Mitochondrial dynamics: orchestrating the journey to advanced age
Abstract
Aging is a degenerative process that unfortunately is an inevitable part of life and risk factor for cardiovascular disease including heart failure. Among the several theories purported to explain the effects of age on cardiac dysfunction, the mitochondrion has emerged a central regulator of this process. Hence, it is not surprising that abnormalities in mitochondrial quality control including biogenesis and turnover have such detrimental effects on cardiac function. In fact mitochondria serve as a conduit for biological signals for apoptosis, necrosis and autophagy respectively. The removal of damaged mitochondria by autophagy/mitophagy is essential for mitochondrial quality control and cardiac homeostasis. Defects in mitochondrial dynamism fission/fusion events have been linked to cardiac senescence and heart failure. In this review we discuss the impact of aging on mitochondrial dynamics and senescence on cardiovascular health. This article is part of a Special Issue entitled: CV Aging.
Integrity signals
Registry
Cites
Statistics
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?
Defects in mitochondrial fusion/fission dynamics are essential for the quality control of mitochondria in many age-related diseases, as in cardiac homeostasis and senescence.
“In other organs, defects in mitochondrial fusion/fission dynamics are also essential for the quality control of mitochondria in many age-related diseases as in the case of cardiac homeostasis and senescence (Biala et al., 2015)”
From Mitochondrial Activity and Dynamics Changes Regarding Metabolism in Ageing and Obesity (2017) · cites this paper as Biala et al., 2015
Cites
1 retracted
Das, S., Mitrovsky, G., Vasanthi, H. R., & Das, D. K. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/345105 · Cited by 173 · see citing works
RetractedMitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2014) · Physiological Reviews · doi:10.1152/physrev.00026.2013 · Cited by 5,383 · see citing works
Premature ageing in mice expressing defective mitochondrial DNA polymerase
Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature · doi:10.1038/nature02517 · Cited by 2,734 · see citing works
Chen, H., Detmer, S. A., Ewald, A. J., Griffin, E. E., Fraser, S. E., & Chan, D. C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211046 · Cited by 2,601 · see citing works
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., et al. (2005) · Science · doi:10.1126/science.1112125 · Cited by 2,165 · see citing works
Extension of murine life span by overexpression of catalase targeted to mitochondria
Schriner, S. E., Linford, N. J., Martin, G. M., Treuting, P., Ogburn, C. E., Emond, M., Coskun, P. E., Ladiges, W., Wolf, N., Van Remmen, H., et al. (2005) · Science · doi:10.1126/science.1106653 · Cited by 1,724 · see citing works
Role of the INK4a Locus in Tumor Suppression and Cell Mortality
Serrano, M., Lee, H.-W., Chin, L., Cordon-Cardo, C., Beach, D., & DePinho, R. A. (1996) · Cell · doi:10.1016/s0092-8674(00)81079-x · Cited by 1,585 · see citing works
Mitochondrial Transport of Cations: Channels, Exchangers, and Permeability Transition
Bernardi, P. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.4.1127 · Cited by 1,534 · see citing works
Oxygen, oxidative stress, hypoxia, and heart failure
Giordano, F. J. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24408 · Cited by 1,494 · see citing works
Disruption of Fusion Results in Mitochondrial Heterogeneity and Dysfunction
Chen, H., Chomyn, A., & Chan, D. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503062200 · Cited by 1,376 · cited 1× · see citing works
“are maintained within the cell for mitochondrial biogenesis [24–28].”
BackgroundPINK1-Phosphorylated Mitofusin 2 Is a Parkin Receptor for Culling Damaged Mitochondria
Chen, Y., & Dorn, G. W. (2013) · Science · doi:10.1126/science.1231031 · Cited by 1,323 · see citing works
Nix is a selective autophagy receptor for mitochondrial clearance
Novak, I., Kirkin, V., McEwan, D. G., Zhang, J., Wild, P., Rozenknop, A., Rogov, V., Löhr, F., Popovic, D., Occhipinti, A., et al. (2010) · The EMBO Reports · doi:10.1038/embor.2009.256 · Cited by 1,309 · see citing works
Mammalian sirtuins—emerging roles in physiology, aging, and calorie restriction
Haigis, M. C., & Guarente, L. P. (2006) · Genes & Development · doi:10.1101/gad.1467506 · Cited by 1,295 · see citing works
Ishihara, N., Nomura, M., Jofuku, A., Kato, H., Suzuki, S. O., Masuda, K., Otera, H., Nakanishi, Y., Nonaka, I., Goto, Y.-I., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1907 · Cited by 1,066 · see citing works
Endothelial Cell Senescence in Human Atherosclerosis: Role of Telomere in Endothelial Dysfunction
Minamino, T., Miyauchi, H., Yoshida, T., Ishida, Y., Yoshida, H., & Komuro, I. (2002) · Circulation · doi:10.1161/01.cir.0000013836.85741.17 · Cited by 1,061 · see citing works
Yoon, Y., Krueger, E. W., Oswald, B. J., & McNiven, M. A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.15.5409-5420.2003 · Cited by 820 · see citing works
Properties of the Permeability Transition Pore in Mitochondria Devoid of Cyclophilin D
Basso, E., Fante, L., Fowlkes, J., Petronilli, V., Forte, M. A., & Bernardi, P. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.c500089200 · Cited by 808 · see citing works
Zhao, K., Zhao, G.-M., Wu, D., Soong, Y., Birk, A. V., Schiller, P. W., & Szeto, H. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402999200 · Cited by 782 · see citing works
Mitochondrial Morphology and Dynamics in Yeast and Multicellular Eukaryotes
Okamoto, K., & Shaw, J. M. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.38.072902.093019 · Cited by 737 · see citing works
Sirtuin 1 and Sirtuin 3: Physiological Modulators of Metabolism
Nogueiras, R., Habegger, K. M., Chaudhary, N., Finan, B., Banks, A. S., Dietrich, M. O., Horváth, T. L., Sinclair, D. A., Pfluger, P. T., & Tschöp, M. H. (2012) · Physiological Reviews · doi:10.1152/physrev.00022.2011 · Cited by 712 · see citing works
Calorie restriction and aging: review of the literature and implications for studies in humans
Heilbronn, L. K., & Ravussin, E. (2003) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/78.3.361 · Cited by 701 · see citing works
hFis1, a Novel Component of the Mammalian Mitochondrial Fission Machinery
James, D. I., Parone, P. A., Mattenberger, Y., & Martinou, J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303758200 · Cited by 653 · see citing works
Telomere length and replicative aging in human vascular tissues.
