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Effects of Aging on Mitochondrial DNA Copy Number and Cytochromec Oxidase Gene Expression in Rat Skeletal Muscle, Liver, and Heart
Open accessAbstract
Mitochondrial DNA (mtDNA) deletions and mutations have been reported to occur with aging in various tissues. To determine the functional impact of these changes, we measured mtDNA copy number, mitochondria-encoded cytochrome c oxidase (COX) subunit I and III transcript levels, and COX enzyme activity in skeletal muscles (medial and lateral gastrocnemius and soleus), liver, and heart in 6- and 27-month-old rats. Substantial age-related reductions of mtDNA copy number occurred in skeletal muscle groups (-23-40%, p < 0.03) and liver (-50%, p < 0.01) but not in the heart. The decline in mtDNA was not associated with reduced COX transcript levels in tissues with high oxidative capacities such as red soleus muscle or liver, while transcript levels were reduced with aging in the less oxidative mixed fiber gastrocnemius muscle (-17-22%, p < 0.05). Consistent with transcript levels, COX activity also remained unchanged in aging liver and heart but declined with age in the lateral gastrocnemius (-32%, p < 0.05). Thus, the effects of aging on mitochondrial gene expression are tissue-specific. A substantial age-related decline in mtDNA copy number proportional to tissue oxidative capacities is demonstrated in skeletal muscle and liver. mtDNA levels are in contrast preserved in the aging heart muscle, presumably due to its incessant aerobic activity. Reduced mtDNA copy number has no major effects on mitochondrial encoded transcript levels and enzyme activities in various tissues under these base-line study conditions. In contrast, maintenance of mitochondrial transcript levels that may be linked to oxidative metabolism and energy demand appears to be the main determinant of mitochondrial oxidative capacity in aging tissues.
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“Age-associated alterations have been reported in skeletal muscle at both transcriptional and functional levels of mitochondrial gene expression (27).”
From Discovering pathways of sarcopenia in older adults: a role for insulin resistance on mitochondria dysfunction (2011) · cites this paper as [27]
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“Multiple groups have reported a decrease in skeletal muscle mitochondrial content and function with age.126-128”
From Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications (2021) · cites this paper as [127]
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Cites
Molecular cloning: A laboratory manual
Deininger, P. L. (1990) · Analytical Biochemistry · doi:10.1016/0003-2697(90)90595-z · Cited by 84,684
tRNA punctuation model of RNA processing in human mitochondria
Ojala, D., Montoya, J., & Attardi, G. M. (1981) · Nature · doi:10.1038/290470a0 · Cited by 2,561
Adaptations of skeletal muscle to endurance exercise and their metabolic consequences
Holloszy, J. O., & Coyle, E. F. (1984) · Journal of Applied Physiology · doi:10.1152/jappl.1984.56.4.831 · Cited by 1,985
Harman, D. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.11.7124 · Cited by 1,915
Mitochondrial Genetics: A Paradigm for Aging and Degenerative Diseases?
Wallace, D. C. (1992) · Science · doi:10.1126/science.1533953 · Cited by 1,262
Muscle fiber type composition of the rat hindlimb
Armstrong, R. B., & Phelps, R. O. (1984) · American Journal of Anatomy · doi:10.1002/aja.1001710303 · Cited by 1,004
Cardiovascular regulatory mechanisms in advanced age.
Lakatta, E. G. (1993) · Physiological Reviews · doi:10.1152/physrev.1993.73.2.413 · Cited by 791
Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing
Trounce, I., Byrne, E., & Marzuki, S. (1989) · The Lancet · doi:10.1016/s0140-6736(89)92143-0 · Cited by 730
Effect of age on in vivo rates of mitochondrial protein synthesis in human skeletal muscle
Rooyackers, O. E., Adey, D. B., Ades, P. A., & Nair, K. S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15364 · Cited by 564
Self-citationKarlson, P. (1974) · Biochemical Education · doi:10.1016/0307-4412(74)90015-6 · Cited by 541
Flagged first, then by citations
Research works printed but not linked: 4
- Murakami, 1994, Am. J. Physiol., 267, E388
- Ji, 1990, Am. J. Physiol., 258, R918
- Ji, 1991, Am. J. Physiol., 261, R386
- Fu, 1998, Am. J. Physiol., 275, E1023
Cited by
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Comparative Skeletal Muscle Aging
Marcinek, D. J., Wanagat, J., & Villarin, J. J. (2009) · Springer eBooks · doi:10.1007/978-90-481-3465-6_13 · Cited by 3
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Zhang, S. B., Maguire, D., Zhang, M., Zhang, A., Zhang, L., Swarts, S. G., & Okunieff, P. G. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-7411-1_34 · Cited by 3
