Skip to main content

Redox Homeostasis in Skeletal Muscle Aging

  • Chapter
  • First Online:
Redox Signaling and Biomarkers in Ageing

Part of the book series: Healthy Ageing and Longevity ((HAL,volume 15))

  • 779 Accesses

Abstract

Aging and age-related complications are the major social burden that contributes to disability and other poor outcomes at a higher prevalence. However, no clear attempt has been made so far in terms of diagnosis and treatment. Despite considering several theories, the reactive oxygen species (ROS) production is the one that implicates in inducing aging and age-related diseases. Nevertheless, within certain concentrations, ROS can effectively regulate various age-related signaling pathways such as PGC-1 alpha, MAPK, and mTOR. Further, the optimal ROS concentration could provide better adaptation to the cells during initial oxidative stress response which could ultimately improve the antioxidant defense system and support against age-related complications. But studies have shown that removal of ROS during antioxidants treatment or genetic increase in these antioxidants did not improve the life extension which inconclusively provides debate of ROS-induced aging and diseases. Skeletal muscle loss is one of the major hallmarks of aging and ROS, and oxidative stress is considered to be the main cause of skeletal muscle aging. This chapter discusses how ROS can influence the aging of skeletal muscle including ROS-targeted signaling in aging and age-related complications.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 119.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 159.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 159.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Ahmad F, Dixit D, Sharma V, Kumar A, Joshi SD, Sarkar C, Sen E (2016) Nrf2-driven TERT regulates pentose phosphate pathway in glioblastoma. Cell Death Dis 7(5):e2213

    Google Scholar 

  • Bakala H, Delaval E, Hamelin M, Bismuth J, Borot-Laloi C, Corman B, Friguet B (2003) Changes in rat liver mitochondria with aging. Lon protease-like reactivity and N(epsilon)-carboxymethyllysine accumulation in the matrix. Eur J Biochem 270:2295–230

    Google Scholar 

  • Bensaad K, Tsuruta A, Selak MA et al (2006) TIGAR, a p53-inducible regulator of glycolysis and apoptosis. Cell 126(1):107–120

    Article  CAS  Google Scholar 

  • Bota DA, Van Remmen H, Davies KJ (2002) Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress. FEBS Lett 532:103–106

    Article  CAS  Google Scholar 

  • Broome CS, Kayani AC, Palomero J, Dillmann WH, Mestril R, Jackson MJ, McArdle A (2006) Effect of lifelong overexpression of HSP70 in skeletal muscle on age-related oxidative stress and adaptation after nondamaging contractile activity. FASEB J 20(9):1549–1551

    Article  CAS  Google Scholar 

  • Chin ER (2004) The role of calcium and calcium/calmodulin-dependent kinases in skeletal muscle plasticity and mitochondrial biogenesis. Proc Nutr Soc 63(2):279–286

    Article  CAS  Google Scholar 

  • Cormio A, Lezza AM, Vecchiet J, Felzani G, Marangi L, Guglielmi FW, Francavilla A, Cantatore P, Gadaleta MN (2000) MtDNA deletions in aging and in nonmitochondrial pathologies. Ann N Y Acad Sci 908:299–301

    Article  CAS  Google Scholar 

  • Cortopassi GA, Arnheim N (1990) Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res 18:6927–6933

    Article  CAS  Google Scholar 

  • Degens H (2010) The role of systemic inflammation in age-related muscle weakness and wasting. Scand J Med Sci Sports 20(1):28–38

    Article  CAS  Google Scholar 

  • Delaval E, Perichon M, Friguet B (2004) Age-related impairment of mitochondrial matrix aconitase and ATPstimulated protease in rat liver and heart. Eur J Biochem 271:4559–4564

    Article  CAS  Google Scholar 

  • Dupont-Versteegden EE, Strotman BA, Gurley CM, Gaddy D, Knox M, Fluckey JD, Peterson CA (2006) Nuclear translocation of EndoG at the initiation of disuse muscle atrophy and apoptosis is specific to myonuclei. Am J Physiol Regul Integr Comp Physiol 291(6):R1730–R1740

    Article  CAS  Google Scholar 

  • Durham WJ, Aracena-Parks P, Long C, Rossi AE, Goonasekera SA, Boncompagni S, Galvan DL, Gilman CP, Baker MR, Shirokova N, Protasi F, Dirksen R, Hamilton SL (2008) RyR1 S-nitrosylation underlies environmental heat stroke and sudden death in Y522S RyR1 knockin mice. Cell 133(1):53–65

    Article  CAS  Google Scholar 

  • Edman S, Söderlund K, Moberg M, Apró W, Blomstrand E (2019) mTORC1 Signaling in Individual Human Muscle Fibers Following Resistance Exercise in Combination With Intake of Essential Amino Acids. Front Nutr 25(6):96. https://doi.org/10.3389/fnut.2019.00096