Chang, E., & Harley, C. B. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.24.11190 · Cited by 635 · see citing works
Free Radical Theory of Aging: An Update: Increasing the Functional Life Span
HARMAN, D. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1354.003 · Cited by 601 · see citing works
Tissue-specific regulation of SIRT1 by calorie restriction
Chen, D., Bruno, J., Easlon, E., Lin, S.-J., Cheng, H.-L., Alt, F. W., & Guarente, L. (2008) · Genes & Development · doi:10.1101/gad.1650608 · Cited by 567 · see citing works
Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production
Trifunovic, A., Hansson, A., Wredenberg, A., Rovio, A. T., Dufour, E., Khvorostov, I., Spelbrink, J. N., Wibom, R., Jacobs, H. T., & Larsson, N.-G. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508886102 · Cited by 555 · see citing works
Oxidants in mitochondria: from physiology to diseases
Richter, C., Gogvadze, V. G., Laffranchi, R., Schlapbach, R., Schweizer, M., Suter, M., Walter, P. B., & Yaffee, M. (1995) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/0925-4439(95)00012-s · Cited by 543 · see citing works
Hafner, A. V., Dai, J., Gomes, A. P., Xiao, C., Palmeira, C. M., Rosenzweig, A., & Sinclair, D. A. (2010) · Aging · doi:10.18632/aging.100252 · Cited by 542 · see citing works
Akt activates the mammalian target of rapamycin by regulating cellular ATP level and AMPK activity
Hahn-Windgassen, A., Nogueira, V., Chen, C.-C., Skeen, J. E., Sonenberg, N., & Hay, N. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502876200 · Cited by 539 · see citing works
Adriamycin-induced heart failure: mechanisms and modulation
Singal, P., Li, T.-M., Kumar, D., Danelisen, I., & Iliskovic, N. (2000) · Molecular and Cellular Biochemistry · doi:10.1023/a:1007094214460 · Cited by 464 · see citing works
Mitochondria and Cardiovascular Aging
Dai, D., Rabinovitch, P. S., & Ungvari, Z. I. (2012) · Circulation Research · doi:10.1161/circresaha.111.246140 · Cited by 435 · see citing works
Mitochondrial fission in apoptosis, neurodegeneration and aging
Bossy‐Wetzel, E., Barsoum, M. J., Godzik, A., Schwarzenbacher, R., & Lipton, S. A. (2003) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2003.10.015 · Cited by 428 · see citing works
Jin, S. M., & Youle, R. J. (2013) · Autophagy · doi:10.4161/auto.26122 · Cited by 411 · see citing works
Lee, Y., Lee, H.-Y., Hanna, R. A., & Gustafsson, Å. B. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00368.2011 · Cited by 398 · see citing works
Wohlgemuth, S. E., Seo, A. Y., Marzetti, E., Lees, H. A., & Leeuwenburgh, C. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2009.11.002 · Cited by 397 · see citing works
Sir2 Blocks Extreme Life-Span Extension
Fabrizio, P., Gattazzo, C., Battistella, L., Wei, M., Cheng, C., McGrew, K., & Longo, V. D. (2005) · Cell · doi:10.1016/j.cell.2005.08.042 · Cited by 388 · see citing works
Telomeres, Telomerase, and Immortality
Rhyu, M. S. (1995) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/87.12.884 · Cited by 388 · see citing works
Haendeler, J., Hoffmann, J., Diehl, J. F., Vasa‐Nicotera, M., Spyridopoulos, I., Zeiher, A. M., & Dimmeler, S. (2004) · Circulation Research · doi:10.1161/01.res.0000121104.05977.f3 · Cited by 382 · see citing works
Seven sirtuins for seven deadly diseases ofaging
Morris, B. J. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.10.525 · Cited by 380 · see citing works
Tanno, M., Kuno, A., Yano, T., Miura, T., Hisahara, S., Ishikawa, S., Shimamoto, K., & Horio, Y. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.090266 · Cited by 358 · see citing works
Wu, J., Liu, J., Chen, E. B., Wang, J., Cao, L., Narayan, N., Fergusson, M. M., Rovira, I. I., Allen, M. D., Springer, D., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.07.030 · Cited by 328 · see citing works
Leri, A., Franco, S., Zacheo, A., Barlucchi, L., Chimenti, S., Limana, F., Nadal‐Ginard, B., Kajstura, J., Anversa, P., & Blasco, M. A. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg013 · Cited by 313 · see citing works
Chiara, F., Castellaro, D., Marin, O., Petronilli, V., Brusilow, W. S. A., Juhaszova, M., Sollott, S. J., Forte, M. A., Bernardi, P., & Rasola, A. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001852 · Cited by 291 · see citing works
Alavi, M. V., Bette, S. J., Schimpf, S., Schuettauf, F., Schraermeyer, U., Wehrl, H. F., Rüttiger, L., Beck, S. C., Tonagel, F., Pichler, B. J., et al. (2006) · Brain · doi:10.1093/brain/awm005 · Cited by 278 · see citing works
Metabolic analysis of senescent human fibroblasts reveals a role for AMP in cellular senescence
Zwerschke, W., Mazurek, S., Stöckl, P., Hütter, E., EIGENBRODT, E., & Jansen‐Dürr, P. (2003) · Biochemical Journal · doi:10.1042/bj20030816 · Cited by 248 · see citing works
Park, Y.-Y., Lee, S., Karbowski, M., Neutzner, A., Youle, R. J., & Cho, H. (2010) · Journal of Cell Science · doi:10.1242/jcs.061481 · Cited by 244 · see citing works
Mitochondrial dynamics and disease, OPA1
Olichon, A., Guillou, E., Delettre, C., Landes, T., Pelloquin, L., Emorine, L. J., Mils, V., Daloyau, M., Hamel, C., Amati‐Bonneau, P., et al. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.04.003 · Cited by 238 · see citing works
