Ros‐mediated activation of NF‐κB and Foxo during muscle disuse

[13] Catalase in vitro

Aebi, H. (1984) · Methods in Enzymology · doi:10.1016/s0076-6879(84)05016-3 · Cited by 25,696 · see citing works

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057 · see citing works

Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase

Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239 · see citing works

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy.

Sandri, M., Sandri, C., Gilbert, A., Skurk, C., Calabria, E., Picard, A., Walsh, K., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2004) · Cell · doi:10.1016/s0092-8674(04)00400-3 · Cited by 3,012 · see citing works

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 · see citing works

FOXO transcription factor activation by oxidative stress mediated by the small GTPase Ral and JNK

Essers, M. A., Weijzen, S., de Vries‐Smits, A. M., Saarloos, I., de Ruiter, N. D., Bos, J. L., & Burgering, B. M. T. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600476 · Cited by 798 · see citing works

Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic Control

Kamei, Y., Miura, S., SUZUKI, M. T., Kai, Y., Mizukami, J., Taniguchi, T., Mochida, K., Tomoko, H. A. T. A., Matsuda, J., Aburatani, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m400674200 · Cited by 574 · see citing works

Skeletal muscle myocytes undergo protein loss and reactive oxygen-mediated NF-κB activation in response to tumor necrosis factor α

Li, Y., Schwartz, R. J., Waddell, I. D., Holloway, B. R., & Reid, M. B. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.10.871 · Cited by 502 · see citing works

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 · see citing works

Hydrogen peroxide stimulates ubiquitin-conjugating activity and expression of genes for specific E2 and E3 proteins in skeletal muscle myotubes

Li, Y.-P., Chen, Y., Li, A. S., & Reid, M. B. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00129.2003 · Cited by 313 · see citing works

Hsp70 overexpression inhibits NF‐κB and Foxo3a transcriptional activities and prevents skeletal muscle atrophy

Judge, S. M., DODD, S. L., McClung, J. M., & Judge, A. R. (2008) · The FASEB Journal · doi:10.1096/fj.08-110163 · Cited by 288 · see citing works

Activation of an alternative NF‐ΚB pathway in skeletal muscle during disuse atrophy

Hunter, R. B., Stevenson, E. J., Koncarevic, A., Mitchell-Felton, H., Essig, D. A., & Kandarian, S. C. (2002) · The FASEB Journal · doi:10.1096/fj.01-0866com · Cited by 281 · see citing works

Induction of protein catabolism and the ubiquitin-proteasome pathway by mild oxidative stress

Gomes‐Marcondes, M. C. C., & Tisdale, M. J. (2002) · Cancer Letters · doi:10.1016/s0304-3835(02)00006-x · Cited by 249 · see citing works

TNF‐α increases ubiquitin‐conjugating activity in skeletal muscle by up‐regulating UbcH2/E2 20k

LI, Y.-P., Lecker, S. H., Chen, Y., Waddell, I. D., Goldberg, A. L., & Reid, M. B. (2003) · The FASEB Journal · doi:10.1096/fj.02-0759com · Cited by 243 · see citing works

Protein Kinase D Mediates Mitochondrion-to-Nucleus Signaling and Detoxification from Mitochondrial Reactive Oxygen Species

Störz, P., Döppler, H. R., & Toker, A. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.19.8520-8530.2005 · Cited by 237 · see citing works

Overexpression of Human Catalase Inhibits Proliferation and Promotes Apoptosis in Vascular Smooth Muscle Cells

Brown, M. R., Miller, F. J., Li, W.-G., Ellingson, A. N., Mozena, J. D., Chatterjee, P., Engelhardt, J. F., Zwacka, R. M., Oberley, L. W., Fang, X., et al. (1999) · Circulation Research · doi:10.1161/01.res.85.6.524 · Cited by 219 · see citing works

Resveratrol modulates phorbol ester-induced pro-inflammatory signal transduction pathways in mouse skin in vivo: NF-κB and AP-1 as prime targets

Kundu, J. K., Shin, Y. K., & Surh, Y. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.08.005 · Cited by 193 · see citing works

Induction of proteasome expression in skeletal muscle is attenuated by inhibitors of NF-κB activation

Wyke, S. M., Russell, S. T., & Tisdale, M. J. (2004) · British Journal of Cancer · doi:10.1038/sj.bjc.6602165 · Cited by 184 · see citing works

Skeletal muscle myocytes undergo protein loss and reactive oxygen‐mediated NF‐κB activation in response to tumor necrosis factorα

Li, Y., Schwartz, R. J., Waddell, I. D., et al. (1998) · The FASEB Journal · doi:10.1096/fasebj.12.10.971 · Cited by 154 · see citing works

Heat treatment reduces oxidative stress and protects muscle mass during immobilization

Selsby, J. T., & DODD, S. L. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00497.2004 · Cited by 147 · see citing works

Molecular mechanisms of oxidative stress resistance induced by resveratrol: Specific and progressive induction of MnSOD

Robb, E. L., Page, M. M., Wiens, B. E., & Stuart, J. A. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.12.138 · Cited by 147 · see citing works

Muscle wasting in diabetic and in tumor-bearing rats: Role of oxidative stress

Mastrocola, R., Reffo, P., Penna, F., Tomasinelli, C. E., Boccuzzi, G., Baccino, F. M., Aragno, M., & Costelli, P. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.10.047 · Cited by 115 · see citing works

Role for IκBα, but not c-Rel, in skeletal muscle atrophy

Judge, A. R., Koncarevic, A., Hunter, R. B., Liou, H., Jackman, R. W., & Kandarian, S. C. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00293.2006 · Cited by 111 · see citing works

Production of rat muscle atrophy by cast fixation.

