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Denervation-induced skeletal muscle atrophy is associated with increased mitochondrial ROS production
Abstract
Reactive oxygen species (ROS), especially mitochondrial ROS, are postulated to play a significant role in muscle atrophy. We report a dramatic increase in mitochondrial ROS generation in three conditions associated with muscle atrophy: in aging, in mice lacking CuZn-SOD (Sod1(-/-)), and in the neurodegenerative disease, amyotrophic lateral sclerosis (ALS). ROS generation in muscle mitochondria is nearly threefold higher in 28- to 32-mo-old than in 10-mo-old mice and is associated with a 30% loss in gastrocnemius mass. In Sod1(-/-) mice, muscle mitochondrial ROS production is increased >100% in 20-mo compared with 5-mo-old mice along with a >50% loss in muscle mass. ALS G93A mutant mice show a 75% loss of muscle mass during disease progression and up to 12-fold higher muscle mitochondrial ROS generation. In a second ALS mutant model, H46RH48Q mice, ROS production is approximately fourfold higher than in control mice and is associated with a less dramatic loss (30%) in muscle mass. Thus ROS production is strongly correlated with the extent of muscle atrophy in these models. Because each of the models of muscle atrophy studied are associated to some degree with a loss of innervation, we were interested in determining whether denervation plays a role in ROS generation in muscle mitochondria isolated from hindlimb muscle following surgical sciatic nerve transection. Seven days post-denervation, muscle mitochondrial ROS production increased nearly 30-fold. We conclude that enhanced generation of mitochondrial ROS may be a common factor in the mechanism underlying denervation-induced atrophy.
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“Enhanced generation of mitochondrial ROS may be a common factor in the mechanism underlying denervation-induced atrophy [15].”
From Nutraceuticals in the Prevention and Treatment of the Muscle Atrophy (2021) · cites this paper as [15]
Citations
Cites
Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation
Gurney, M. E., Pu, H., Chiu, A. Y., Dal Canto, M. C., Polchow, C. Y., Alexander, D. D., Caliendo, J., Hentati, A., Kwon, Y. W., Deng, H.-X., et al. (1994) · Science · doi:10.1126/science.8209258 · Cited by 4,143
Reactivity of HO2/O− 2 radicals in aqueous solution
Bielski, B. H. J., Cabelli, D. E., Arudi, R. L., & Ross, A. B. (1985) · Journal of Physical and Chemical Reference Data · doi:10.1063/1.555739 · Cited by 2,169
The Respiratory Chain and Oxidative Phosphorylation
Chance, B., & Williams, G. R. (1956) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9780470122624.ch2 · Cited by 2,084
[7] Mitochondrial respiratory control and the polarographic measurement of ADP : O ratios
Estabrook, R. W. (1967) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(67)10010-4 · Cited by 1,781
Production of Reactive Oxygen Species by Mitochondria
Chen, Q., Vazquez, E. J., Moghaddas, S., Hoppel, C. L., & Lesnefsky, E. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304854200 · Cited by 1,616
Zhou, M., Diwu, Z. J., Panchuk-Voloshina, N., & Haugland, R. P. (1997) · Analytical Biochemistry · doi:10.1006/abio.1997.2391 · Cited by 1,400
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
Fischer, L. R., Culver, D. G., Tennant, P., Davis, A. A., Wang, M.-S., Castellano-Sanchez, A. A., Khan, J., Polak, M. A., & Glass, J. D. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2003.10.004 · Cited by 1,383
IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice
Cai, D., Frantz, J. D., Tawa, N. E., Melendez, P. A., Oh, B.-C., Lidov, H. G. W., Hasselgren, P.-O., Frontera, W. R., Lee, J., Glass, D. J., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.027 · Cited by 1,367
Partial Resolution of the Enzymes Catalyzing Oxidative Phosphorylation
Kagawa, Y., & Racker, E. (1971) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)61930-1 · Cited by 1,361
Mitochondrial metabolism of reactive oxygen species
Andreyev, A. Y., Kushnareva, Y. E., & Starkov, A. A. (2005) · Biochemistry (Moscow) · doi:10.1007/s10541-005-0102-7 · Cited by 1,336
Reaume, A. G., Elliott, J. L., Hoffman, E. K., Kowall, N. W., Ferrante, R. J., Siwek, D. F., Wilcox, H. M., Flood, D. G., Beal, M. F., Brown, R. H., et al. (1996) · Nature Genetics · doi:10.1038/ng0596-43 · Cited by 1,285
The Molecular Basis of Skeletal Muscle Atrophy
Jackman, R. W., & Kandarian, S. C. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00579.2003 · Cited by 1,008 · cited 2×
“How might the increase in mitochondrial ROS production contribute to the loss of muscle mass? Growing evidence implicates oxidative stress as an important regulator of pathways leading to muscle atrophy (27, 36, 65).”