Disturbed Flow Promotes Endothelial Senescence via a p53-Dependent Pathway
Warboys, C. M., de Luca, A., Amini, N., Luong, L., Duckles, H., Hsiao, S., White, A., Biswas, S., Khamis, R., Chong, C. K., et al. (2014) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.114.303415 · Cited by 227 · see citing works
Contribution of Impaired Mitochondrial Autophagy to Cardiac Aging
Dutta, D., Calvani, R., Bernabei, R., Leeuwenburgh, C., & Marzetti, E. (2012) · Circulation Research · doi:10.1161/circresaha.111.246108 · Cited by 221 · see citing works
Physiological functions of mitochondrial fusion
Chen, H., & Chan, D. C. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05615.x · Cited by 221 · see citing works
Dhingra, R., Margulets, V., Chowdhury, S. R., Thliveris, J. A., Jassal, D. S., Fernyhough, P., Dorn, G. W., & Kirshenbaum, L. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414665111 · Cited by 217 · see citing works
Self-citationRole of p14<sup>ARF</sup> in Replicative and Induced Senescence of Human Fibroblasts
Wei, W., Hemmer, R. M., & Sedivy, J. M. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.20.6748-6757.2001 · Cited by 217 · see citing works
Antioxidant Defenses in the Lung
Fridovich, I., & Freeman, B. E. (1986) · Annual Review of Physiology · doi:10.1146/annurev.ph.48.030186.003401 · Cited by 213 · see citing works
SIRT3 deficiency exacerbates ischemia-reperfusion injury: implication for aged hearts
Porter, G. A., Jr., Urciuoli, W. R., Brookes, P. S., & Nadtochiy, S. M. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00027.2014 · Cited by 212 · see citing works
Cellular Senescence, Vascular Disease, and Aging
Kovacic, J. C., Moreno, P., Hachinski, V., Nabel, E. G., & Fuster, V. (2011) · Circulation · doi:10.1161/circulationaha.110.007021 · Cited by 205 · see citing works
Ishihara, T., Ban-Ishihara, R., Maeda, M., Matsunaga, Y., Ichimura, A., Kyogoku, S., Aoki, H., Katada, S., Nakada, K., Nomura, M., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01054-14 · Cited by 194 · see citing works
Effects of Age and Heart Failure on Human Cardiac Stem Cell Function
Cesselli, D., Beltrami, A. P., D’Aurizio, F., Marcon, P., Bergamin, N., Toffoletto, B., Pandolfi, M., Puppato, E., Marino, L., Signore, S., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.03.036 · Cited by 190 · see citing works
Gano, L. B., Donato, A. J., Pasha, H. M., Hearon, C. M., Sindler, A. L., & Seals, D. R. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00377.2014 · Cited by 188 · see citing works
The Mitochondrial Dynamism-Mitophagy-Cell Death Interactome
Dorn, G. W., & Kitsis, R. N. (2014) · Circulation Research · doi:10.1161/circresaha.116.303554 · Cited by 185 · see citing works
Joseph, A.-M., Adhihetty, P. J., Wawrzyniak, N. R., Wohlgemuth, S. E., Picca, A., Kujoth, G. C., Prolla, T. A., & Leeuwenburgh, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069327 · Cited by 161 · see citing works
Bhandari, P., Song, M., Chen, Y., Burelle, Y., & Dorn, G. W. (2013) · Circulation Research · doi:10.1161/circresaha.114.302734 · Cited by 153 · see citing works
Westhoff, J. H., Hilgers, K. F., Steinbach, M. P., Hartner, A., Klanke, B., Amann, K., & Melk, A. (2008) · Hypertension · doi:10.1161/hypertensionaha.107.099432 · Cited by 152 · see citing works
Superoxide Radical: Controversies, Contradictions, and Paradoxes
McCord, J. M. (1995) · Experimental Biology and Medicine · doi:10.3181/00379727-209-43885c · Cited by 150 · see citing works
Expression of Chr9p21 genes CDKN2B (p15), CDKN2A (p16, p14) and MTAP in human atherosclerotic plaque
Holdt, L. M., Sass, K., Gäbel, G., Bergert, H., Thiery, J., & Teupser, D. (2011) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2010.06.029 · Cited by 143 · see citing works
Chen, J., Huang, X., Halicka, D., Brodsky, S., Avram, A., Eskander, J., Bloomgarden, N. A., Darzynkiewicz, Z., & Goligorsky, M. S. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00364.2005 · Cited by 142 · see citing works
Voghel, G., Thorin‐Trescases, N., Farhat, N., Nguyen, A. Q., Villeneuve, L. R., Mamarbachi, A. M., Fortier, A., Perrault, L. P., Carrier, M., & Thorin, É. (2007) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2007.09.006 · Cited by 141 · see citing works
MARF and Opa1 Control Mitochondrial and Cardiac Function in Drosophila
Dorn, G. W., Clark, C. F., Eschenbacher, W. H., Kang, M., Engelhard, J. T., Warner, S. J., Matkovich, S. J., & Jowdy, C. C. (2010) · Circulation Research · doi:10.1161/circresaha.110.236745 · Cited by 136 · see citing works
Senescence-Induced Oxidative Stress Causes Endothelial Dysfunction
Bhayadia, R., Schmidt, B. M. W., Melk, A., & Hömme, M. (2016) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glv008 · Cited by 126 · see citing works
Construction of transgenic mice with tissue-specific acceleration of mitochondrial DNA mutagenesis
Zhang, D., Mott, J. L., Chang, S.-W., Denniger, G., Feng, Z., & Zassenhaus, H. P. (2000) · Genomics · doi:10.1006/geno.2000.6333 · Cited by 124 · see citing works
A relative deficit in antioxidant reserve may contribute in cardiac failure.
