The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Decreased complex III activity in mitochondria isolated from rat heart subjected to ischemia and reperfusion: role of reactive oxygen species and cardiolipin
Abstract
Reactive oxygen species (ROS) are considered an important factor in ischemia‐reperfusion injury to cardiac myocites. We have examined the effects of ischemia (30 min) and ischemia followed by reperfusion (15 min) of rat hearts on the activity of complex III and on the cardiolipin content in isolated mitochondria. Mitochondrial production of H 2 O 2 and lipid peroxidation was also measured. The capacity of mitochondria to produce both H 2 O 2 and lipid peroxidation increased upon reperfusion. The activity of complex III was 22% and 46% lower in ischemic and reperfused rat heart mitochondria, respectively, than that of controls. These changes in complex III activity were associated to parallel changes in state 3 respiration. The mitochondrial content of cardiolipin, which is required for optimal activity of complex III, decreased by 28% and by 50% as a function of ischemia and reperfusion, respectively. The lower complex III activity in mitochondria from reperfused rat hearts could be completely restored to the level of normal hearts by exogenously added cardiolipin. It is proposed that the loss of complex III activity in reperfused rat hearts can be mainly ascribed to a loss of cardiolipin content, due to oxidative attack by oxygen free radicals.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“peroxidation of mitochondrial phospholipids may affect the integrity of permeability transition pores (PTPs) and disaggregate complexes I and III of the respiratory chain, thereby enhancing electron leakage within the mitochondrial intermembrane space5,6.”
From ROS in cancer therapy: the bright side of the moon (2020) · cites this paper as [6]
Citations
Cites
A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION
Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/o59-099 · Cited by 54,751
[30] Microsomal lipid peroxidation
Buege, J. A., & Aust, S. D. (1978) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(78)52032-6 · Cited by 13,522
Hydroperoxide metabolism in mammalian organs.
Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827
Oxygen-Derived Free Radicals in Postischemic Tissue Injury
Epstein, F. H., & McCord, J. M. (1985) · New England Journal of Medicine · doi:10.1056/nejm198501173120305 · Cited by 5,399
Harman, D. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.11.7124 · Cited by 1,915
Korshunov, S. S., Skulachev, V. P., & Starkov, A. A. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)01159-9 · Cited by 1,727
Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria
Turrens, J. F., & Boveris, A. (1980) · Biochemical Journal · doi:10.1042/bj1910421 · Cited by 1,601
Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria
Turrens, J. F., Alexandre, A., & Lehninger, A. L. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90293-0 · Cited by 1,214
Direct measurement of free radical generation following reperfusion of ischemic myocardium.
Zweier, J. L., Flaherty, J. T., & Weisfeldt, M. L. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.5.1404 · Cited by 1,189
The biochemistry of programmed cell death
Kroemer, G., PETIT, P. X., Zamzami, N., Vayssière, J., & Mignotte, B. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.13.7557017 · Cited by 992
Flagged first, then by citations
Research works printed but not linked: 1
- 10.1139/y59-099 · DOI · Paper page
Cited by
Sorted by citations
Items 201–261 of 261
Feng, L., Liu, W., Yang, J., Wang, Q., & Wen, S. W. (2018) · Medical Science Monitor · doi:10.12659/msm.907578 · Cited by 9
Ryang, J., Liu, F., & Ng, T. B. (2021) · Journal of Food Biochemistry · doi:10.1111/jfbc.13818 · Cited by 8
Wu, P.-Y., Lai, B., Dong, Y. W., Wang, Z.-M., Li, Z., & Zheng, P. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.05.001 · Cited by 8