Booth, F. W., & Kelso, J. R. (1973) · Journal of Applied Physiology · doi:10.1152/jappl.1973.34.3.404 · Cited by 101 · see citing works

Forkhead transcription factor FOXO subfamily is essential for reactive oxygen species-induced apoptosis

Nakamura, T., & Sakamoto, K. (2007) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.10.007 · Cited by 91 · see citing works

Role of reactive oxygen species in protein degradation in murine myotubes induced by proteolysis-inducing factor and angiotensin II

Russell, S. T., Eley, H. L., & Tisdale, M. J. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.04.003 · Cited by 90 · see citing works

Effect of RNA oligonucleotide targeting Foxo-1 on muscle growth in normal and cancer cachexia mice

Cm, L., Yang, Z., Liu, C.-W., Wang, R., Tien, P., Dale, R., & Sun, L.-Q. (2007) · Cancer Gene Therapy · doi:10.1038/sj.cgt.7701091 · Cited by 78 · see citing works

Mitochondrial dysfunction and sarcopenia of aging: from signaling pathways to clinical trials

Marzetti, E., Calvani, R., Cesari, M., Buford, T. W., Lorenzi, M., Behnke, B. J., & Leeuwenburgh, C. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.06.024 · Cited by 627 · see citing works

Mitochondrial quality control and muscle mass maintenance.

Romanello, V., & Sandri, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2015.00422 · Cited by 434 · see citing works

Redox Mechanism of Reactive Oxygen Species in Exercise

He, F., Li, J., Liu, Z., Chuang, C.-C., Yang, W., & Zuo, L. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00486 · Cited by 385 · see citing works

Mitochondrial pathways in sarcopenia of aging and disuse muscle atrophy

Calvani, R., Joseph, A.-M., Adhihetty, P. J., Miccheli, A., Bossola, M., Leeuwenburgh, C., Bernabei, R., & Marzetti, E. (2013) · bchm · doi:10.1515/hsz-2012-0247 · Cited by 328 · see citing works

Mitochondrial Dynamics and Mitophagy in Skeletal Muscle Health and Aging

Leduc-Gaudet, J.-P., Hussain, S. N. A., Barreiro, E., & Gouspillou, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158179 · Cited by 268 · see citing works

Mitochondrial dynamics in cancer-induced cachexia

van der Ende, M., Grefte, S., Plas, R., Meijerink, J., Witkamp, R. F., Keijer, J., & van Norren, K. (2018) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2018.07.008 · Cited by 87 · see citing works

Pgc-1α overexpression Via local transfection attenuates mitophagy pathway in muscle disuse atrophy

Kang, C., & Ji, L. L. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.12.032 · Cited by 83 · see citing works

Loss of <i>Parkin</i> impairs mitochondrial function and leads to muscle atrophy

Peker, N., Donipadi, V., Sharma, M., McFarlane, C., & Kambadur, R. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00064.2017 · Cited by 68 · see citing works

Dysregulations of mitochondrial quality control and autophagic flux at an early age lead to progression of sarcopenia in Samp8 mice

Liu, H.-W., Chang, Y.-C., Chan, Y.-C., Hu, S.-H., Liu, M.-Y., & Chang, S.-J. (2020) · Biogerontology · doi:10.1007/s10522-020-09867-x · Cited by 60 · see citing works

Master Regulators of Muscle Atrophy: Role of Costamere Components

Gorza, L., Sorge, M., Seclì, L., & Brancaccio, M. (2021) · Cells · doi:10.3390/cells10010061 · Cited by 31 · see citing works

Exercise-induced reductions in mitochondrial ADP sensitivity contribute to the induction of gene expression and mitochondrial biogenesis through enhanced mitochondrial H2O2 emission

Miotto, P. M., & Holloway, G. P. (2019) · Mitochondrion · doi:10.1016/j.mito.2018.03.003 · Cited by 30 · see citing works

Effects of running exercise during recovery from hindlimb unloading on soleus muscle fibers and their spinal motoneurons in rats

Ishihara, A., Kawano, F., Ishioka, N., et al. (2003) · Neuroscience Research · doi:10.1016/j.neures.2003.10.013 · Cited by 54 · see citing works

Muscle regeneration during hindlimb unloading results in a reduction in muscle size after reloading.

Mozdziak, P., Pulvermacher, P. M., & Schultz, E. (2001) · Journal of applied physiology · doi:10.1152/jappl.2001.91.1.183 · Cited by 86 · see citing works

Low-intensity pulsed ultrasound mitigates cognitive impairment by inhibiting muscle atrophy in hindlimb unloaded mice

Wang, W., Zhong, Y., Zhou, Y., Yu, Y., Li, J., Kang, S., Ma, Z., Fan, X., Sun, L., & Tang, L. V. (2023) · The Journal of the Acoustical Society of America · doi:10.1121/10.0020835

Long-term Physical Inactivity Exacerbates Hindlimb Unloading-induced Soleus Muscle Atrophy In Young Rats

Yoshihara, T., Tsuzuki, T., Chang, S.-W., et al. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000538663.68308.13

Gene Expression Levels of Heat Shock Proteins in the Soleus and Plantaris Muscles of Rats after Hindlimb Suspension or Spaceflight

Ishihara, A., Fujino, H., Nagatomo, F., et al. (2008) · The Journal of Physiological Sciences · doi:10.2170/physiolsci.rp000808 · Cited by 34 · see citing works