Evidence map›Paper›PMID 27619562›Full record

ArticleScientific reports2016

Inhibition of Drp1 mitochondrial translocation provides neural protection in dopaminergic system in a Parkinson's disease model induced by MPTP.

Emily Filichia, Barry Hoffer, Xin Qi, Yu Luo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 154 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. SIRT3-Mediated Deacetylation of DRP1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  16. Review
  17. Review
  18. Metabolic Parkinson's disease.Frontiers in aging neuroscience · 2025
    Review
  19. The role of mitochondria in iron overload-induced damage.Journal of translational medicine · 2024
    Review
  20. Article

37 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Emily FilichiaDepartment of Neurological Surgery, Case Western Reserve University, Cleveland, USA.
Barry HofferDepartment of Neurological Surgery, Case Western Reserve University, Cleveland, USA.
Xin QiDepartment of Physiology &Biophysics, Case Western Reserve University, Cleveland, USA.
Yu LuoDepartment of Neurological Surgery, Case Western Reserve University, Cleveland, USA.
Case Western Reserve University · USNeurological Surgery · US

Funding

Genetic and drug modulation of sonic hedgehog pathway in brain ischemiaR01NS091213 · NINDS · UNIVERSITY OF CINCINNATI · PI LUO, YU · 2015 to 2019
$1.7M
Dynamin-related protein 1, neurodegeneration and Huntington's diseaseR01NS088192 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI QI, XIN · 2014 to 2018
$1.7M
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 NS088192NINDS NIH HHS R01 NS091213NINDS NIH HHS R01 NS094152
6 · The paper itself

Abstract

Accumulating evidence suggest mitochondria-mediated pathways play an important role in dopaminergic neuronal cell death in Parkinson's disease (PD). Drp1, a key regulator of mitochondrial fission, has been shown to be activated and translocated to mitochondria under stress, leading to excessive mitochondria fission and dopaminergic neuronal death in vitro. However, whether Drp1 inhibition can lead to long term stable preservation of dopaminergic neurons in PD-related mouse models remains unknown. In this study, using a classical MPTP animal PD model, we showed for the first time Drp1 activation and mitochondrial translocation in vivo after MPTP administration. Inhibition of Drp1 activation by a selective peptide inhibitor P110, blocked MPTP-induced Drp1 mitochondrial translocation and attenuated dopaminergic neuronal loss, dopaminergic nerve terminal damage and behavioral deficits caused by MPTP. MPTP-induced microglial activation and astrogliosis were not affected by P110 treatment. Instead, inhibition of Drp1 mitochondrial translocation diminished MPTP-induced p53, BAX and PUMA mitochondrial translocation. This study demonstrates that inhibition of Drp1 hyperactivation by a Drp1 peptide inhibitor P110 is neuroprotective in a MPTP animal model. Our data also suggest that the protective effects of P110 treatment might be mediated by inhibiting the p53 mediated apoptotic pathways in neurons through inhibition of Drp1-dependent p53 mitochondrial translocation.

Indexed as

AnimalsApoptosisDisease Models, AnimalDopamineDopaminergic NeuronsDynaminsGTP PhosphohydrolasesHumansMiceMitochondriaMitochondrial DynamicsMPTP PoisoningNeuroprotectionParkinson DiseaseParkinson Disease, SecondaryPeptide FragmentsDnm1l protein, mouseDopamineDynaminsGTP PhosphohydrolasesP110 peptidePeptide FragmentsTumor Suppressor Protein p53

Identifiers

PMID27619562
PMCPMC5020318
OpenAlexW2520855813

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.