensatory mechanismsdopamineMPTPParkinson's diseasePET imagingserotonin

Identifiers

PMID26843639
PMCPMC6601989
OpenAlexW2265528762

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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.