Mitochondrial DNA deletion mutations and sarcopenia
Abstract
This manuscript summarizes our studies on mitochondrial DNA and enzymatic abnormalities that accumulate, with age, in skeletal muscle. Specific quadricep muscles, rectus femoris in the rat and vastus lateralis in the rhesus monkey, were used in these studies. These muscles exhibit considerable sarcopenia, the loss of muscle mass with age. The focal accumulation of mtDNA deletion mutations and enzymatic abnormalities in aged skeletal muscle necessitates a histologic approach in which every muscle fiber is examined for electron transport system (ETS) enzyme activity along its length. These studies demonstrate that ETS abnormalities accumulate to high levels within small regions of aged muscle fibers. Concomitant with the ETS abnormalities, we observe intrafiber atrophy and, in many cases, fiber breakage. Laser capture microdissection facilitates analysis of individual fibers from histologic sections and demonstrates a tight association between mtDNA deletion mutations and the ETS abnormalities. On the basis of these results, we propose a molecular basis for skeletal muscle fiber loss with age, a process beginning with the mtDNA deletion event and culminating with muscle fiber breakage and loss.
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The role of mitochondrial dysfunction in the etiology of sarcopenia has been extensively characterized.
“The role of mitochondrial dysfunction in the etiology of sarcopenia has been extensively characterized (17, 18, 19, 20).”
From Discovering pathways of sarcopenia in older adults: a role for insulin resistance on mitochondria dysfunction (2011) · cites this paper as [17]
Cites
MITOCHONDRIAL DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASES
Linnane, A. W., Ozawa, T., Marzuki, S., & Tanaka, M. (1989) · The Lancet · doi:10.1016/s0140-6736(89)92145-4 · Cited by 1,192 · see citing works
Detection of a specific mitochondrial DNA deletion in tissues of older humans
Cortopassi, G. A., & Arnheim, N. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.23.6927 · Cited by 785 · see citing works
WANAGAT, J., CAO, Z., PATHARE, P., & AIKEN, J. M. (2001) · The FASEB Journal · doi:10.1096/fj.00-0320com · Cited by 378 · see citing works
Self-citationMüller‐Höcker, J. (1990) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(90)90006-9 · Cited by 284 · see citing works
Free radical theory of aging: Consequences of mitochondrial aging
Harman, D. (1983) · AGE · doi:10.1007/bf02432509 · Cited by 244 · see citing works
Is Cell Aging Caused by Respiration-Dependent Injury to the Mitochondrial Genome?
Fleming, J. E., Miquel, J., Cottrell, S. F., Yengoyan, L. S., & Economos, A. C. (2009) · Gerontology · doi:10.1159/000212510 · Cited by 242 · see citing works
Multiple mitochondrial DNA deletions in an elderly human individual
Zhang, C., Baumer, A., Maxwell, R. J., Linnane, A. W., & Nagley, P. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)80321-7 · Cited by 214 · see citing works
Cao, Z. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.21.4502 · Cited by 170 · see citing works
Self-citationMüller-Höcker, J., Seibel, P., Schneiderbanger, K., & Kadenbach, B. (1993) · Virchows Archiv A Pathological Anatomy and Histopathology · doi:10.1007/bf01605127 · Cited by 168 · see citing works
Caloric restriction reduces fiber loss and mitochondrial abnormalities in aged rat muscle
Aspnes, L. E., Lee, C. M., Weindruch, R. H., Chung, S. S., Roecker, E. B., & Aiken, J. M. (1997) · The FASEB Journal · doi:10.1096/fasebj.11.7.9212081 · Cited by 163 · see citing works
Self-citationMultiple Deletions Are Detectable in Mitochondrial DNA of Aging Mice
Tanhauser, S. M., & Laipis, P. J. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.42.24769 · Cited by 160 · see citing works
High levels of mitochondrial DNA deletions in skeletal muscle of old rhesus monkeys
Schwarze, S. R., Lee, C. M., Chung, S. S., Roecker, E. B., Weindruch, R. H., & Aiken, J. M. (1995) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(95)01611-3 · Cited by 121 · see citing works
Self-citationAssociation of age-related mitochondrial abnormalities with skeletal muscle fiber atrophy
Lee, C. M., Lopez, M. E., Weindruch, R. H., & Aiken, J. M. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00185-3 · Cited by 121 · see citing works
Self-citationMultiple Mitochondrial DNA Deletions Associated With Age in Skeletal Muscle of Rhesus Monkeys