    Article  CAS  Google Scholar 

  • Eriksen CS, Garde E, Reislev NL, Wimmelmann CL, Bieler T, Ziegler AK, Gylling AT, Dideriksen KJ, Siebner HR, Mortensen EL, Kjaer M (2016) Physical activity as intervention for age-related loss of muscle mass and function: protocol for a randomised controlled trial (the LISA study). BMJ Open 6(12):e012951

    Google Scholar 

  • Farout L, Friguet B (2006) Proteasome function in aging and oxidative stress: implications in protein maintenance failure. Antioxid Redox Signal 8(1–2):205–216

    Article  CAS  Google Scholar 

  • Gianni P, Jan KJ, Douglas MJ, Stuart PM, Tarnopolsky MA (2004) Oxidative stress and the mitochondrial theory of aging in human skeletal muscle. Exp Gerontol 39(9):1391–1400

    Article  CAS  Google Scholar 

  • Gomez-Cabrera MC, Domenech E, Viña J (2008) Moderate exercise is an antioxidant: upregulation of antioxidant genes by training. Free Radical Biol Med 44(2):126–131

    Article  CAS  Google Scholar 

  • Harman D (1956) Aging: a theory based on free radical and radiation chemistry. J Gerontol 11(3):298–300

    Article  CAS  Google Scholar 

  • Hiona A, Sanz A, Kujoth GC, Pamplona R, Seo AY, Hofer T, Someya S, Miyakawa T, Nakayama C, Samhan-Arias AK, Servais S, Barger JL, Portero-Otín M, Tanokura M, Prolla TA, Leeuwenburgh C (2010) Mitochondrial DNA mutations induce mitochondrial dysfunction, apoptosis and sarcopenia in skeletal muscle of mitochondrial DNA mutator mice. PLoS One 7;5(7):e11468

    Google Scholar 

  • Jackson MJ, McArdle A (2011) Age-related changes in skeletal muscle reactive oxygen species generation and adaptive responses to reactive oxygen species. J Physiol 589:2139–2145

    Article  CAS  Google Scholar 

  • Jang YC, Rodriguez K, Lustgarten MS, Muller FL, Bhattacharya A, Pierce A, Choi JJ, Lee NH, Chaudhuri A, Richardson AG, Van Remmen H (2020) Superoxide-mediated oxidative stress accelerates skeletal muscle atrophy by synchronous activation of proteolytic systems. Geroscience 42(6):1579–1591

    Article  CAS  Google Scholar 

  • Ji LL (2015) Redox signaling in skeletal muscle: role of aging and exercise. Adv Physiol Educ 39(4):352–359

    Article  Google Scholar 

  • Ji LL, Gomez-Cabrera MC, Vina J (2006) Exercise and hormesis: activation of cellular antioxidant signaling pathway. Ann N Y Acad Sci 1067:425–435

    Article  CAS  Google Scholar 

  • Kregel KC, Zhang HJ (2007) An integrated view of oxidative stress in aging: basic mechanisms, functional effects, and pathological considerations. Am J Physiol Regul Integr Comp Physiol 292(1):R18-36

    Article  CAS  Google Scholar 

  • Larsson L, Degens H, Li M, Salviati L, Lee YI, Thompson W, Kirkland JL, Sandri M (2019) Sarcopenia: aging-related loss of muscle mass and function. Physiol Rev 99(1):427–511

    Article  Google Scholar 

  • Lennicke C, Cochemé HM (2020) Redox signalling and ageing: insights from Drosophila. Biochem Soc Trans 29;48(2):367–377

    Google Scholar 

  • Lindsey ME, Tarr MA (2000) Quantitation of hydroxyl radical during fenton oxidation following a single addition of iron and peroxide. Chemosphere 41(3):409–417

    Article  CAS  Google Scholar 

  • Luo J, Mills K, le Cessie S, Noordam R, van Heemst D (2020) Ageing, age-related diseases and oxidative stress: what to do next? Ageing Res Rev 57:100982

    Google Scholar 

  • Marcillat O, Zhang Y, Lin SW, Davies KJ (1988) Mitochondria contain a proteolytic system which can recognize and degrade oxidatively-denatured proteins. Biochem J 254:677–683

    Article  CAS  Google Scholar 

  • Morsch ALBC, Wisniewski E, Luciano TF, Comin VH, Silveira GB, Marques SO, Thirupathi A, Silveira Lock PC, De Souza CT (2019) Cigarette smoke exposure induces ROS-mediated autophagy by regulating sestrin, AMPK, and mTOR level in mice. Redox Rep 24(1):27–33