Hu, M. S., Li, T., Bo, Z., & Xiang, F. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219840987 · Cited by 8
Ding, J., Ji, R., Wang, Z., Jia, Y., Meng, T., Song, X., Gao, J., & He, Q. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1405545 · Cited by 7
Losito, I., Conte, E., Introna, B., Megli, F. M., & Palmisano, F. (2011) · Journal of Mass Spectrometry · doi:10.1002/jms.2012 · Cited by 7
Taxol, a Microtubule Stabilizer, Improves Cardiac Contractile Function during Ischemia in vitro
Xiao, J., Zhao, H., Liang, D., Liu, Y., Zhang, H., Liu, Y., Li, J., Peng, L., Zhou, Z.-N., & Chen, Y. (2010) · Pharmacology · doi:10.1159/000292948 · Cited by 7
Tan, C., Zeng, J., Wu, Y., Zhang, J., & Chen, W. (2018) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-018-2235-4 · Cited by 7
Antioxidant Therapy and its Effectiveness in Oxidative Stress‐Mediated Disorders
Iannitti, T., & Palmieri, B. (2011) · Wiley eBooks · doi:10.1002/9781118148143.ch15 · Cited by 7
Molecular basis of residual feed intake in broilers
Prakash, A., SAXENA, V. K., Kumar, G. R., Tomar, S., & Singh, M. K. (2020) · World s Poultry Science Journal · doi:10.1080/00439339.2020.1789534 · Cited by 6
Role of Mitochondrial ROS for Calcium Alternans in Atrial Myocytes
Oropeza‐Almazán, Y., & Blatter, L. A. (2024) · Biomolecules · doi:10.3390/biom14020144 · Cited by 7
A short introduction to acyl-CoA dehydrogenases; deficiencies and novel treatment strategies
Lund, M., Olsen, R. K. J., & Gregersen, N. (2015) · Expert Opinion on Orphan Drugs · doi:10.1517/21678707.2015.1092869 · Cited by 7
Cham, E. D., Peng, T., & Jou, M. (2024) · Biology · doi:10.3390/biology13080639 · Cited by 5
Zhang, J., Gong, L., Zhu, H., Sun, W., Tian, J., Zhang, Y., Liu, Q., Li, X., Zhang, F., Wang, S., et al. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106344 · Cited by 5
Abdul, K. S. M., Han, K., Guerrero, A. B., Wilson, C. N., Kulkarni, A., & Purcell, N. H. (2024) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2024.05.014 · Cited by 4
Biomarkers of Mitochondrial Dysfunction and Toxicity
Palmeira, C. M., Teodoro, J. S., Silva, R., & Rolo, A. P. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814655-2.00055-4 · Cited by 4
Chen, Y., Li, Y., Jia, P., Ji, S., Zhang, H., & Wang, T. Z. (2022) · Antioxidants · doi:10.3390/antiox11040666 · Cited by 4
Woo, K., & Padalhin, A. (2023) · Medical Lasers · doi:10.25289/ml.22.047 · Cited by 5
p66Shc is an apoptotic rheostat whose targeted ROS inhibition improves MI outcomesPreprint
Haslem, L., Hays, J. M., Schmitz, H., Matsuzaki, S., Sjoelund, V. H., Byrum, S. D., Humphries, K. M., Frazer, J. K., Demeler, B., Benbrook, D. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.14.487897 · Cited by 4
Elamipretide in the Management of Barth Syndrome: Current Evidence and a Case Report
Jacob, N., Schecter, D., Marshall, M., Bansal, N., Lamour, J. M., Vernon, H. J., Morava, É., & Elsharkawi, I. (2025) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2025.109220 · Cited by 3
Reactive Oxygen Species (ROS) and Cardiac Ischemia and Reperfusion Injury
Camara, A. K. S., & Stowe, D. F. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_75 · Cited by 3
Generation of free oxygen radicals in heart mitochondria: Effect of hypoxia-reoxygenation
Sviryaeva, I. V., & Ruuge, E. K. (2006) · BIOPHYSICS · doi:10.1134/s0006350906030146 · Cited by 3
Biomarkers of mitochondrial dysfunction and toxicity
Palmeira, C. M., Duarte, F. V., Teodoro, J. S., Varela, A. T. I. F., & Rolo, A. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404630-6.00051-8 · Cited by 3
Lipids in the Assembly of Membrane Proteins and Organization of Protein Supercomplexes
Bogdanov, M. V., Mileykovskaya, E., & Dowhan, W. (2008) · Cited by 4
Mosca, S. M. (2011) · Cited by 2
Phosphorylation Events in Selective Mitophagy: Possible Biochemical Markers?