Lee, C. M., Chung, S. S., Kaczkowski, J. M., Weindruch, R. H., & Aiken, J. M. (1993) · Journal of Gerontology · doi:10.1093/geronj/48.6.b201 · Cited by 115 · see citing works
Self-citationCellular phenotypes of age-associated skeletal muscle mitochondrial abnormalities in rhesus monkeys
Lopez, M. E., Zeeland, N. L. V., Dahl, D. B., Weindruch, R. H., & Aiken, J. M. (2000) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(00)00059-2 · Cited by 74 · see citing works
Self-citationMultiple age-associated mitochondrial DNA deletions in skeletal muscle of mice
Chung, S. S., Weindruch, R. H., Schwarze, S. R., McKenzie, D. I., & Aiken, J. M. (1994) · Aging Clinical and Experimental Research · doi:10.1007/bf03324239 · Cited by 68 · see citing works
Self-citationMultiple Deletions in Mitochondrial DNA Are Present in Senescent Mouse Brain
Brossas, J., Barreau, E., Courtois, Y., & Tréton, J. (1994) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1994.1980 · Cited by 58 · see citing works
Multiple, large deletions in rat mitochondrial DNA: evidence for a major hot spot
Tuyle, G. C. V., Gudikote, J. P., Hurt, V. R., Miller, B. B., & Moore, C. A. (1996) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/0027-5107(95)00165-4 · Cited by 50 · see citing works
Lee, C. M., Eimon, P. M., Weindruch, R. H., & Aiken, J. M. (1994) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(94)90029-9 · Cited by 31 · see citing works
Self-citationTelomerase activity in human germline and embryonic tissues and cells
Wright, W. E., Piatyszek, M. A., Rainey, W. E., Byrd, W., & Shay, J. W. (1996) · Developmental Genetics · doi:10.1002/(sici)1520-6408(1996)18:2
Self-citation
Flagged first, then by citations
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Review Article: Sarcopenia: Causes, Consequences, and Preventions
Marcell, T. J. (2003) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/58.10.m911 · Cited by 536 · see citing works
Exercise Attenuates the Major Hallmarks of Aging
Garatachea, N., Pareja-Galeano, H., Sanchis-Gomar, F., Santos-Lozano, A., Fiuza-Luces, C., Morán, M., Emanuele, E., Joyner, M. J., & Lucia, A. (2015) · Rejuvenation Research · doi:10.1089/rej.2014.1623 · Cited by 413 · see citing works
Barrera, G., Pizzimenti, S., Daga, M., Dianzani, C., Arcaro, A., Cetrangolo, G. P., Giordano, G., Cucci, M. A., Graf, M. E., & Gentile, F. (2018) · Antioxidants · doi:10.3390/antiox7080102 · Cited by 338 · see citing works
Picard, M., Ritchie, D., Wright, K. J., Romestaing, C., Thomas, M. M., Rowan, S. L., Taivassalo, T., & Hepple, R. T. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00628.x · Cited by 238 · see citing works
Mechanisms of skeletal muscle aging: insights from <i>Drosophila</i> and mammalian models
Demontis, F., Piccirillo, R., Goldberg, A. L., & Perrimon, N. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.012559 · Cited by 238 · see citing works
Skeletal muscle aging and the mitochondrion
Johnson, M. L., Robinson, M. M., & Nair, K. S. (2013) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2012.12.003 · Cited by 233 · see citing works
Bunout, D. C., Barrera, G., Leiva, L., Vivien Gattas, Z., de la Maza, M. P., Avendaño, M., & Hirsch, S. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.05.001 · Cited by 231 · see citing works
Aberrant mitochondrial homeostasis in the skeletal muscle of sedentary older adults
Safdar, A., Hamadeh, M. J., Kaczor, J. J., Raha, S., deBeer, J., & Tarnopolsky, M. A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010778 · Cited by 217 · see citing works
Apoptosis in muscle atrophy: Relevance to sarcopenia
Dupont‐Versteegden, E. E. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.04.003 · Cited by 207 · see citing works
Modulation of reactive oxygen species in skeletal muscle by myostatin is mediated through NF-κB
Sriram, S., Subramanian, S., Sathiakumar, D., Venkatesh, R., Salerno, M. S., McFarlane, C. D., Kambadur, R., & Sharma, M. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00734.x · Cited by 189 · see citing works
Dysfunctional Nrf2–Keap1 redox signaling in skeletal muscle of the sedentary old
Safdar, A., DeBeer, J., & Tarnopolsky, M. A. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.08.010 · Cited by 158 · see citing works
Mitochondria initiate and regulate sarcopenia
Alway, S. E., Mohamed, J. S., & Myers, M. J. (2017) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000101 · Cited by 153 · see citing works
“Indeed, increased mtDNA mutations have been found in fiber regions that contain oxidative damage (2,90).”