    Article  CAS  Google Scholar 

  • Nascimento CM, Ingles M, Salvador-Pascual A, Cominetti MR, Gomez-Cabrera MC, Viña J (2019) Sarcopenia, frailty and their prevention by exercise. Free Radic Biol Med 132:42–49

    Article  CAS  Google Scholar 

  • Picca A, Calvani R (2021) Molecular mechanism and pathogenesis of sarcopenia: an overview. Int J Mol Sci 22(6):3032

    Article  Google Scholar 

  • Powers SK, Deminice R, Ozdemir M, Yoshihara T, Bomkamp MP, Hyatt H (2020) Exercise-induced oxidative stress: friend or foe? J Sport Health Sci 9(5):415–425

    Article  Google Scholar 

  • Prunonosa Cervera I, Gabriel BM, Aldiss P, Morton NM (2021) The phospholipase A2 family’s role in metabolic diseases: focus on skeletal muscle. Physiol Rep 9(1):e14662

    Google Scholar 

  • Radak Z, Torma F, Berkes I, Goto S, Mimura T, Posa A, Balogh L, Boldogh I, Suzuki K, Higuchi M, Koltai E (2019) Exercise effects on physiological function during aging. Free Radic Biol Med 20(132):33–41

    Article  Google Scholar 

  • Rasmussen UF, Krustrup P, Kjaer M, Rasmussen HN (2003) Experimental evidence against the mitochondrial theory of aging. A study of isolated human skeletal muscle mitochondria. Exp Gerontol 38:877–886

    Article  CAS  Google Scholar 

  • Redman LM, Smith SR, Burton JH, Martin CK, Il’yasova D, Ravussin E (2018) Metabolic slowing and reduced oxidative damage with sustained caloric restriction support the rate of living and oxidative damage theories of aging. Cell Metab 3;27(4):805–815.e4

    Google Scholar 

  • Sakellariou GK, Vasilaki A, Palomero J, Kayani A, Zibrik L, McArdle A, Jackson MJ (2013) Studies of mitochondrial and nonmitochondrial sources implicate nicotinamide adenine dinucleotide phosphate oxidase(s) in the increased skeletal muscle superoxide generation that occurs during contractile activity. Antioxid Redox Signal 18(6):603–621

    Article  CAS  Google Scholar 

  • Schubert J, Wilmer JW (1991) Does hydrogen peroxide exist “free” in biological systems? Free Radic Biol Med 11(6):545–555

    Article  CAS  Google Scholar 

  • Scicchitano BM, Pelosi L, Sica G, Musarò A (2018) The physiopathologic role of oxidative stress in skeletal muscle. Mech Ageing Dev 170:37–44

    Article  CAS  Google Scholar 

  • Thirupathi A, da Silva Pieri BL, Queiroz JAMP, Rodrigues MS, de Bem SG, de Souza DR, Luciano TF, Silveira PCL, De Souza CT (2019) Strength training and aerobic exercise alter mitochondrial parameters in brown adipose tissue and equally reduce body adiposity in aged rats. J Physiol Biochem 75(1):101–108

    Article  CAS  Google Scholar 

  • Tilstra JS, Clauson CL, Niedernhofer LJ, Robbins PD (2011) NF-κB in aging and disease. Aging Dis 2(6):449–465

    PubMed  PubMed Central  Google Scholar 

  • Viña J, Salvador-Pascual A, Tarazona-Santabalbina FJ, Rodriguez-Mañas L, Gomez-Cabrera MC (2016) Exercise training as a drug to treat age associated frailty. Free Radic Biol Med 98:159–164

    Article  Google Scholar 

  • Zainal TA, Oberley TD, Allison DB, Szweda LI, Weindruch R (2000) Caloric restriction of rhesus monkeys lowers oxidative damage in skeletal muscle. FASEB J 14:1825–183610973932

    Article  CAS  Google Scholar 

  • Zorov DB, Juhaszova M, Sollott SJ (2014) Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. Physiol Rev 94(3):909–950

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors would like to acknowledge Mr. Kishore Kumar who helped in editing the manuscript.

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Ethics declarations

Disclosure of Potential Conflicts of Interest:

The authors declare that there is no conflict of interest to declare.

Research Involving Human Participants and/or Animals:

This study does not involve any human and animals’ participants.

Informed Consent:

Informed consent was obtained from all the individual participants in the study.

Rights and permissions

Reprints and permissions

Copyright information

© 2022 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Thirupathi, A., Pinho, R.A., Gu, Y. (2022). Redox Homeostasis in Skeletal Muscle Aging. In: Çakatay, U. (eds) Redox Signaling and Biomarkers in Ageing. Healthy Ageing and Longevity, vol 15. Springer, Cham. https://doi.org/10.1007/978-3-030-84965-8_5

Download citation

Publish with us

Policies and ethics