Zhang, W., Wu, H., Liu, L., Zhu, Y., & Chen, Q. (2013) · Current Pathobiology Reports · doi:10.1007/s40139-013-0033-8 · Cited by 2
Dudognon, T., Guderley, H., Quéré, C., Soudant, P., Racotta, I. S., & Kraffe, E. (2015) · Marine Biology · doi:10.1007/s00227-015-2646-4 · Cited by 2
Carnosine, a therapeutic potential for critical limb ischemic.
Boakye, A. A. (2016) · doi:10.18297/etd/2517 · Cited by 2
ROS, Redox Regulation and Signaling in Cancer Cells
Bansal, M. P. (2023) · Springer eBooks · doi:10.1007/978-981-99-7342-2_1 · Cited by 1
Ischémie-reperfusion myocardique — Aspects physiopathologiques
Coquerel, D., & Tamion, F. (2010) · Réanimation · doi:10.1007/s13546-010-0102-5 · Cited by 1
Zou, J., Ya, Z., Pyykkö, I. V., & Wu, H. (2006) · Journal of Otology · doi:10.1016/s1672-2930(06)50019-4 · Cited by 1
Cortés‐Rojo, C., Estrada‐Villagómez, M. M., Manzo‐Ávalos, S., & Saavedra‐Molina, A. (2009) · Información tecnológica · doi:10.4067/s0718-07642009000200010 · Cited by 1
Hanley, P. J., & Daut, J. (2005) · Cited by 1
Lillo‐Moya, J., Rojas-Solé, C., & Rodrigo, R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-19247-0.00009-6 · Cited by 1
Respiratory Cytochrome Supercomplexes
Lenaz, G., & Genova, M. L. (2016) · Advances in photosynthesis and respiration · doi:10.1007/978-94-017-7481-9_29 · Cited by 1
Respiratory Supercomplexes in Mitochondria
Lenaz, G., Tioli, G., Falasca, A. I., & Genova, M. L. (2017) · Royal Society of Chemistry eBooks · doi:10.1039/9781788010405-00296 · Cited by 1
Chapter 10 The Interaction of Mitochondrial Membranes with Reactive Oxygen and Nitrogen Species
(2008) · Current topics in membranes · doi:10.1016/s1063-5823(08)00210-x · Cited by 1
Effet protecteur du safran contre la cardiotoxicité de la doxorubicine en condition ischémique.
Chahine, N. R. (2014) · theses.fr (ABES) · doi:10.70675/1b5abd84z0a6dz4bfazbbd1z9d5c946d2345 · Cited by 1
Gene Expression and Signaling Pathways in Myocardial Ischemia
Marı́n-Garcı́a, J. (2011) · Springer eBooks · doi:10.1007/978-1-4419-9461-5_14
Flavonoid protection of cardiac cells against ischemia-reperfusion injury
Najafabadi, M. A. (2008) · University Library - University of Saskatchewan (University of Saskatchewan)
Cardiovascular Toxicity of Mitochondrial Origin
Oliveira, P. J., Sardão, V. A., & Wallace, K. B. (2008) · Wiley eBooks · doi:10.1002/9780470372531.ch6
Genetic and Nutritional Preconditioning against Ischemia/Reperfusion Injury
Verweij, M. (2011) · EUR Research Repository (Erasmus University Rotterdam)
The Protective Effect of Melatonin on the Heart
Lochner, A. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-600-9_27
de Hidalgo, S. N., & Farmacobiología, F. D. Q. (2010)
Effect of Remote Ischemic Conditioning in Hemorrhagic Shock/Resuscitation
Leung, C. H. (2019) · TSpace (University of Toronto)
Two-Faced Role of ROS in the Regulation of Cancer Cell Signaling
Banudevi, S. (2021) · Springer eBooks · doi:10.1007/978-981-15-4501-6_82-1
Cardiolipin Metabolism in Experimental and Human Heart Failure
Hatch, G. M. (2011) · Springer eBooks · doi:10.1007/978-1-4419-7130-2_13
