Evidence map›Paper›PMID 31625972›Full record

ArticleBehavioural pharmacology2020

Measurement of baseline locomotion and other behavioral traits in a common marmoset model of Parkinson's disease established by a single administration regimen of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine: providing reference data for efficacious preclinical evaluations.

Kiyoshi Ando, Takashi Inoue, Keigo Hikishima, Yuji Komaki, Kenji Kawai, Ryo Inoue, Chiyoko Nishime, Eiko Nishinaka, Koji Urano, Hideyuki Okano

Abstract read
In one paragraph

Article in Behavioural pharmacology, 2020. 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. Article
  2. Article
  3. Brain sciences · 2025
    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

10 authors.

Kiyoshi AndoCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Takashi InoueCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Keigo HikishimaCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Yuji KomakiCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Kenji KawaiCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Ryo InoueCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Chiyoko NishimeCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Eiko NishinakaCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Koji UranoCentral Institute for Experimental Animals (CIEA), Kawasakiku, Kawasaki.
Hideyuki OkanoKeio University, School of Medicine, Shinjukuku, Tokyo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Baseline locomotion and behavioral traits in the common marmoset Parkinson's disease model were examined to provide basic information for preclinical evaluations of medical treatments. A single regimen of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine at a cumulative dose of 5 mg/kg as the free base over three consecutive days was administered subcutaneously to 10 marmosets. Data obtained from these marmosets were compared to pre-1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine levels or 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine free marmosets. After the single regimen, reduced daily locomotion, a measure of immobility (a primary sign of Parkinsonism), was observed for more than a year. A moving tremor was also observed by visual inspection during this period. When apomorphine (0.13 mg/kg, s.c.) was administered, either right or left circling behavior was observed in a cylindrical chamber in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine marmosets, suggestive of unequal neural damage between the two brain hemispheres to different extents. MRI revealed that T1 relaxation time in the right substantia nigra correlated with right circling in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine marmosets. Histology was supportive of dopaminergic neural loss in the striatum. These results increase our understanding of the utility and limitations of the Parkinson's disease model in marmosets with a single 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine regimen, and provide reference data for efficacious preclinical evaluations.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAnimalsBehavior, AnimalBrainCallithrixCorpus StriatumDisease Models, AnimalDopamineLocomotionParkinson DiseaseParkinsonian DisordersSubstantia NigraTremor1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineDopamine

Identifiers

PMID31625972
PMCPMC6964884

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.