BackgroundThe central executioners of apoptosis: caspases or mitochondria?
Green, D. R., & Kroemer, G. (1998) · Trends in Cell Biology · doi:10.1016/s0962-8924(98)01273-2 · Cited by 761
Mitochondria in homeostasis of reactive oxygen species in cell, tissues, and organism
Ježek, P., & Plecitá‐Hlavatá, L. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.05.013 · Cited by 753
Roubenoff, R., & HUGHES, V. A. (2000) · The Journals of Gerontology Series A · doi:10.1093/gerona/55.12.m716 · Cited by 698
Frey, D., Schneider, C., Xu, L., Borg, J., Spooren, W. P. J. M., & Caroni, P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02534.2000 · Cited by 683
Elchuri, S., Oberley, T. D., Qi, W., Eisenstein, R. S., Jackson Roberts, L., Van Remmen, H., Epstein, C. J., & Huang, T.-T. (2005) · Oncogene · doi:10.1038/sj.onc.1208207 · Cited by 667
Li, Y.-P., Chen, Y., John, J., Moylan, J. S., Jin, B., Mann, D. L., & Reid, M. B. (2005) · The FASEB Journal · doi:10.1096/fj.04-2364com · Cited by 634
Atrophy of the soleus muscle by hindlimb unweighting
Thomason, D. B., & Booth, F. W. (1990) · Journal of Applied Physiology · doi:10.1152/jappl.1990.68.1.1 · Cited by 631
The numbers of limb motor neurons in the human lumbosacral cord throughout life
Tomlinson, B. E., & Irving, D. (1977) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(77)90069-7 · Cited by 602
ΔΨ m ‐Dependent and ‐independent production of reactive oxygen species by rat brain mitochondria
Votyakova, T. V., & Reynolds, I. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00548.x · Cited by 601
Dupuis, L., Oudart, H., René, F., de Aguilar, J. G., & Loeffler, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402026101 · Cited by 532
Skeletal muscle weakness in old age
Brooks, S. V., & Faulkner, J. A. (1994) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199404000-00006 · Cited by 511
Müller, F. L., Song, W., Liu, Y., Chaudhuri, A. R., Pieke-Dahl, S., Strong, R., Huang, T., Epstein, C. J., Roberts, L. J., CSETE, M. E., et al. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.01.036 · Cited by 466
Skeletal muscle weakness in old age: underlying mechanisms.
Brooks, S. V., & Faulkner, J. A. (1994) · PubMed · Cited by 463
Williams, M. D., Remmen, H. V., Conrad, C. C., Huang, T., Epstein, C. J., & Richardson, A. G. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.43.28510 · Cited by 453
The contribution of reactive oxygen species to sarcopenia and muscle ageing
Fulle, S., Protasi, F., Tano, G. D., Pietrangelo, T., Beltramin, A., Boncompagni, S., Vecchiet, L., & Fanò, G. (2003) · Experimental Gerontology · doi:10.1016/j.exger.2003.09.012 · Cited by 451
Dependence of H2O2 formation by rat heart mitochondria on substrate availability and donor age
Hansford, R. G., Hogue, B. A., & Mildaziene, V. (1997) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1022420007908 · Cited by 447 · cited 10×
“32) and in the absence of respiratory inhibitors (32, 80).”