Singal, P. K., & Kirshenbaum, L. A. (1990) · PubMed · Cited by 120 · see citing works
Self-citationFerree, A. W., Trudeau, K. M., Zik, E., Benador, I. Y., Twig, G., Gottlieb, R. A., & Shirihai, O. S. (2013) · Autophagy · doi:10.4161/auto.26503 · Cited by 119 · see citing works
Feuerstein, G., Yue, T., Ma, X., & Ruffolo, R. R., Jr. (1998) · Progress in Cardiovascular Diseases · doi:10.1016/s0033-0620(98)80027-3 · Cited by 117 · see citing works
Wei, Y., Wu, S., Ma, Y., & Lee, H. (2009) · PubMed · Cited by 113 · see citing works
Deceleration of Fusion–Fission Cycles Improves Mitochondrial Quality Control during Aging
Figge, M. T., Reichert, A. S., Meyer‐Hermann, M., & Osiewacz, H. D. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002576 · Cited by 112 · see citing works
Giedt, R. J., Yang, C., Zweier, J. L., Anastasios Matzavinos, A., & Alevriadou, B. R. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.10.491 · Cited by 111 · see citing works
Franco, S. S., Falco, L. D., Ghaffari, S., Brugnara, C., Sinclair, D. A., Mattè, A., Iolascon, A., Mohandas, N., Bertoldi, M., An, X., et al. (2013) · Haematologica · doi:10.3324/haematol.2013.090076 · Cited by 109 · see citing works
Myocardial Aging and Senescence: Where Have the Stem Cells Gone?
Sussman, M. A., & Anversa, P. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.032102.140723 · Cited by 108 · see citing works
Telomerase Activity in Rat Cardiac Myocytes is Age and Gender Dependent
Leri, A., Malhotra, A., Liew, C., Kajstura, J., & Anversa, P. (2000) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1999.1084 · Cited by 89 · see citing works
Atkins, K. M., Thomas, L. L., González, J. B., Thomas, L., Auclair, S., Yin, J., Kang, H., Chung, J. H., Dikeakos, J. D., & Thomas, G. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.049 · Cited by 87 · see citing works
Zhao, L., Zou, X., Feng, Z., Luo, C., Liu, J., Li, H., Chang, L., Wang, H., Li, Y., Long, J., et al. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.001 · Cited by 86 · see citing works
p53 Mediates Autophagy and Cell Death by a Mechanism Contingent On Bnip3
Wang, E. Y., Gang, H., Aviv, Y., Dhingra, R., Margulets, V., & Kirshenbaum, L. A. (2013) · Hypertension · doi:10.1161/hypertensionaha.113.01028 · Cited by 84 · see citing works
Self-citationDorn, G. W., & Scorrano, L. (2010) · Circulation Research · doi:10.1161/circresaha.110.225714 · Cited by 80 · see citing works
Autophagy and mitophagy in the myocardium: therapeutic potential and concerns
Jimenez, R. E., Kubli, D. A., & Gustafsson, Å. B. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12477 · Cited by 76 · see citing works
Mitochondrial Fission and Autophagy in the Normal and Diseased Heart
Iglewski, M., Hill, J. A., Lavandero, S., & Rothermel, B. A. (2010) · Current Hypertension Reports · doi:10.1007/s11906-010-0147-x · Cited by 72 · see citing works
Luo, X.-Y., Qu, S.-L., Tang, Z., Zhang, Y. E., Liu, M., Peng, J., Tang, H. R., Yu, K., Zhang, C., Ren, Z., et al. (2014) · Clinica Chimica Acta · doi:10.1016/j.cca.2014.07.019 · Cited by 72 · see citing works
The role of calorie restriction and SIRT1 in prion-mediated neurodegeneration
Chen, D., Steele, A. D., Hütter, G., Bruno, J., Govindarajan, A., Easlon, E. J., Lin, S.-J., Aguzzi, A., Lindquist, S. L., & Guarente, L. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.08.050 · Cited by 71 · see citing works
Tam, Z. Y., Gruber, J., Halliwell, B. B., & Gunawan, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076230 · Cited by 71 · see citing works
Striking a Balance: Autophagy, Apoptosis, and Necrosis in a Normal and Failing Heart
Mughal, W., Dhingra, R., & Kirshenbaum, L. A. (2012) · Current Hypertension Reports · doi:10.1007/s11906-012-0304-5 · Cited by 67 · see citing works
Self-citationLoss of Drp1 function alters OPA1 processing and changes mitochondrial membrane organization
Möpert, K., Hajek, P., Frank, S., Chen, C. I.-U., Kaufmann, J., & Santel, A. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.04.016 · Cited by 66 · see citing works
Naoi, M., Maruyama, W., & Inaba-Hasegawa, K. (2012) · Current Topics in Medicinal Chemistry · doi:10.2174/156802612805219950 · Cited by 65 · see citing works
Pohjoismäki, J., Boettger, T., Liu, Z., Goffart, S., Szibor, M., & Braun, T. W. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks301 · Cited by 65 · see citing works
Age-associated stresses induce an anti-inflammatory senescent phenotype in endothelial cells
Coleman, P. R., Chang, G., Hutás, G., Grimshaw, M. J., Vadas, M. A., & Gamble, J. R. (2013) · Aging · doi:10.18632/aging.100622 · Cited by 60 · see citing works
Dhingra, R., Gang, H., Wang, E. Y., Biala, A. K., Aviv, Y., Margulets, V., Tee, A. R., & Kirshenbaum, L. A. (2013) · Circulation Heart Failure · doi:10.1161/circheartfailure.112.000061 · Cited by 53 · see citing works
Self-citationKraytsberg, Y., Nekhaeva, E., Bodyak, N. B., & Khrapko, K. (2003) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(02)00169-0 · Cited by 52 · see citing works
Cardiac reanimation: targeting cardiomyocyte death by BNIP3 and NIX/BNIP3L
Dorn, G. W., & Kirshenbaum, L. A. (2008) · Oncogene · doi:10.1038/onc.2009.53 · Cited by 51 · see citing works
Self-citationThe anti-aging, metabolism potential of SIRT1.
