Evidence map›Paper›PMID 24568130›Full record

ArticleRadiation research2014

Radiation-induced alterations in mitochondria of the rat heart.

Vijayalakshmi Sridharan, Nukhet Aykin-Burns, Preeti Tripathi, Kimberly J Krager, Sunil K Sharma, Eduardo G Moros, Peter M Corry, Grazyna Nowak, Martin Hauer-Jensen, Marjan Boerma

Abstract read
In one paragraph

Article in Radiation research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Chemo-/radiotherapy-induced cardiomyopathy: roles of mitochondria and endoplasmic reticulum.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. [Radiation-Induced Heart Disease: Current Status and Challenges].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2022
    Review
  15. Cardiac fibrosis in oncologic therapies.Current opinion in physiology · 2022
    Article
  16. Mitochondrial CaArteriosclerosis, thrombosis, and vascular biology · 2022
    Article
  17. Article
  18. Review
  19. Review
  20. Characterization of cardiovascular injury in mice following partial-heart irradiation with clinically relevant dose and fractionation.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2021
    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

10 authors at 3 institutions in 1 country.

Vijayalakshmi Sridharana University of Arkansas for Medical Sciences, Department of Pharmaceutical Sciences, Division of Radiation Health, Little Rock, Arkansas.
Nukhet Aykin-Burns
Preeti Tripathi
Kimberly J Krager
Sunil K Sharma
Eduardo G Moros
Peter M Corry
Grazyna Nowak
Martin Hauer-Jensen
Marjan Boerma
University of Arkansas for Medical Sciences · USCentral Arkansas Veterans Healthcare System · USMoffitt Cancer Center · US

Funding

Molecular Pathogenesis of Radiation EnteropathyR37CA071382 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI HAUER-JENSEN, MARTIN · 2008 to 2013
$1.7M
MOLECULAR PATHOGENESIS OF RADIATION ENTEROPATHYR01CA071382 · NCI · UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK · PI HAUER-JENSEN, MARTIN · 1997 to 2005
$1.6M
Radiation-Induced Heart Disease: Mechanisms and InterventionsR01CA148679 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI BOERMA, MARJAN · 2010 to 2014
$1.4M
Sirt3: A Key Player Against PCB-Induced Mitochondrial InjuryR15ES022781 · NIEHS · UNIV OF ARKANSAS FOR MED SCIS · PI AYKIN-BURNS, NUKHET · 2013 to 2013
$443k
NCI NIH HHS CA148679NCI NIH HHS CA71382NCI NIH HHS R01 CA071382NCI NIH HHS R01 CA148679NCI NIH HHS R37 CA071382NIEHS NIH HHS R15 ES022781
6 · The paper itself

Abstract

Radiation therapy for the treatment of thoracic cancers may be associated with radiation-induced heart disease (RIHD), especially in long-term cancer survivors. Mechanisms by which radiation causes heart disease are largely unknown. To identify potential long-term contributions of mitochondria in the development of radiation-induced heart disease, we examined the time course of effects of irradiation on cardiac mitochondria. In this study, Sprague-Dawley male rats received image-guided local X irradiation of the heart with a single dose ranging from 3-21 Gy. Two weeks after irradiation, left ventricular mitochondria were isolated to assess the dose-dependency of the mitochondrial permeability transition pore (mPTP) opening in a mitochondrial swelling assay. At time points from 6 h to 9 months after a cardiac dose of 21 Gy, the following analyses were performed: left ventricular Bax and Bcl-2 protein levels; apoptosis; mitochondrial inner membrane potential and mPTP opening; mitochondrial mass and expression of mitophagy mediators Parkin and PTEN induced putative kinase-1 (PINK-1); mitochondrial respiration and protein levels of succinate dehydrogenase A (SDHA); and the 70 kDa subunit of complex II. Local heart irradiation caused a prolonged increase in Bax/Bcl-2 ratio and induced apoptosis between 6 h and 2 weeks. The mitochondrial membrane potential was reduced until 2 weeks, and the calcium-induced mPTP opening was increased from 6 h up to 9 months. An increased mitochondrial mass together with unaltered levels of Parkin suggested that mitophagy did not occur. Lastly, we detected a significant decrease in succinate-driven state 2 respiration in isolated mitochondria from 2 weeks up to 9 months after irradiation, coinciding with reduced mitochondrial levels of succinate dehydrogenase A. Our results suggest that local heart irradiation induces long-term changes in cardiac mitochondrial membrane functions, levels of SDH and state 2 respiration. At any time after exposure to radiation, cardiac mitochondria are more prone to mPTP opening. Future studies will determine whether this makes the heart more susceptible to secondary stressors such as calcium overload or ischemia/reperfusion.

Indexed as

AnimalsApoptosisbcl-2-Associated X ProteinCell RespirationMaleMembrane Potential, MitochondrialMitochondriaMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreMyocardiumProtein ConformationProto-Oncogene Proteins c-bcl-2RatsRats, Sprague-DawleyTime FactorsUp-Regulationbcl-2-Associated X ProteinMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreProto-Oncogene Proteins c-bcl-2

Identifiers

PMID24568130
PMCPMC4029615
OpenAlexW2037883815

What OpenQuestion holds

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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.