BackgroundResultInfluentialA Simple and Rapid Assay of Oxidative Phosphorylation
Chance, B., & Williams, G. R. (1955) · Nature · doi:10.1038/1751120a0 · Cited by 412
Intracellular signaling during skeletal muscle atrophy
Kandarian, S. C., & Jackman, R. W. (2005) · Muscle & Nerve · doi:10.1002/mus.20442 · Cited by 405
Gould, T. W., Buss, R. R., Vinsant, S. L., Prevette, D. M., Sun, W., Knudson, C. M., Milligan, C., & Oppenheim, R. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2315-06.2006 · Cited by 397
Mechanisms of disuse muscle atrophy: role of oxidative stress
Powers, S. K., Kavazis, A. N., & DeRuisseau, K. C. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00469.2004 · Cited by 368
Spinal Muscular Atrophy: A Deficiency in a Ubiquitous Protein; a Motor Neuron-Specific Disease
Monani, U. R. (2005) · Neuron · doi:10.1016/j.neuron.2005.12.001 · Cited by 352
NFκB and AP-1 mediate transcriptional responses to oxidative stress in skeletal muscle cells
Zhou, L. Z.-H., Johnson, A. P., & Rando, T. A. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00719-5 · Cited by 323
Spherical reflector as an electromagnetic-missile launcher
Shen, H.-M. (1990) · Journal of Applied Physics · doi:10.1063/1.347115 · Cited by 307
Biochemical and Osmotic Properties of Skeletal Muscle Mitochondria
Chappell, J., & PERRY, S. V. (1954) · Nature · doi:10.1038/1731094a0 · Cited by 291
Sarcopenia of Aging and Its Metabolic Impact
Karakelides, H., & Nair, K. S. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)68005-2 · Cited by 271
Neural control of aging skeletal muscle
Delbono, O. (2003) · Aging Cell · doi:10.1046/j.1474-9728.2003.00011.x · Cited by 248
Effect of denervation on mitochondrially mediated apoptosis in skeletal muscle.
Adhihetty, P. J., O'Leary, M. F. N., Chabi, B., Wicks, K. L., & Hood, D. A. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00768.2006 · Cited by 240
Wang, J., Xu, G. M., Gonzales, V., Coonfield, M. L., Fromholt, D., Copeland, N. G., Jenkins, N. A., & Borchelt, D. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0498 · Cited by 235
Skeletal muscle atrophy in old rats: Differential changes in the three fiber types
Holloszy, J. O., Chen, M. W., Cartee, G. D., & Young, J. C. (1991) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(91)90131-i · Cited by 230
Mansouri, A., Muller, F. L., Liu, Y., Ng, R., Faulkner, J., Hamilton, M., Richardson, A., Huang, T.-T., Epstein, C. J., & Van Remmen, H. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.11.004 · Cited by 227
Mitochondria-associated apoptotic signalling in denervated rat skeletal muscle
Siu, P. M., & Alway, S. E. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.081083 · Cited by 216
Skeletal muscle gene expression in space-flown rats
Nikawa, T., Ishidoh, K., Hirasaka, K., Ishihara, I., Ikemoto, M., Kano, M., Kominami, E., Nonaka, I., Ogawa, T., Adams, G. R., et al. (2004) · The FASEB Journal · doi:10.1096/fj.03-0419fje · Cited by 212
Joza, N. A., Oudit, G. Y., Brown, D., Bénit, P., Kassiri, Z., Vahsen, N., Benoît, L. A., Patel, M. M., Nowikovsky, K., Vassault, A. J., et al. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.23.10261-10272.2005 · Cited by 206
Partial Resolution of the Enzymes Catalyzing Oxidative Phosphorylation
Hinkle, P. C., Butow, R. A., Racker, E., & Chance, B. (1967) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99410-x · Cited by 195
The use of transgenic mouse models of amyotrophic lateral sclerosis in preclinical drug studies
Gurney, M. E. (1997) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(97)00247-5 · Cited by 189
Molecular determinants of skeletal muscle mass: getting the “AKT” together
Nader, G. A. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.02.026 · Cited by 184
Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy
Shefner, J. M., Reaume, A. G., Flood, D. G., Scott, R. W., Kowall, N. W., Ferrante, R. J., Siwek, D. F., Upton-Rice, M. N., & Brown, R. H. (1999) · Neurology · doi:10.1212/wnl.53.6.1239 · Cited by 184
Scheffler, I. E. (1999) · Wiley eBooks · doi:10.1002/0471223891 · Cited by 181
Cancer cachexia: Metabolic alterations and clinical manifestations
Tisdale, M. J. (1997) · Nutrition · doi:10.1016/s0899-9007(96)00313-9 · Cited by 172
Superoxide-Mediated Cytotoxicity in Superoxide Dismutase-Deficient Fetal Fibroblasts
Huang, T., Yasunami, M., Carlson, E. J., Gillespie, A. M., Reaume, A. G., Hoffman, E. K., Chan, P. H., Scott, R. W., & Epstein, C. J. (1997) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0237 · Cited by 169
Properties of single motor units in medial gastrocnemius muscles of adult and old rats.
