Evidence map›Paper›PMID 29535397›Full record

ArticleScientific reports2018

Drosophila Ubiquitin C-Terminal Hydrolase Knockdown Model of Parkinson's Disease.

Hiep H Tran, Suong N A Dang, Thanh T Nguyen, Anh M Huynh, Linh M Dao, Kaeko Kamei, Masamitsu Yamaguchi, Thao T P Dang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  17. Dietary Antioxidants and Parkinson's Disease.Antioxidants (Basel, Switzerland) · 2020
    Review
  18. Review
  19. Evaluating the Potential ofParkinson's disease · 2019
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  20. 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

8 authors at 2 institutions in 2 countries.

Hiep H TranDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam.ORCID 0000-0001-5312-8989
Suong N A DangDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam.
Thanh T NguyenDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam.
Anh M HuynhDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam.
Linh M DaoDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam.
Kaeko KameiDepartment of Biomolecular Engineering, Kyoto Institute of Technology, Kyoto, 606-8585, Japan.
Masamitsu YamaguchiDepartment of Applied Biology, Kyoto Institute of Technology, Kyoto, 606-8585, Japan.
Thao T P DangDepartment of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University - Ho Chi Minh City, Ho Chi Minh City, 70000, Vietnam. dtpthao@hcmus.edu.vn.
Vietnam National University Ho Chi Minh City · VNKyoto Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder worldwide. Many factors have been shown to contribute to its pathogenesis including genetic and environmental factors. Ubiquitin C-terminal hydrolase L1 (UCHL1) is also known to be involved in the pathogenesis of PD. We herein modeled the study of UCHL1 in Drosophila melanogaster and investigated its functions in PD. The specific knockdown of the Drosophila ortholog of UCHL1 (dUCH) in dopaminergic neurons (DA neurons) led to the underdevelopment and/or degeneration of these neurons, specifically in DL1 DA neuron cluster in the larval brain lobe and PPM2, PPM3, PPL2ab, and VUM DA neuron clusters in the adult brain. These defects were followed by a shortage of dopamine in the brain, which subsequently resulted in locomotor dysfunction. The degeneration of DA neurons in dUCH knockdown adult brain, which occurred progressively and severely during the course of aging, mimics the epidemiology of PD. DA neuron and locomotor defects were rescued when dUCH knockdown flies were treated with vitamin C, a well-known antioxidant. These results suggest that dUCH knockdown fly is a promising model for studying the pathogenesis and epidemiology of PD as well as the screening of potential antioxidants for PD therapeutics.

Indexed as

Disease Models, AnimalAnimalsAntioxidantsAscorbic AcidDopamineDopaminergic NeuronsDrosophila melanogasterDrosophila ProteinsGene Knockdown TechniquesHumansMaleOxidative StressParkinson DiseaseUbiquitin ThiolesteraseAntioxidantsAscorbic AcidDopamineDrosophila ProteinsUbiquitin ThiolesteraseUCH protein, Drosophila

Identifiers

PMID29535397
PMCPMC5849740
OpenAlexW2790393414

What OpenQuestion holds

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LicenceCC BY
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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.