Evidence map›Paper›PMID 28288978›Full record

ArticleJournal of the American Heart Association2017

Mff-Dependent Mitochondrial Fission Contributes to the Pathogenesis of Cardiac Microvasculature Ischemia/Reperfusion Injury via Induction of mROS-Mediated Cardiolipin Oxidation and HK2/VDAC1 Disassociation-Involved mPTP Opening.

Hao Zhou, Shunying Hu, Qinhua Jin, Chen Shi, Ying Zhang, Pingjun Zhu, Qiang Ma, Feng Tian, Yundai Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed
17.9field-weighted citation impact, top 1% 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

160 citing papers in PubMed, 303 citations in OpenAlex.

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100 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

9 authors at 2 institutions in 1 country.

Hao ZhouDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Shunying HuDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Qinhua JinDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Chen ShiDepartment of Radiation Oncology, Peking University Cancer Hospital and Institute, Beijing, China.
Ying ZhangDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Pingjun ZhuDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Qiang MaDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Feng TianDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Yundai ChenDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China yundaic@163.com cyundai@vip.163.com.
Chinese PLA General Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cardiac microvascular system ischemia/reperfusion injury following percutaneous coronary intervention is a clinical thorny problem. This study explores the mechanisms by which ischemia/reperfusion injury induces cardiac microcirculation collapse. METHODS AND

resultsIn wild-type mice, mitochondrial fission factor (Mff) expression increased in response to acute microvascular ischemia/reperfusion injury. Compared with wild-type mice, homozygous Mff-deficient (Mff

conclusionsThis evidence clearly illustrates that microcirculatory ischemia/reperfusion injury can be attributed to Mff-dependent mitochondrial fission via voltage-dependent anion channel 1/hexokinase 2-mediated mitochondrial permeability transition pore opening and mitochondrial reactive oxygen species/cardiolipin involved cyt-c release.

Indexed as

Gene Expression RegulationAnimalsApoptosisBlotting, WesternCardiolipinsCells, CulturedChromatography, High Pressure LiquidDisease Models, AnimalDNA, MitochondrialEndothelial CellsHexokinaseImmunohistochemistryMaleMembrane ProteinsMiceMicrocirculationCardiolipinsDNA, MitochondrialHexokinasehexokinase 2, mouseMembrane Proteinsmitochondrial fission factor, mouseMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMitochondrial ProteinsReactive Oxygen SpeciesVdac1 protein, mouseVoltage-Dependent Anion Channel 1apoptosisendothelial cellischemia/reperfusion injurymitochondria

Identifiers

PMID28288978
PMCPMC5524036
OpenAlexW2596407801

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.