Kadhiresan, V. A., Hassett, C., & Faulkner, J. A. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021402 · Cited by 155
Cino, M., & Maestro, R. F. D. (1989) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(89)90148-3 · Cited by 151
Role of Apoptosis in Sarcopenia
Leeuwenburgh, C. (2003) · The Journals of Gerontology Series A · doi:10.1093/gerona/58.11.m999 · Cited by 147
Dupuis, L., Scala, F. D., René, F., de Tapia, M., Oudart, H., Pradat, P., Meininger, V., & Loeffler, J. (2003) · The FASEB Journal · doi:10.1096/fj.02-1182fje · Cited by 134
Knyushko, T. V., Sharov, V. S., Williams, T. D., Schöneich, C., & Bigelow, D. J. (2005) · Biochemistry · doi:10.1021/bi051226n · Cited by 131
Krishnamoorthy, G., & Hinkle, P. C. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)77873-9 · Cited by 129
DENERVATION CHANGES IN MAMMALIAN STRIATED MUSCLE
Sunderland, S., & Ray, L. J. (1950) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.13.3.159 · Cited by 127
Supplementation of Vitamin E May Attenuate Skeletal Muscle Immobilization Atrophy
Duarte, J. A., & Soares, J. M. C. (1997) · International Journal of Sports Medicine · doi:10.1055/s-2007-972612 · Cited by 122
Apoptosis and muscle fibre loss in neuromuscular disorders
Tews, D. S. (2002) · Neuromuscular Disorders · doi:10.1016/s0960-8966(02)00030-5 · Cited by 113
Mitochondrial adaptations in denervated muscle: relationship to muscle performance
Wicks, K. L., & Hood, D. A. (1991) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1991.260.4.c841 · Cited by 111
[14] Skeletal muscle mitochondria
Ernster, L., & Nordenbrand, K. (1967) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(67)10017-7 · Cited by 109
Hindlimb Motor Neurons Require Cu/Zn Superoxide Dismutase for Maintenance of Neuromuscular Junctions
Flood, D. G., Reaume, A. G., Gruner, J. A., Hoffman, E. K., Hirsch, J. D., Lin, Y., Dorfman, K. S., & Scott, R. W. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65162-0 · Cited by 104
Trace element movement and oxidative stress in skeletal muscle atrophied by immobilization
Kondo, H., Miura, M., Nakagaki, I., Sasaki, S., & Itokawa, Y. (1992) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1992.262.5.e583 · Cited by 102
Cardasis, C. A., & LaFontaine, D. (1987) · Muscle & Nerve · doi:10.1002/mus.880100303 · Cited by 85
Pak, J. W., Herbst, A. J., Bua, E. A., Gokey, N. G., McKenzie, D. I., & Aiken, J. M. (2003) · Aging Cell · doi:10.1046/j.1474-9728.2003.00034.x · Cited by 83
The Physiological Consequences of Bed Rest and Inactivity
Krasnoff, J. B., & Painter, P. (1999) · Advances in Renal Replacement Therapy · doi:10.1016/s1073-4449(99)70030-0 · Cited by 80
Oxidative stress and antioxidant enzyme upregulation in SOD1‐G93A mouse skeletal muscle
Mahoney, D. J., Kaczor, J. J., Bourgeois, J. M., Yasuda, N., & Tarnopolsky, M. A. (2006) · Muscle & Nerve · doi:10.1002/mus.20542 · Cited by 80
Kostrominova, T. Y., Dow, D. E., Dennis, R. G., Miller, R. A., & Faulkner, J. A. (2005) · Physiological Genomics · doi:10.1152/physiolgenomics.00210.2004 · Cited by 76
Raffaello, A., Laveder, P., Romualdi, C., Bean, C., Toniolo, L., Germinario, E., Megighian, A., Danieli‐Betto, D., Reggiani, C., & Lanfranchi, G. (2005) · Physiological Genomics · doi:10.1152/physiolgenomics.00051.2005 · Cited by 75
Fatigue of muscles weakened by death of motoneurons
Thomas, C. K., & Zijdewind, I. (2005) · Muscle & Nerve · doi:10.1002/mus.20400 · Cited by 73
Csukly, K., Ascah, A., Matas, J., Gardiner, P. F., Fontaine, E. M., & Burelle, Y. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.109702 · Cited by 68
New developments in diabetic neuropathy
Sullivan, K. A., & Feldman, E. L. (2005) · Current Opinion in Neurology · doi:10.1097/01.wco.0000178825.56414.52 · Cited by 67