BackgroundOxidative damage and age-related functional declines
Martin, I., & Grotewiel, M. S. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.008 · Cited by 152 · see citing works
Hütter, E., Skovbro, M., Lener, B., Prats, C., Rabøl, R., Dela, F., & Jansen‐Dürr, P. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00282.x · Cited by 149 · see citing works
The role of mitochondria in neurodegenerative diseases
Filosto, M., Scarpelli, M., Cotelli, M. S., Vielmi, V., Todeschini, A., Gregorelli, V., Tonin, P., Tomelleri, G., & Padovani, A. (2011) · Journal of Neurology · doi:10.1007/s00415-011-6104-z · Cited by 140 · see citing works
Abbatecola, A. M., Paolisso, G., Fattoretti, P., Evans, W. J., Fiore, V., Dicioccio, L., & Lattanzio, F. (2011) · The Journal of nutrition, health and aging · doi:10.1007/s12603-011-0366-0 · Cited by 137 · see citing works
Exercise and nutritional interventions for improving aging muscle health
Forbes, S. C., Little, J. P., & Candow, D. G. (2012) · Endocrine · doi:10.1007/s12020-012-9676-1 · Cited by 133 · see citing works
Mitochondrial abnormalities in inclusion-body myositis
Oldfors, A., Moslemi, A. ‐., Jonasson, L., Ohlsson, M., Kollberg, G., & Lindberg, C. (2006) · Neurology · doi:10.1212/01.wnl.0000192127.63013.8d · Cited by 135 · see citing works
Energetics of Walking in Elderly People: Factors Related to Gait Speed
Fiser, W., Hays, N. P., Rogers, S. C., Kajkenova, O., Williams, A. E., Evans, C. M., & Evans, W. J. (2010) · The Journals of Gerontology Series A · doi:10.1093/gerona/glq137 · Cited by 130 · see citing works
Aryaman, J., Johnston, I. G., & Jones, N. S. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00718 · Cited by 121 · see citing works
Aging as a catabolic malfunction
Terman, A., & Brunk, U. T. (2004) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2004.03.009 · Cited by 114 · see citing works
Myocyte aging and mitochondrial turnover
Terman, A., & Brunk, U. T. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.01.005 · Cited by 100 · see citing works
The physiological roles of Sirt1 in skeletal muscle
Pardo, P. S., & Boriek, A. M. (2011) · Aging · doi:10.18632/aging.100312 · Cited by 99 · see citing works
Mitochondrial Impairment in Sarcopenia
Bellanti, F., Buglio, A. L., & Vendemiale, G. (2021) · Biology · doi:10.3390/biology10010031 · Cited by 99 · see citing works
Mitochondria and Aging—The Role of Exercise as a Countermeasure
Nilsson, M. I., & Tarnopolsky, M. A. (2019) · Biology · doi:10.3390/biology8020040 · Cited by 92 · see citing works
Baker, D. J., Betik, A. C., Krause, D. J., & Hepple, R. T. (2006) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/61.7.675 · Cited by 89 · see citing works
Age-Related Changes in Speed and Mechanism of Adult Skeletal Muscle Stem Cell Migration
Collins‐Hooper, H., Woolley, T. E., Dyson, L., Patel, A. P., Potter, P. K., Baker, R. E., Gaffney, E. A., Maini, P. K., Dash, P. R., & Patel, K. (2012) · Stem Cells · doi:10.1002/stem.1088 · Cited by 82 · see citing works
The aging myocardium: roles of mitochondrial damage and lysosomal degradation
Terman, A., & Brunk, U. T. (2005) · Heart, Lung and Circulation · doi:10.1016/j.hlc.2004.12.023 · Cited by 80 · see citing works
Cobley, J. N., Moult, P. R., Burniston, J. G., Morton, J. P., & Close, G. L. (2014) · Biogerontology · doi:10.1007/s10522-014-9546-8 · Cited by 69 · see citing works
Regulatory circuitry of TWEAK‐Fn14 system and PGC‐1α in skeletal muscle atrophy program
Hindi, S. M., Mishra, V. K., Bhatnagar, S., Tajrishi, M. M., Ogura, Y., Yan, Z., Burkly, L. C., Zheng, T. S., & Kumar, A. (2013) · The FASEB Journal · doi:10.1096/fj.13-242123 · Cited by 68 · see citing works
