Evidence map›Paper›PMID 30933310›Full record

ArticleJournal of neurochemistry2019

Release parameters during progressive degeneration of dopamine neurons in a mouse model reveal earlier impairment of spontaneous than forced behaviors.

Yuan-Hao Chen, Tsung-Hsun Hsieh, Tung-Tai Kuo, Jen-Hsin Kao, Kuo-Hsing Ma, Eagle Yi-Kung Huang, Yu-Ching Chou, Lars Olson, Barry J Hoffer

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dopamine, behavior, and addiction.Journal of biomedical science · 2021
    Review
  6. Review
  7. Article
  8. Article
  9. Article
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

9 authors.

Yuan-Hao ChenDepartment of Neurological Surgery, Tri-Service General Hospital, Natl Defense Medical Center, Taipei, Taiwan, R.O.C.
Tsung-Hsun HsiehDepartment of Physical Therapy and Graduate Institute of Rehabilitation Science, Chang Gung University, Taoyuan, Taiwan.
Tung-Tai KuoGraduate Institute of Computer and Communication Engineering, Natl Taipei University of Technology, Taipei, Taiwan, R.O.C.
Jen-Hsin KaoDepartment of Neurological Surgery, Tri-Service General Hospital, Natl Defense Medical Center, Taipei, Taiwan, R.O.C.
Kuo-Hsing MaGraduate Institute of Biology and Anatomy, Natl Defense Medical Center, Tapipei, Taiwan, R.O.C.
Eagle Yi-Kung HuangDepartment of Pharmacology, Natl Defense Medical Center, Taipei, Taiwan, R.O.C.
Yu-Ching ChouSchool of Public Health, Natl Defense Medical Center, Taipei, Taiwan, R.O.C.
Lars OlsonDepartment of Neuroscience, Karolinska Institute, Stockholm, Sweden.
Barry J HofferGraduate Program on Neuroregeneration, Taipei Medical University, Taipei, Taiwan, R.O.C.ORCID 0000-0002-1122-9025

Funding

Repositioning Gliptins for Parkinson's Disease TreatmentR01NS094152 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI HOFFER, BARRY J, LUO, YU · 2015 to 2018
$1.1M
NINDS NIH HHS R01 NS094152StratNeuro
6 · The paper itself

Abstract

To determine the role of reduced dopaminergic transmission for declines of forced versus spontaneous behavior, we used a model of Parkinson's disease with progressive degeneration of dopamine (DA) neurons, the MitoPark mouse. Mice were subjected to rotarod tests of motor coordination, and open field and cylinder tests for spontaneous locomotor activity and postural axial support. To measure DA release in dorsal striatum and the shell of Nucleus Accumbens (NAc), we used ex vivo fast-scan cyclic voltammetry in 6- to 24-week-old mice. To determine decline of DA transporter function, we used 18FE-PE2I positron emission tomography. We show here that fast-scan cyclic voltammetry is a sensitive tool to detect evoked DA release dysfunction in MitoPark mice and that electrically evoked DA release is affected earlier in nigrostriatal than mesolimbic DA systems. DA reuptake was also affected more slowly in NAc shell. Positron emission tomography data showed DA uptake to be barely above detection levels in 16- and 20-week-old MitoPark mice. Rotarod performance was not impaired until mice were 16 weeks old, when evoked DA release in striatum had decreased to ≈ 40% of wild-type levels. In contrast, impairment of open field locomotion and rearing began at 10 weeks, in parallel with the initial modest decline of evoked DA release. We conclude that forced behaviors, such as motivation not to fall, can be partially maintained even when DA release is severely compromised, whereas spontaneous behaviors are much more sensitive to impaired DA release, and that presumed secondary non-dopaminergic system alterations do not markedly counteract or aggravate effects of severe impairment of DA release. OPEN SCIENCE BADGES: This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.

Indexed as

AnimalsBehavior, AnimalBrainDisease Models, AnimalDopamineDopaminergic NeuronsLocomotionMiceNerve DegenerationParkinsonian DisordersDopaminedopaminefast-scan cyclic voltammetryParkinson's diseasePETTFAM

Identifiers

PMID30933310
PMCPMC6592720

What OpenQuestion holds

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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.