Mridula, M., Ansary, P. Y., Oommen, S. M., Shincymol, V. V., & Sethu, R. (2021) · International Research Journal of Ayurveda & Yoga · doi:10.47223/irjay.2021.41120
Two-Faced Role of ROS in the Regulation of Cancer Cell Signaling
Banudevi, S. (2022) · Springer eBooks · doi:10.1007/978-981-15-9411-3_82
Kumar, S., Shabeer, A., Rashid, F., Mawlong, I., Rani, R., Singh, V. V., Mog, B., & Pillai, M. (2024) · Emirates Journal of Food and Agriculture · doi:10.3897/ejfa.2024.118303
Interplay Between Autophagy and Reactive Oxygen Species (ROS)
Karwal, A., Pathak, A., Mohan, K. M. G., Jain, V. K., Popli, H., Yadav, A. K., & Jain, K. (2024) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-031-66421-2_6
Ajij, T., Begum, S. A., Mitra, A., & Biswas, S. (2026) · International Journal of Research in Medical Sciences · doi:10.18203/2320-6012.ijrms20260277
Etude de la cardioprotection contre l'infarctus du myocarde au cours de l'obésité expérimentale
Bouhidel, J. O. (2010) · theses.fr (ABES) · doi:10.70675/6ad8f864zee3fz4749za1d1z550c6bf7007c
Développement de stratégies naturelles de cardioprotection : Quel rôle pour la mitochondries ?
Boulghobra, D. (2021) · theses.fr (ABES) · doi:10.70675/72de819azc0ebz4134zb302zc979b24377d3
Innovative multidrug nanomedicines for the treatment of myocardial ischemia/ reperfusion injuries
Tran, N. L. L. (2024) · theses.fr (ABES) · doi:10.70675/a1298b36zf141z401ez87d9z4d42fc1663fd
Oxidative Stress in Cardiovascular Disease: Potential Biomarkers and Their Measurements
Mukherjee, S., & Das, D. K. (2011) · Humana Press eBooks · doi:10.1007/978-1-60761-956-7_6
Metadata
- Authors
- Petrosillo, G., Francesca, M. R., Di Venosa, N., & Paradies, A. G.
- Affiliations
- University of Bari Aldo Moro (IT)
- Department of Emergency and Transplantation University of Bari Bari Italy
- Department of Biochemistry and Molecular Biology CNR Unit for the Study of Mitochondria and Bioenergetics University of Bari Bari Italy
- ORCID
- Petrosillo, Giuseppe
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 2003-02-05
- Volume
- 17
- Issue
- 6
- Pages
- 714-716
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W2158719453
- Cited by
- 261
- References
- 50
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 7 · 2023: 5 · 2022: 11 · 2021: 9 · 2020: 7 · 2019: 11 · 2018: 9 · 2017: 12 · 2016: 13 · 2015: 13 · 2014: 10 · 2013: 14 · 2012: 17
- FWCI
- 7.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The FASEB Journal (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Consiglio Nazionale delle Ricerche
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Ischemia and Reperfusion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- cytochrome bc1 complex, mitochondrial respiratory chain, ischemia-reperfusion injury, cardiolipin, reactive oxygen species, hydrogen peroxide, lipid peroxidation, state 3 respiration, heart mitochondria, oxidative damage
- MeSH terms
- Animals, Cardiolipins, Hydrogen Peroxide, Mitochondria, Heart, Phospholipids, Electron Transport Complex III, Myocardial Reperfusion Injury, Myocardial Ischemia, Reactive Oxygen Species, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review