Evidence map›Paper›PMID 24908200›Full record

ArticleInternational journal of cardiology2014

Intravenous (-)-epicatechin reduces myocardial ischemic injury by protecting mitochondrial function.

Katrina Go Yamazaki, Aleksander Y Andreyev, Pilar Ortiz-Vilchis, Susanna Petrosyan, Ajit S Divakaruni, Sandra E Wiley, Christine De La Fuente, Guy Perkins, Guillermo Ceballos, Francisco Villarreal and 1 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cardiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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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

11 authors at 3 institutions in 2 countries.

Katrina Go YamazakiCalifornia State University Los Angeles, Department of Biological Sciences, Los Angeles, CA, United States; University of California San Diego, United States. Electronic address: Katrina.Yamazaki@calstatela.edu.
Aleksander Y AndreyevDepartment of Pharmacology, La Jolla, CA, United States.
Pilar Ortiz-VilchisEscuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.
Susanna PetrosyanDepartment of Pharmacology, La Jolla, CA, United States.
Ajit S DivakaruniDepartment of Pharmacology, La Jolla, CA, United States.
Sandra E WileyDepartment of Pharmacology, La Jolla, CA, United States.
Christine De La FuenteCalifornia State University Los Angeles, Department of Biological Sciences, Los Angeles, CA, United States; University of California San Diego, United States.
Guy PerkinsNational Center for Microscopy and Imaging Research, La Jolla, CA, United States.
Guillermo CeballosDepartment of Medicine, La Jolla, CA, United States; Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico.
Francisco VillarrealDepartment of Medicine, La Jolla, CA, United States.
Anne N MurphyDepartment of Pharmacology, La Jolla, CA, United States.
La Jolla Alcohol Research · USCalifornia State University Los Angeles · USInstituto Politécnico Nacional · MX

Funding

Research Initiative for Scientific Enhancement (RISE)R25GM061331 · NIGMS · CALIFORNIA STATE UNIVERSITY LOS ANGELES · PI FOSTER, KRISHNA L · 2000 to 2021
$33.1M
Surgery, Physiology and ImmunohistopathologyP01HL085577 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2006 to 2017
$18.4M
IVEM and Image Analysis ResourceP41GM103412 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2012 to 2019
$17.9M
UNDERGRADUATE STUDENT TRAINING IN ACADEMIC RESEARCHT34GM008228 · NIGMS · CALIFORNIA STATE UNIVERSITY LOS ANGELES · PI TUNSTAD, LINDA M. · 1986 to 2022
$13.3M
San Diego EXPORT Comprehensive NCMHD Research CenterP60MD000220 · NIMHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO · 2002 to 2011
$11.0M
Molecular biology and mechanics of the cardiac interstitiumR01HL043617 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO J · 1989 to 2011
$3.5M
Effects of Cocoa Flavonols on Myocardial Infarction Size and Post-Injury InjuryR21AT004277 · NCCIH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO J · 2008 to 2009
$479k
Targeting cellular bioenergetics for the prevention and treatment of diabetesR24DK092154 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO J · 2011 to 2011
$459k
NCCIH NIH HHS AT4277NCCIH NIH HHS R21 AT004277NHLBI NIH HHS HL43617NHLBI NIH HHS P01 HL085577NHLBI NIH HHS R01 HL043617NIDDK NIH HHS DK92154NIDDK NIH HHS R24 DK092154NIGMS NIH HHS P41 GM103412NIGMS NIH HHS P41GM103412-24NIGMS NIH HHS R25 GM061331NIGMS NIH HHS T34 GM008228NIMHD NIH HHS MD000220NIMHD NIH HHS P60 MD000220
6 · The paper itself

Abstract

backgroundTargeting the mitochondria during ischemia/reperfusion (IR) can confer cardioprotection leading to improved clinical outcomes. The cardioprotective potential of (-)-epicatechin (EPI) during IR via modulation of mitochondrial function was evaluated. METHODS AND

resultsIschemia was induced in rats via a 45 min occlusion of the left anterior descending coronary artery followed by 1 h, 48 h, or 3 week reperfusion. EPI (10 mg/kg) was administered IV 15 min prior to reperfusion for the single dose group and again 12 h later for the double dose group. Controls received water. Experiments also utilized cultured neonatal rat ventricular myocytes (NRVM) and myoblasts. A single dose of EPI reduced infarct size by 27% at 48 h and 28% at 3 week. Double dose treatment further decreased infarct size by 80% at 48 h, and 52% by 3 weeks. The protective effect of EPI on mitochondrial function was evident after 1h of reperfusion when mitochondria demonstrated less respiratory inhibition, lower mitochondrial Ca2+ load, and a preserved pool of NADH that correlated with higher tissue ATP levels. Mechanistic studies in NRVM revealed that EPI acutely stimulated maximal rates of respiration, an effect that was blocked by inhibitors of the mitochondrial pyruvate carrier, nitric oxide synthase, or soluble guanylyl cyclase. In myoblasts, knockdown of components of the mitochondrial pyruvate carrier blocked EPI-induced respiratory stimulation.

conclusionsIV EPI confers cardioprotection via preservation of mitochondrial function potentially through enhanced substrate provision. These provocative results document a novel mechanism of a natural product with potential clinical utility.

Indexed as

AnimalsAnimals, NewbornCardiotonic AgentsCatechinCells, CulturedDose-Response Relationship, DrugInfusions, IntravenousMaleMitochondria, HeartMyocardial Reperfusion InjuryRatsRats, Sprague-DawleyCardiotonic AgentsCatechinCardiac metabolismEpicatechinMitochondrial Ca(2+)Mitochondrial pyruvate carrierMyocardial ischemia–reperfusion injury

Identifiers

PMID24908200
PMCPMC4506135
OpenAlexW2072196539

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.