Evidence map›Paper›PMID 20937256›Full record

ArticleBiochemical and biophysical research communications2010

Gene disruption of caspase-3 prevents MPTP-induced Parkinson's disease in mice.

Marina Yamada, Kotaro Kida, Willington Amutuhaire, Fumito Ichinose, Masao Kaneki

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 61 citations in OpenAlex.

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  19. Disrupted iron homeostasis causes dopaminergic neurodegeneration in mice.Proceedings of the National Academy of Sciences of the United States of America · 2016
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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

5 authors at 3 institutions in 1 country.

Marina YamadaDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA 02129, USA.
Kotaro Kida
Willington Amutuhaire
Fumito Ichinose
Masao Kaneki
Harvard University · USMassachusetts General Hospital · USShriners Hospitals for Children - Boston · US

Funding

Interdepartmental Neuroscience CenterP30NS045776 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI BREAKEFIELD, XANDRA OWENS, TANNOUS, BAKHOS A · 2003 to 2018
$11.1M
Inducible Nitric Oxide Synthase and Insulin ResistanceR01DK058127 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KANEKI, MASAO · 2002 to 2009
$2.1M
IMPACT OF HYDROGEN SULFIDE ON OUTCOME OF CARDIAC ARREST AND CARDIOPULMONARY RESUSR01HL101930 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ICHINOSE, FUMITO · 2010 to 2014
$2.1M
NHLBI NIH HHS R01 HL101930NIDDK NIH HHS R01 DK058127NIDDK NIH HHS R01 DK05827NINDS NIH HHS P30 NS045776
6 · The paper itself

Abstract

The development of Parkinson's disease is accompanied by concurrent activation of caspase-3 and apoptosis of dopaminergic neurons of human patients and rodent models. The role of caspase-3, a final executioner of apoptosis, in the pathogenesis of Parkinson's disease, however, remains to be determined. Here, we show that gene disruption of caspase-3 protects mice from 1-methyle-4-phenyl-1,2,3,6-tetrahmydropyridine (MPTP)-induced Parkinsonian syndrome, as reflected by reversal of MPTP-induced bradykinesia and decreased tyrosine hydroxylase expression in the nigra-striatum. MPTP treatment resulted in increased caspase-3 activation and apoptosis in the substantia nigra of wild-type mice at 24 h after the inception of MPTP treatment, as compared with vehicle-treated control animals. Gene disruption of caspase-3 prevented MPTP-induced apoptosis in the substantia nigra. At 7 days after MPTP treatment, tyrosine hydroxylase expression was suppressed and infiltration of activated microglia and astrocytes was markedly increased in the nigra-striatum of wild-type mice. All of these alterations following MPTP treatment were blocked by disruption of caspase-3 in mice. These results clearly indicate that caspase-3 activation is required for the development of MPTP-induced Parkinson's disease in mice. These findings suggest that activation of caspase-3-mediated apoptosis of dopaminergic neurons in the early stage may play an important role in the pathogenesis of Parkinson's disease.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAnimalsApoptosisCaspase 3Disease Models, AnimalEnzyme ActivationGene SilencingHypokinesiaMaleMiceMice, Inbred C57BLNeurotoxinsParkinson DiseaseParkinson Disease, SecondarySubstantia NigraTyrosine 3-Monooxygenase1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineCaspase 3NeurotoxinsTyrosine 3-Monooxygenase

Identifiers

PMID20937256
PMCPMC3292898
OpenAlexW1996239200

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.