The impact of age-related dysregulation of the angiotensin system on mitochondrial redox balance
Vajapey, R. S., Rini, D. A., Walston, J. D., & Abadir, P. M. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00439 · Cited by 69 · see citing works
Huang, J. H., & Hood, D. A. (2009) · IUBMB Life · doi:10.1002/iub.164 · Cited by 66 · see citing works
Tarnopolsky, M. A. (2009) · Applied Physiology Nutrition and Metabolism · doi:10.1139/h09-022 · Cited by 59 · see citing works
Ageing of skeletal muscle extracellular matrix and mitochondria: finding a potential link
Cai, L., Shi, L., Peng, Z., Sun, Y., & Chen, J. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2240707 · Cited by 60 · see citing works
McKiernan, S. H., Colman, R. J., Aiken, E. J., Evans, T. D., Beasley, T. M., Aiken, J. M., Weindruch, R. H., & Anderson, R. M. (2011) · Experimental Gerontology · doi:10.1016/j.exger.2011.12.009 · Cited by 53 · see citing works
Self-citationMitochondrial and skeletal muscle health with advancing age
Konopka, A. R., & Nair, K. S. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.05.008 · Cited by 54 · see citing works
The effect of calorie restriction on mouse skeletal muscle is sex, strain and time-dependent
Boldrin, L., Ross, J. A., Whitmore, C. L., Doreste, B., Beaver, C., Eddaoudi, A., Pearce, D. J., & Morgan, J. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-04896-y · Cited by 51 · see citing works
The Role of Lonp1 on Mitochondrial Functions during Cardiovascular and Muscular Diseases
Zanini, G., Selleri, V., Malerba, M., Solodka, K., Sinigaglia, G., Nasi, M., Mattioli, A. V., & Pinti, M. (2023) · Antioxidants · doi:10.3390/antiox12030598 · Cited by 49 · see citing works
Tarnopolsky, M. A., & Safdar, A. (2008) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h07-142 · Cited by 47 · see citing works
Skeletal muscle as an experimental model of choice to study tissue aging and rejuvenation
Etienne, J., Liu, C., Skinner, C. M., Conboy, M. J., & Conboy, I. M. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-0222-1 · Cited by 48 · see citing works
Respiratory chain deficiency in aged spinal motor neurons
Rygiel, K. A., Grady, J. P., & Turnbull, D. M. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.02.027 · Cited by 41 · see citing works
Longitudinal analysis of early stage sarcopenia in aging rhesus monkeys
McKiernan, S. H., Colman, R. J., Lopez, M. E., Beasley, T. M., Weindruch, R. H., & Aiken, J. M. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.09.014 · Cited by 37 · see citing works
Self-citationInjury and adaptive mechanisms in skeletal muscle
Cutlip, R. G., Baker, B. A., Hollander, M. S., & Ensey, J. S. (2008) · Journal of Electromyography and Kinesiology · doi:10.1016/j.jelekin.2008.06.007 · Cited by 36 · see citing works
Huang, J. H., Joseph, A.-M., Ljubicic, V., Iqbal, S., & Hood, D. A. (2010) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glp201 · Cited by 35 · see citing works
von Wurmb‐Schwark, N., Cavelier, L. B., & Cortopassi, G. A. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.12.003 · Cited by 29 · see citing works
Jeong, I., Cho, E., Yook, J.-S., Choi, Y., Park, D., Kang, J., Lee, S.-H., Seo, D. Y., Jung, S., & Kwak, H. (2024) · Life · doi:10.3390/life14080962 · Cited by 33 · see citing works
Kimoloi, S., Sen, A., Günther, S., Braun, T. W., Bruegmann, T., Sasse, P., Wiesner, R. J., Pla‐Martín, D., & Baris, O. R. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13026 · Cited by 29 · see citing works
