Evidence map›Paper›PMID 31968546›Full record

ArticleCells2020

PPARγ-Independent Side Effects of Thiazolidinediones on Mitochondrial Redox State in Rat Isolated Hearts.

Matthias L Riess, Reem Elorbany, Dorothee Weihrauch, David F Stowe, Amadou K S Camara

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Effects of Brown Rice, Meal Replacements, and Anti-Obesity Drugs on Mitochondria in Obese Rats.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  7. Review
  8. Remarks on Mitochondrial Myopathies.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
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.

Matthias L RiessAnesthesiology, TVHS VA Medical Center, Nashville, TN 37212, USA.ORCID 0000-0001-8748-5757
Reem ElorbanyInterdisciplinary Scientist Training Program, University of Chicago, Chicago, IL 60637, USA.ORCID 0000-0002-2059-6767
Dorothee WeihrauchDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
David F StoweDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Amadou K S CamaraDepartment of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.ORCID 0000-0002-7652-1414
Medical College of Wisconsin · USUniversity of Chicago · USVanderbilt University · US

Funding

Reperfusion Injury Protection Strategies During Basic Life SupportR01HL123227 · NHLBI · UNIVERSITY OF MINNESOTA · PI YANNOPOULOS, DEMETRIS · 2013 to 2017
$5.1M
Novel Copolymer-based Cell Membrane Stabilizers to Attenuate Myocardial InfarctionI01BX003482 · VA · VETERANS HEALTH ADMINISTRATION · PI RIESS, MATTHIAS L. · 2018 to 2022
–
Genetic Mechanisms of Resistance against Cardiac PreconditioningIK2BX001278 · VA · CLEMENT J. ZABLOCKI VA MEDICAL CENTER · PI RIESS, MATTHIAS L. · 2011 to 2014
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BLRD VA I01 BX003482BLRD VA IK2 BX001278NHLBI NIH HHS R01 HL123227
6 · The paper itself

Abstract

The effect of anti-diabetic thiazolidinediones (TZDs) on contributing to heart failure and cardiac ischemia/reperfusion (IR) injury is controversial. In this study we investigated the effect of select TZDs on myocardial and mitochondrial function in Brown Norway rat isolated hearts. In a first set of experiments, the TZD rosiglitazone was given acutely before global myocardial IR, and pre- and post-IR function and infarct size were assessed. In a second set of experiments, different concentrations of rosiglitazone and pioglitazone were administered in the presence or absence of the specific PPARγ antagonist GW9662, and their effects on the mitochondrial redox state were measured by online NADH and FAD autofluorescence. The administration of rosiglitazone did not significantly affect myocardial function except for transiently increasing coronary flow, but it increased IR injury compared to the control hearts. Both TZDs resulted in dose-dependent, reversible increases in mitochondrial oxidation which was not attenuated by GW9662. Taken together, these data suggest that TZDs cause excessive mitochondrial uncoupling by a PPARγ-independent mechanism. Acute rosiglitazone administration before IR was associated with enhanced cardiac injury. If translated clinically, susceptible patients on PPARγ agonists may experience enhanced myocardial IR injury by mitochondrial dysfunction.

Indexed as

AnimalsFlavin-Adenine DinucleotideFluorescenceMaleMitochondria, HeartMyocardial Reperfusion InjuryNADOxidation-ReductionPPAR gammaRats, Inbred BNThiazolidinedionesFlavin-Adenine DinucleotideNADPPAR gammaThiazolidinedionesGW9662ischemia reperfusion injuryLangendorffmyocardialpioglitazoneredox staterosiglitazoneTZDuncoupling

Identifiers

PMID31968546
PMCPMC7017211
OpenAlexW2998744759

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.