Ghosh, H. S. (2008) · PubMed · Cited by 49 · see citing works
Jadiya, P., Chatterjee, M., Sammi, S. R., Kaur, S., Palit, G., & Nazir, A. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.08.092 · Cited by 49 · see citing works
Antioxidant changes in heart hypertrophy: significance during hypoxia–reoxygenation injury
Kirshenbaum, L. A., & Singal, P. K. (1992) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y92-186 · Cited by 45 · see citing works
Self-citationAge-dependent mitochondrial energy dynamics in the mice heart: Role of superoxide dismutase-2
Das, K. C., & Muniyappa, H. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.06.002 · Cited by 39 · see citing works
Rohrbach, S., Aslam, M., Niemann, B., & Schulz, R. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12650 · Cited by 30 · see citing works
NADH oxidase activity of Bacillus subtilis nitroreductase NfrA1: Insight into its biological role
Cortial, S., Chaignon, P., Iorga, B. I., Aymerich, S., Truan, G., Gueguen‐Chaignon, V., Meyer, P., Moréra, S., & Ouazzani, J. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.08.019 · Cited by 30 · see citing works
Eschenbacher, W. H., Song, M., Chen, Y., Bhandari, P., Zhao, P. Y., Jowdy, C. C., Engelhard, J. T., & Dorn, G. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044296 · Cited by 29 · see citing works
Detoxifying function of cytochrome c against oxygen toxicity
Lee, M., & Xu, J.-X. (2006) · Mitochondrion · doi:10.1016/j.mito.2006.11.011 · Cited by 29 · see citing works
Johnson, D., Allman, E. L., & Nehrke, K. W. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00411.2011 · Cited by 25 · see citing works
Katada, S., Mito, T., Ogasawara, E., Hayashi, J., & Nakada, K. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.007245 · Cited by 19 · see citing works
Nix Nought Nothing: Fairy tale or real deal
Dorn, G. W. (2010) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2010.09.011 · Cited by 16 · see citing works
Mst-1 switches between cardiac cell life and death
Dhingra, R., & Kirshenbaum, L. A. (2013) · Nature Medicine · doi:10.1038/nm.3371 · Cited by 10 · see citing works
Self-citationChapter 16 Dissecting Apoptosis and Intrinsic Death Pathways in the Heart
Weidman, D. R., Shaw, J., Bednarczyk, J. M., Regula, K. M., Yurkova, N., Zhang, T., Aguilar, F., & Kirshenbaum, L. A. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(08)01616-9 · Cited by 9 · see citing works
Self-citation
Flagged first, then by citations
2 of the 110 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Proteasomal and Autophagic Degradation Systems
Đikić, I. (2017) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-061516-044908 · Cited by 1,165 · see citing works
ROS, Cell Senescence, and Novel Molecular Mechanisms in Aging and Age‐Related Diseases
Davalli, P., Mitic, T., Caporali, A., Lauriola, A., & D’Arca, D. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/3565127 · Cited by 1,059 · see citing works
Oxidative Stress in Human Pathology and Aging: Molecular Mechanisms and Perspectives
Hajam, Y. A., Rani, R., Ganie, S. Y., Sheikh, T. A., Javaid, D., Qadri, S. S., Pramodh, S., Alsulimani, A., Alkhanani, M. F., Harakeh, S., et al. (2022) · Cells · doi:10.3390/cells11030552 · Cited by 915 · see citing works
Mitochondrial function as a therapeutic target in heart failure
Brown, D. A., Perry, J. B., Allen, M. E., Sabbah, H. N., Stauffer, B. L., Shaikh, S. R., Cleland, J. G. F., Colucci, W. S., Butler, J., Voors, A. A., et al. (2016) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2016.203 · Cited by 811 · see citing works
Biczo, G., Vegh, E. T., Shalbueva, N., Mareninova, O. A., Elperin, J., Lotshaw, E., Gretler, S., Lugea, A., Malla, S. R., Dawson, D., et al. (2018) · Gastroenterology · doi:10.1053/j.gastro.2017.10.012 · Cited by 406 · see citing works
Mitochondrial function in hypoxic ischemic injury and influence of aging
Ham, P. B., & Raju, R. P. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.06.006 · Cited by 367 · see citing works
Regulation of SIRT1 in aging: Roles in mitochondrial function and biogenesis
Yuan, Y., Cruzat, V. F., Newsholme, P., Cheng, J., Chen, Y., & Lu, Y. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.02.003 · Cited by 301 · see citing works
Quercetin and the mitochondria: A mechanistic view
de Oliveira, M. R., Nabavi, S. M., Braidy, N., Setzer, W. N., Ahmed, T., & Nabavi, S. F. (2015) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.12.014 · Cited by 252 · see citing works
So! What's aging? Is cardiovascular aging a disease?