Ginkgo biloba Extract EGb 761 and Wisconsin Ginseng Delay Sarcopenia in Caenorhabditis elegans
Cao, Z., Wu, Y., Curry, K., Wu, Z., Christen, Y., & Luo, Y. (2007) · The Journals of Gerontology Series A · doi:10.1093/gerona/62.12.1337 · Cited by 29 · see citing works
Self-citationDirect Sampling from Muscle Cross Sections for Electrophoretic Analysis of Individual Mitochondria
Ahmadzadeh, H., Johnson, R. D., Thompson, L. V., & Arriaga, E. A. (2003) · Analytical Chemistry · doi:10.1021/ac034809g · Cited by 28 · see citing works
Hou, Y., Xie, Z., Zhao, X., Yuan, Y., Dou, P., & Wang, Z. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219628 · Cited by 27 · see citing works
American Ginseng Supplementation Induces an Oxidative Stress in Postmenopausal Women
Dickman, J. R., Koenig, R. T., & Ji, L. L. (2009) · Journal of the American College of Nutrition · doi:10.1080/07315724.2009.10719773 · Cited by 26 · see citing works
Guescini, M., Fatone, C., Stocchi, L., Guidi, C., Potenza, L., Ditroilo, M., Ranchelli, A., Loreto, C. D., Sisti, D., Feo, P. D., et al. (2007) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2007.01.012 · Cited by 25 · see citing works
Bellanti, F., Buglio, A. L., & Vendemiale, G. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14122588 · Cited by 24 · see citing works
Wanagat, J., Ahmadieh, N., Bielas, J. H., Ericson, N. G., & Remmen, H. V. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.11.012 · Cited by 22 · see citing works
Self-citationHerbst, A. J., Johnson, C. J., Hynes, K., McKenzie, D. I., & Aiken, J. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059006 · Cited by 21 · see citing works
Self-citationCosta, E. L., Filho, P. S. D. C. B., Moura, M. D. S., de Sousa, T. S., Lemos, A., & Pedrosa, M. A. C. (2012) · Arquivos Brasileiros de Endocrinologia & Metabologia · doi:10.1590/s0004-27302012000500006 · Cited by 13 · see citing works
Metabolic and Molecular Aspects of Sarcopenia
Cade, W. T., & Yarasheski, K. E. (2007) · Humana Press eBooks · doi:10.1007/978-1-59259-963-9_50 · Cited by 12 · see citing works
Li, Y.-F., Li, H.-Z., Hu, P., Deng, J., Banoei, M. M., Sharma, L. K., & Bai, Y. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp1162 · Cited by 11 · see citing works
Skrzep-Poloczek, B., Poloczek, J., Chełmecka, E., Kazura, W., Dulska, A., Idzik, M., Jochem, J., & Stygar, D. M. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4598437 · Cited by 11 · see citing works
Sarcopenia: characteristics, genesis, remedies
Tano, G. D., Fulle, S., Pietrangelo, T., Bellomo, R. G., & Fanò, G. (2005) · Sport Sciences for Health · doi:10.1007/s11332-2005-004-0013-4 · Cited by 10 · see citing works
Musci, R. V., Fuqua, J. D., Peelor, F. F., Nguyen, H. V. M., Richardson, A. G., Choi, S., Miller, B. F., & Wanagat, J. (2024) · GeroScience · doi:10.1007/s11357-024-01344-4 · Cited by 5 · see citing works
Self-citationEstudo histomorfométrico do músculo esquelético de ratos em anestro
Moreira, M. D. A., Brito, M. V. H., Brito, N. M. B., & Filho, M. D. S. L. F. (2005) · Acta Cirúrgica Brasileira · doi:10.1590/s0102-86502005000400012 · Cited by 5 · see citing works
Multi-Omics Approach to Mitochondrial DNA Damage in Human Muscle Fibers
Elstner, M., Olszewski, K., Prokisch, H., Klopstock, T., & Murgia, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011080 · Cited by 5 · see citing works
Idzik, M., Poloczek, J., Skrzep-Poloczek, B., Chełmecka, E., Jochem, J., & Stygar, D. M. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1358858 · Cited by 5 · see citing works
Ablation of Ghrelin Receptor Mitigates the Metabolic Decline of Aging Skeletal Muscle