Axonal sprouting at the neuromuscular junction of adult and aged rats
Fagg, G. E., Scheff, S. W., & Cotman, C. W. (1981) · Experimental Neurology · doi:10.1016/0014-4886(81)90257-0 · Cited by 61
Chemiosmotic energy transduction
Nicholls, D. G., & Ferguson, S. J. (2003) · Elsevier eBooks · doi:10.1016/b978-012518121-1/50003-8 · Cited by 59
Regulation of myogenin protein expression in denervated muscles from young and old rats
Kostrominova, T. Y., Macpherson, P. C. D., Carlson, B. M., & Goldman, D. J. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.1.r179 · Cited by 56
Arisato, T., Okubo, R., Arata, H., Abe, K., Fukada, K., Sakoda, S., Shimizu, A., Qin, X. H., Izumo, S., Osame, M., et al. (2003) · Acta Neuropathologica · doi:10.1007/s00401-003-0763-5 · Cited by 49
Blood flow, mitochondria, and performance in skeletal muscle after denervation and reinnervation
Eisenberg, H. A., & Hood, D. A. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.76.2.859 · Cited by 48
Muscle fatigue in old animals. Unique aspects of fatigue in elderly humans.
Faulkner, J. A., & Brooks, S. V. (1995) · PubMed · Cited by 41
Faulkner, J. A., & Brooks, S. V. (1995) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-1016-5_36 · Cited by 40
Kettle, A. J., Carr, A. C., & Winterbourn, C. C. (1994) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)90111-2 · Cited by 39
Joffe, M., Savage, N., & Isaacs, H. (1981) · Biochemical Journal · doi:10.1042/bj1960663 · Cited by 36
Treating respiratory failure in ALS: the details are becoming clearer
Oppenheimer, E. A. (2003) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(03)00035-2 · Cited by 28
A Novel Approach for Screening the Proteome for Changes in Protein Conformation
Pierce, A. P., deWaal, E., Remmen, H. V., Richardson, A. G., & Chaudhuri, A. R. (2006) · Biochemistry · doi:10.1021/bi052031i · Cited by 28
Biochemical functioning of mitochondria in normal and denervated mammalian skeletal muscle
Joffe, M., Savage, N., & Isaacs, H. (1981) · Muscle & Nerve · doi:10.1002/mus.880040608 · Cited by 20
Lebherz, H. G. (1984) · International Journal of Biochemistry · doi:10.1016/0020-711x(84)90217-9 · Cited by 11
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Metadata
- Authors
- Muller, F. L., Song, W., Jang, Y. C., Liu, Y., Sabia, M., Richardson, A., & Van Remmen, H.
- Affiliations
- Seoul National University (KR)
- The University of Texas at San Antonio Health Science Center (US)
- Venue
- American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
- Publisher
- American Physiological Society
- Published
- 2007-09
- Volume
- 293
- Issue
- 3
- Pages
- R1159-R1168
- ISSN
- 0363-6119 (ISSN-L)
- 1522-1490
- OpenAlex
- W2137182040
- Cited by
- 355
- References
- 88
- Citations by year
- 2026: 11 · 2025: 14 · 2024: 16 · 2023: 14 · 2022: 35 · 2021: 23 · 2020: 29 · 2019: 23 · 2018: 25 · 2017: 19 · 2016: 26 · 2015: 18 · 2014: 13 · 2013: 20 · 2012: 16
- FWCI
- 5.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Regulatory, Integrative and Comparative Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (5T3 AG 021890 02, P01 AG-20591, P01AG020591, T32AG021890)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Keywords
- skeletal muscle atrophy, denervation, mitochondrial reactive oxygen species, oxidative stress, sciatic nerve transection, aging, amyotrophic lateral sclerosis, muscle mass loss, hindlimb muscles
- MeSH terms
- Superoxide Dismutase-1, Amyotrophic Lateral Sclerosis, Animals, Female, Mice, Inbred C57BL, Mitochondria, Muscle, Muscle Denervation, Muscular Atrophy, Organ Size, Oxygen Consumption, Sciatic Nerve, Superoxide Dismutase, Reactive Oxygen Species, Mice, Knockout, Oxidative Stress, Muscle, Skeletal, Mice
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