Lakatta, E. G. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.04.005 · Cited by 221 · see citing works
Targeting Mitochondrial Biogenesis with Polyphenol Compounds
Chodari, L., Aytemir, M. D., Vahedi, P., Alipour, M., Vahed, S. Z., Khatibi, S. M. H., Ahmadian, E., Ardalan, M., & Eftekhari, A. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/4946711 · Cited by 194 · see citing works
Mitochondrial fission and fusion
Lee, H., & Yoon, Y. (2016) · Biochemical Society Transactions · doi:10.1042/bst20160129 · Cited by 183 · see citing works
Sex Differences in the Biology and Pathology of the Aging Heart
Keller, K. M., & Howlett, S. E. (2016) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2016.03.017 · Cited by 152 · see citing works
SIRT4 interacts with OPA1 and regulates mitochondrial quality control and mitophagy
Lang, A., Anand, R., Altinoluk-Hambüchen, S., Ezzahoini, H., Stefanski, A., Iram, A., Bergmann, L., Urbach, J., Böhler, P., Hänsel, J., et al. (2017) · Aging · doi:10.18632/aging.101307 · Cited by 145 · see citing works
Doxorubicin‐Induced Cardiomyopathy in Children
Mancilla, T. R., Iskra, B., & Aune, G. J. (2019) · Comprehensive Physiology · doi:10.1002/cphy.c180017 · Cited by 108 · see citing works
Tong, W., Ju, L., Qiu, M., Xie, Q., Chen, Y., Shen, W., Sun, W., Wang, W., & Tian, J. (2015) · Hepatology Research · doi:10.1111/hepr.12634 · Cited by 107 · see citing works
Mitochondrial Activity and Dynamics Changes Regarding Metabolism in Ageing and Obesity
López-Lluch, G. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.12.005 · Cited by 103 · see citing works
“…defects in mitochondrial fusion/fission dynamics are also essential for the quality control of mitochondria in many age-related diseases as in the case of cardiac homeostasis and senescence (Biala et al., 2015), or in neurodegeneration and hypothalamic dysfunction (Zorzano and Claret, 2015).”
BackgroundInfluentialPattaro, C., Gögele, M., Mascalzoni, D., Melotti, R., Schwienbacher, C., Grandi, A. D., Foco, L., D’Elia, Y., Linder, B., Fuchsberger, C., et al. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-015-0704-9 · Cited by 103 · see citing works
Li, Y., Ma, Y., Song, L., Yu, L., Zhang, L., Zhang, Y., Xing, Y., Yin, Y., & Ma, H. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3555 · Cited by 98 · see citing works
You, Y., Chen, X., Chen, Y., Pang, J., Chen, Q., Liu, Q., Xue, H., Zeng, Y., Xiao, J., Mi, J., et al. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102828 · Cited by 92 · see citing works
Towards a unified mechanistic theory of aging
Barja, G. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.05.016 · Cited by 88 · see citing works
Salminen, A., Kaarniranta, K., & Kauppinen, A. (2016) · Biogerontology · doi:10.1007/s10522-016-9655-7 · Cited by 86 · see citing works
Mitochondrial quality control: The role of mitophagy in aging
Shi, R., Guberman, M., & Kirshenbaum, L. A. (2017) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2017.11.008 · Cited by 84 · see citing works
Self-citationMIRO GTPases in Mitochondrial Transport, Homeostasis and Pathology
Tang, B. L. (2015) · Cells · doi:10.3390/cells5010001 · Cited by 82 · see citing works
Wang, S., Ge, W., Harns, C., Meng, X., Zhang, Y., & Ren, J. T. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.04.009 · Cited by 71 · see citing works
Huang, Y., Lu, L., Zhu, D., Wang, M., Yin, Y., Chen, D., & Wei, L. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/9573291 · Cited by 67 · see citing works
Protein-bound uremic toxins impaired mitochondrial dynamics and functions
Sun, C., Cheng, M., Pan, H., Lee, J.-H., & Lee, C. (2017) · Oncotarget · doi:10.18632/oncotarget.20773 · Cited by 62 · see citing works
Baburamani, A. A., Hurling, C., Stolp, H. B., Sobotka, K. S., Gressèns, P., Hagberg, H., & Thornton, C. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160922509 · Cited by 62 · see citing works
Ioannides, Z. A., Ngo, S. T., Henderson, R. D., McCombe, P., & Steyn, F. J. (2016) · Neurodegenerative Diseases · doi:10.1159/000446502 · Cited by 53 · see citing works
The SUMO protease SENP3 regulates mitochondrial autophagy mediated by Fis1
Waters, E., Wilkinson, K. A., Harding, A. L., Carmichael, R. E., Robinson, D. A., Colley, H. E., & Guo, C. (2022) · EMBO Reports · doi:10.15252/embr.201948754 · Cited by 49 · see citing works
Huang, M., Yang, L., Peng, X., Wei, S., Fan, Q., Yang, S., Li, X., Li, B., Jin, H., Wu, B., et al. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01698-5 · Cited by 52 · see citing works
Aung, L. H. H., Jumbo, J. C. C., Wang, Y., & Li, P. (2021) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2021.06.006 · Cited by 44 · see citing works
Malandraki-Miller, S., Lopez, C. A., Al-Siddiqi, H., & Carr, C. A. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00119 · Cited by 43 · see citing works
Immunometabolism and oxidative stress: roles and therapeutic strategies in cancer and aging
Zhou, N.-J., Bao, W.-Q., Zhang, C., Jiang, M., Liang, T.-L., Ma, G.-Y., Liu, L., Pan, H., & Li, R.-Z. (2025) · npj Aging · doi:10.1038/s41514-025-00250-z · Cited by 44 · see citing works
Mitochondrial-induced Epigenetic Modifications: From Biology to Clinical Translation
Sharma, J., Kumari, R., Bhargava, A., Tiwari, R. R., & Mishra, P. K. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200826165735 · Cited by 32 · see citing works
Mitochondrial DNA mitochondrial dysfunction and cardiac manifestations
Han, J. (2017) · Frontiers in bioscience · doi:10.2741/4541 · Cited by 33 · see citing works
Mitochondrial Mutations in Cardiac Disorders
Lee, S. R., & Han, J. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-55330-6_5 · Cited by 32 · see citing works
AMPK/Mitochondria in Metabolic Diseases
Bullón, P., Marín‐Aguilar, F., & Román-Malo, L. (2016) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-319-43589-3_6 · Cited by 31 · see citing works
Saha, P., Ajgaonkar, S., Maniar, D., Sahare, S., Mehta, D. S., & Nair, S. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1370951 · Cited by 30 · see citing works
Thompson, J., Maceyka, M. W., & Chen, Q. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111380 · Cited by 30 · see citing works
Song, S. B., Park, J., Jang, S. Y., & Hwang, E. S. (2021) · Cells · doi:10.3390/cells10030612 · Cited by 30 · see citing works
Shi, C., Li, Q., & Zhang, X. (2020) · Pharmacology · doi:10.1159/000505593 · Cited by 32 · see citing works
Dhalla, N. S., Ošťádal, P., & Tappia, P. S. (2025) · Biomedicines · doi:10.3390/biomedicines13061338 · Cited by 27 · see citing works
Mitochondrial Aging: Is There a Mitochondrial Clock?