O’Reilly, C. L., Lin, L., Wang, H., Fluckey, J. D., & Sun, Y. (2022) · Genes · doi:10.3390/genes13081368 · 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
Oflazer, P. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)86018-0 · Cited by 4 · see citing works
Molecular Regulation and Rejuvenation of Muscle Stem (Satellite) Cell Aging
Meiliana, A., Dewi, N. M., & Wijaya, A. (2015) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v7i2.73 · Cited by 4 · see citing works
Aging and Lysosomal Degradation of Cellular Constituents
Terman, A., & Brunk, U. T. (2003) · Springer eBooks · doi:10.1007/978-94-017-0667-4_15 · Cited by 3 · see citing works
Association between protoporphyrin IX and sarcopenia: a cross sectional study
Kao, C.-C., Yang, Z., & Chen, W. (2021) · BMC Geriatrics · doi:10.1186/s12877-021-02331-6 · Cited by 3 · see citing works
Lakshmanan, L. N., Yee, Z., Gruber, J., Halliwell, B. B., & Gunawan, R. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/254631 · Cited by 3 · see citing works
Antioxidant Supplementation in Older Persons
Cesari, M., Cerullo, F., Demougeot, L., Zamboni, V., Gambassi, G., & Vellas, B. J. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_175 · Cited by 2 · see citing works
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Bennett, R. M. (2004) · Journal of Musculoskeletal Pain · doi:10.1300/j094v12n03_01 · Cited by 2 · see citing works
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Alway, S. E. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822146-4.00004-1 · Cited by 1 · see citing works
Wolkow, C. (2010) · Interdisciplinary topics in gerontology · doi:10.1159/000319996 · Cited by 1 · see citing works
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Smith, B. A. (2014) · Scholarship@Western (Western University)
Role of Myostatin in oxidative stress in skeletal muscle
Sandhya, S. (2013) · doi:10.32657/10356/53725
Costa, E. L., Moura, M. D. S., de Sousa, T. S., Lemos, A., Alessandra, M., & Pedrosa, C. (2012)
Thermodynamic analysis of DNA hybridization signatures near mitochondrial DNA deletion breakpoints
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Anti-Aging Medicine LiteratureWatch
(2002) · Rejuvenation Research · doi:10.1089/109454502321091509
Additional file 1 of Association between protoporphyrin IX and sarcopenia: a cross sectional study
Kao, C.-C., Yang, Z.-Y., & Chen, W.-L. (2021) · Figshare · doi:10.6084/m9.figshare.14853591
Martin, I. (2008) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/pgcp-c821
- Authors
- AIKEN, J., BUA, E., CAO, Z., LOPEZ, M., WANAGAT, J., McKENZIE, D., & McKIERNAN, S.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- AIKEN, JUDD
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 2002-04
- Volume
- 959
- Issue
- 1
- Pages
- 412-423
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W2052008941
- Cited by
- 85
- References
- 21
- Citations by year
- 2024: 2 · 2023: 2 · 2022: 4 · 2021: 6 · 2020: 2 · 2019: 3 · 2018: 3 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 7 · 2013: 6 · 2012: 4
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (AG17543, R01AG017543, R01AG011604, P01AG011915, T32AG000213)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
- Keywords
- sarcopenia, skeletal muscle aging, muscle fiber atrophy, laser capture microdissection, rectus femoris, vastus lateralis
- MeSH terms
- Aging, Animals, Electron Transport Complex IV, DNA, Mitochondrial, Mutation, Statistics as Topic, Succinate Dehydrogenase, Muscle, Skeletal, Microscopy, Confocal, Mitochondrial Diseases
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