Evidence map›Paper›PMID 32680996›Full record

ArticleCommunications biology2020

The cardiolipin-binding peptide elamipretide mitigates fragmentation of cristae networks following cardiac ischemia reperfusion in rats.

Mitchell E Allen, Edward Ross Pennington, Justin B Perry, Sahil Dadoo, Marina Makrecka-Kuka, Maija Dambrova, Fatiha Moukdar, Hetal D Patel, Xianlin Han, Grahame K Kidd and 5 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 85 citations in OpenAlex.

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  18. Contemporary insights into elamipretide's mitochondrial mechanism of action and therapeutic effects.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2025
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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

15 authors at 7 institutions in 2 countries.

Mitchell E Allen *Department of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA.
Edward Ross Pennington *Department of Biochemistry and Molecular Biology, East Carolina University, Greenville, NC, USA.
Justin B PerryDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA.
Sahil DadooDepartment of Nutrition, Gillings School of Global Public Health and School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Marina Makrecka-KukaLatvian Institute for Organic Synthesis Riga Latvia, Norwich, UK.ORCID http://orcid.org/0000-0003-4549-1993
Maija DambrovaLatvian Institute for Organic Synthesis Riga Latvia, Norwich, UK.ORCID http://orcid.org/0000-0002-1739-0928
Fatiha MoukdarDepartment of Physiology, East Carolina University, Greenville, NC, USA.
Hetal D PatelDepartment of Physiology, East Carolina University, Greenville, NC, USA.
Xianlin HanBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA.ORCID http://orcid.org/0000-0002-8615-2413
Grahame K KiddDepartment of Neurosciences, Cleveland Clinic, Cleveland, OH, USA.
Emily K BensonRenovo Neural Inc, Cleveland, OH, USA.
Tristan B RaischVirginia Tech Faculty of Health Sciences, Roanoke, VA, USA.
Steven PoelzingVirginia Tech Faculty of Health Sciences, Roanoke, VA, USA.ORCID http://orcid.org/0000-0002-6979-1264
David A BrownDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, VA, USA.
Saame Raza ShaikhDepartment of Nutrition, Gillings School of Global Public Health and School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. shaikhsa@email.unc.edu.ORCID http://orcid.org/0000-0003-1950-2521
University of North Carolina at Chapel Hill · USVirginia Tech · USCarilion Roanoke Memorial Hospital · USEast Carolina University · USLatvijas Organiskās Sintēzes Institūts · LVCleveland Clinic · USThe University of Texas Health Science Center at San Antonio · US

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
Role of the Extracellular Space as a Modulator of the Cardiac Gap Junction - Conduction Velocity RelationshipR01HL102298 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI POELZING, STEVEN · 2011 to 2020
$3.9M
Signaling in Inherited and Acquired Sodium Channel Gain of FunctionR01HL138003 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI POELZING, STEVEN, WEINBERG, SETH HOWARD · 2018 to 2021
$2.6M
The Role of the Sodium Channel Beta Subunit in Cardiac ConductionR01HL141855 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI GOURDIE, ROBERT G, POELZING, STEVEN · 2018 to 2021
$1.8M
Mitochondrial respirasomes in acute coronary syndromesR01HL123647 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HULVER, MATTHEW W, SHAIKH, SAAME R · 2015 to 2018
$1.4M
NHLBI NIH HHS 1R01HL12364NHLBI NIH HHS R01 HL102298NHLBI NIH HHS R01 HL123647NHLBI NIH HHS R01 HL138003NHLBI NIH HHS R01 HL141855NIA NIH HHS P30 AG013319NIH HHS P30DK056350
6 · The paper itself

Abstract

Mitochondrial dysfunction contributes to cardiac pathologies. Barriers to new therapies include an incomplete understanding of underlying molecular culprits and a lack of effective mitochondria-targeted medicines. Here, we test the hypothesis that the cardiolipin-binding peptide elamipretide, a clinical-stage compound under investigation for diseases of mitochondrial dysfunction, mitigates impairments in mitochondrial structure-function observed after rat cardiac ischemia-reperfusion. Respirometry with permeabilized ventricular fibers indicates that ischemia-reperfusion induced decrements in the activity of complexes I, II, and IV are alleviated with elamipretide. Serial block face scanning electron microscopy used to create 3D reconstructions of cristae ultrastructure reveals that disease-induced fragmentation of cristae networks are improved with elamipretide. Mass spectrometry shows elamipretide did not protect against the reduction of cardiolipin concentration after ischemia-reperfusion. Finally, elamipretide improves biophysical properties of biomimetic membranes by aggregating cardiolipin. The data suggest mitochondrial structure-function are interdependent and demonstrate elamipretide targets mitochondrial membranes to sustain cristae networks and improve bioenergetic function.

Indexed as

AnimalsCardiolipinsCardiotonic AgentsHydrogen PeroxideMaleMass SpectrometryMicroscopy, Electron, TransmissionMitochondria, HeartMitochondrial MembranesMyocardial Reperfusion InjuryOligopeptidesRatsRats, Sprague-Dawleyarginyl-2,'6'-dimethyltyrosyl-lysyl-phenylalaninamideCardiolipinsCardiotonic AgentsHydrogen PeroxideOligopeptides

Identifiers

PMID32680996
PMCPMC7368046
OpenAlexW3042825564

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.