Zorov, D. B., Popkov, V. A., Zorova, L. D., Vorobjev, I. A., Pevzner, I. B., Silachev, D. N., Zorov, S. D., Jankauskas, S. S., Babenko, V. A., & Plotnikov, E. Y. (2016) · The Journals of Gerontology Series A · doi:10.1093/gerona/glw184 · Cited by 27 · see citing works
Valli, H., Ahmad, S., Chadda, K. R., Al-Hadithi, A., Grace, A. A., Jeevaratnam, K., & Huang, C. L.-H. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2017.09.002 · Cited by 25 · see citing works
Paillard, M., Abdellatif, M., Andreadou, I., Bär, C., Bertrand, L., Brundel, B. J. J. M., Chiva‐Blanch, G., Davidson, S. M., Dawson, D. K., Lisa, F. D., et al. (2025) · European Journal of Heart Failure · doi:10.1002/ejhf.3674 · Cited by 28 · see citing works
Kaur, A., Jankowska, K., Pilgrim, C., Fraser, S. T., & New, E. J. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6495 · Cited by 22 · see citing works
Connect and Conquer: Collectivized Behavior of Mitochondria and Bacteria
Williams, C. F., & George, C. H. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00340 · Cited by 21 · see citing works
Mitochondrial Dynamics Impairment in Dexamethasone-Treated Neuronal Cells
Suwanjang, W., Wu, K. L. H., Prachayasittikul, S., Chetsawang, B., & Charngkaew, K. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02779-4 · Cited by 20 · see citing works
Zhou, Y. L., You, H., Zhang, A., Jiang, X., Pu, Z., Xu, G., & Zhao, M. (2020) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2020.8812 · Cited by 18 · see citing works
Huang, L., Chen, R., Liu, L., Zhou, Y., & Chen, Z. (2021) · Food & Function · doi:10.1039/d0fo03346d · Cited by 19 · see citing works
Surai, P. F. (2015) · Journal of Veterinary Science & Medicine · doi:10.13188/2325-4645.1000017 · Cited by 17 · see citing works
Conditioning-induced cardioprotection: Aging as a confounding factor
Randhawa, P. K., Bali, A., Virdi, J. K., & Jaggi, A. S. (2018) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2018.22.5.467 · Cited by 17 · see citing works
Kanoi, R., Loachan, P., Das, S., & Rao, B. S. S. (2021) · Molecular Biology Reports · doi:10.1007/s11033-020-06074-2 · Cited by 17 · see citing works
Ellagic acid inhibits mitochondrial fission protein Drp-1 and cell proliferation in cancer
Yakobov, S., Dhingra, R., Margulets, V., Dhingra, A., Crandall, M., & Kirshenbaum, L. A. (2023) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-022-04627-6 · Cited by 16 · see citing works
Self-citationDoxorubicin‐Induced Cardiomyopathy in Children
Mancilla, T. R., Iskra, B. S., & Aune, G. J. (2019) · Comprehensive physiology · doi:10.1002/j.2040-4603.2019.tb00082.x · Cited by 16 · see citing works
Polyphenol-Based Therapeutic Strategies for Mitochondrial Dysfunction in Aging
Maksimović, T., Gădău, C., Antal, G., Čoban, M., Eșanu, O., Atyim, E., Mioc, A., & Şoica, C. (2025) · Biomolecules · doi:10.3390/biom15081116 · Cited by 15 · see citing works
Future perspectives on the roles of mitochondrial dynamics in the heart in obesity and aging
Maneechote, C., Chattipakorn, S. C., & Chattipakorn, N. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122575 · Cited by 15 · see citing works
Jiménez, R., Zúñiga-Muñoz, A. M., Álvarez-León, E., García‐Niño, W. R., Navarrete-Anastasio, G., Soria‐Castro, E., Pérez-Torres, I., Lira‐Silva, E., Pavón, N., Cruz‐Gregorio, A., et al. (2024) · Biogerontology · doi:10.1007/s10522-024-10174-y · Cited by 15 · see citing works
A Toolbox for Organelle Mechanobiology Research—Current Needs and Challenges
Feng, Q., Lee, S. S., & Kornmann, B. (2019) · Micromachines · doi:10.3390/mi10080538 · Cited by 13 · see citing works
Schilling, J. M., & Patel, H. H. (2015) · The Journal of Physiology · doi:10.1113/jp270591 · Cited by 11 · see citing works
Wendt, L., Vider, J., Hoe, L. E. S., Toit, E. D., Peart, J. N., & Headrick, J. P. (2019) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.119.258897 · Cited by 10 · see citing works
Autophagy of naïve CD4+T cells in aging – the role of body adiposity and physical fitness
Padilha, C. S., Kushkestani, M., Baptista, L. C. P., Krüger, K., & Lira, F. S. (2023) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2023.2 · Cited by 9 · see citing works
mtDNA damage in the development of heart failure
Lombardi, A. A., & Elrod, J. W. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00475.2015 · Cited by 9 · see citing works
Effects of resveratrol on mitochondrial biogenesis and physiological diseases
Uriho, A., Xue Ming, T. A. N. G., Le, G., Yang, S., Harimana, Y., Papy, I. S., Yiping, L., Zhang, K., Ma, S., & Muhoza, B. (2020) · Oriental Pharmacy and Experimental Medicine · doi:10.1007/s13596-020-00492-0 · Cited by 9 · see citing works
Feng, W.-J., Mou, J., Liao, P.-P., Zhou, J., Zhang, N., Hu, T., Wang, S., Zhang, S.-Y., & Mao, Y. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01534-y · Cited by 8 · see citing works
Sarcolemmal dependence of cardiac protection and stress‐resistance: roles in aged or diseased hearts
Hoe, L. E. S., May, L. T., Headrick, J. P., & Peart, J. N. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13552 · Cited by 8 · see citing works
Molecular Biology Digest of Cell Mitophagy
Matić, I., Strobbe, D., Guglielmo, F. D., & Campanella, M. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2016.12.003 · Cited by 7 · see citing works
Frailty and Cardiovascular Disease
Chainani, V., Riehl, R., Chainani, G., Abdo, A., Cohen, M. G., Alfonso, C., Martinez-Clark, P. O., Lavie, C. J., Reilly, J. P., & Abi‐Rafeh, N. (2017) · InTech eBooks · doi:10.5772/intechopen.69877 · Cited by 7 · see citing works
Zhang, S., Gao, Y., & Wang, J. (2017) · PubMed Central · Cited by 6 · see citing works
Xue, Y.-T., Zhang, J., Yan, J., Qiu, J., Zeng, J., Li, Y., Huang, X., Li, X., Li, G., Wu, L., et al. (2025) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2025.107655 · Cited by 5 · see citing works
Sang, J.-J., Gao, J., Zuo, H., Yu, H., Qin, Y., Hu, J., & Hao, F. (2025) · Biomolecules · doi:10.3390/biom15121671 · Cited by 5 · see citing works
Shiitake mushroom powder supplementation increase antioxidative activity in dogs
Kusaba, A., & Arai, T. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1355560 · Cited by 5 · see citing works
Nugraheni, N., & Ahlina, F. N. (2021) · The Thai Journal of Pharmaceutical Sciences · doi:10.56808/3027-7922.2489 · Cited by 5 · see citing works
Surai, P. F. (2015) · Cited by 5 · see citing works
Antioxidants and Polyphenols Mediate Mitochondrial Mediated Muscle Death Signaling in Sarcopenia
Alway, S. E. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-810422-4.00026-9 · Cited by 6 · see citing works
Age-related obesity and inflammaging in cats
Kobayashi, M., & Kobayashi, M. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1639055 · Cited by 2 · see citing works
Mitochondrially-Targeted Ratiometric Redox Probes
Kaur, A. (2018) · Springer theses · doi:10.1007/978-3-319-73405-7_4 · Cited by 1 · see citing works
Linking mitochondrial dysfunction to sarcopenia
Alway, S. E. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822146-4.00004-1 · Cited by 1 · see citing works
The role of mitochondria in the myocardium of senescent Meriones unguiculates
Potapenko, Y., Dyomshina, O. O., & Ушакова, Г. А. (2017) · Regulatory Mechanisms in Biosystems · doi:10.15421/021779
Abdullahi, A., Olaleke, B., Adeyemi, R. O., & Oluwatosin, S. (2020) · Journal of Emerging Technologies and Innovative Research
Defining novel physiological roles for cardiac-residen Macrophages
Ávila, J. Á. N. (2020) · doi:10.4321/repisalud.10674
Protein Phosphatase 2A Orchestrates Mitochondrial Dynamics via MAPK Signaling in heartPreprint
Dong, D., Zhang, Y., Li, L., Fan, H., Jin, T., Gao, X., & Zhang, Z. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.26.708402
- Authors
- Biala, A. K., Dhingra, R., & Kirshenbaum, L. A.
- Affiliations
- St. Boniface Hospital (CA)
- Corresponding author
- Kirshenbaum, Lorrie A.
- Venue
- Journal of Molecular and Cellular Cardiology
- Publisher
- Elsevier BV
- Published
- 2015-06
- Volume
- 83
- Pages
- 37-43
- ISSN
- 0022-2828 (ISSN-L)
- OpenAlex
- W2072541352
- Cited by
- 82
- References
- 110
- Citations by year
- 2026: 1 · 2025: 7 · 2024: 5 · 2023: 3 · 2022: 2 · 2021: 7 · 2020: 8 · 2019: 7 · 2018: 6 · 2017: 12 · 2016: 14 · 2015: 10
- FWCI
- 1.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Molecular and Cellular Cardiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research (MOP42402)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- mitochondrial dynamics, mitochondrial fission, mitochondrial fusion, aging, cardiac senescence, heart failure, mitochondrial quality control, mitophagy, mitochondrial biogenesis, mitochondrial turnover, apoptosis, necrosis, autophagy, cardiovascular aging
- MeSH terms
- Aging, Animals, Gene Expression Regulation, Heart Failure, Humans, Mitochondria, Myocardium, Signal Transduction, Cell Death, Oxidative Stress, Mitochondrial Proteins, Caloric Restriction, Sirtuins, Mitochondrial Dynamics
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