Gasparino, E., Vesco, A. P. D., Guimarães, S. E. F., da Silva, S. C. C., Marcato, S. M., Neto, A. R. D. O., & Sousa, K. R. S. (2012) · Genetics and Molecular Research · doi:10.4238/2012.august.6.2 · Cited by 3
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Kaira, M., Walia, V., & Garg, M. (2022) · Springer eBooks · doi:10.1007/978-981-16-7606-2_10 · Cited by 3
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Lee, H. K. (2005) · Oxidative stress and disease · doi:10.1201/9781420028843.ch8 · Cited by 3
Yu, X., Chen, L., He, X., Han, Y., Huang, Y., Wu, J., Sha, R., & Borjigin, G. (2025) · Animal Bioscience · doi:10.5713/ab.24.0706 · Cited by 3
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Ayala‐Peña, S., & Torres‐Ramos, C. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405933-7.00004-4 · Cited by 2
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Short, K. R. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00606.2003 · Cited by 2
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Garros, R. F. (2017) · Spiral (Imperial College London) · doi:10.25560/68036 · Cited by 2
Zhang, R., Du, J., Xiao, Z., Jiang, Y., Weng, Q., & Jin, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1168394/v1 · Cited by 2
Masenga, S. K., Murphy, A. C., Venkhatesh, P., Vue, Z., Kadam, A. A., Marshall, A. G., Rodriguez, B., Scudese, E., Jenkins, B. C., Crabtree, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.20.599846 · Cited by 2
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Chan, D., Jhuang, J.-H., Chang, F.-Y., Sheu, M., Lan, K., & Liu, S.-H. (2026) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2026.110774 · Cited by 1
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Historical perspective of matrix metalloproteases
Pulkoski‐Gross, A. (2011) · Frontiers in Bioscience-Scholar · doi:10.2741/429 · Cited by 1
Murase, T. (2012) · Tea in Health and Disease Prevention · doi:10.1016/b978-0-12-384937-3.00060-4 · Cited by 1
Bauer, B. S., Forsyth, G. W., Sandmeyer, L. S., & Grahn, B. H. (2010) · American Journal of Veterinary Research · doi:10.2460/ajvr.71.4.454 · Cited by 1
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Ogborn, D. I. (2013) · MacSphere (McMaster University) · doi:10.71548/15322 · Cited by 1
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Marı́n-Garcı́a, J., Goldenthal, M. J., & Moe, G. W. P. L. (2007) · Springer eBooks · doi:10.1007/978-0-387-74072-0_6
Dietary and exercise manipulation of skeletal muscle function in older humans
Smith, G. N. (2010) · Victoria University Research Repository (Victoria University)
The Role of Mitochondrial DNA in Tumorigenesis
Yeung, K. Y., Dickinson, A., & John, J. C. S. (2012) · Humana Press eBooks · doi:10.1007/978-1-62703-101-1_6
Bauer, B. S. (2008) · University Library - University of Saskatchewan (University of Saskatchewan)
MacKrell, J. G. (2013) · Deep Blue (University of Michigan)
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Marı́n-Garcı́a, J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4599-9_13
Edgar, D., & Trifunović, A. (2007) · Springer eBooks · doi:10.1007/978-88-470-0376-7_7
Evaluation of the cell-free mitochondrial DNA quantity in plasma as an aging biomarker candidate
Nevalainen, T. (2012) · Tampere University Institutional Repository (Tampere University)
Leslie, M. (2004) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2004.43.ns8
Age-induced muscle atrophy and increase in fatigue resistance
Masuda, S., Takakura, H., Kato, H., & Izawa, T. (2014) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.3.435
Anti-Aging Medicine LiteratureWatch
Pawelec, G. (1998) · Rejuvenation Research · doi:10.1089/rej.1.1998.1.275
Chandrashekar, P. (2016) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/67320
Mitochondria, Aging, and Disease
Salvioli, S., Bonafè, M., Barbi, C., Capri, M., Monti, D., & Franceschi, C. (2003) · Oxidative stress and disease · doi:10.1201/9780203912874.ch7
Skeletal muscle regeneration and the role of Sirtuin 1
Bennett, B. T. (2013) · doi:10.33915/etd.4952
Effects of Resistance Training on aged Skeletal Muscle and Mitochondrial Function
Flack, K. D. (2014) · VTechWorks (Virginia Tech)
The Role of p38 MAPK in Protein Homeostasis and Aging
Ryan, S. M. (2016) · Digital Commons - DU (University of Denver)
Marı́n-Garcı́a, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00019-6
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Mumford, P. W. (2019)
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Geden, M. J. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/qbvf-hg05
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Marcus, R. L., Reidy, P. T., & LaStayo, P. C. (2019) · Elsevier eBooks · doi:10.1016/b978-0-323-60912-8.00016-6
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Davidson, R. L. (2021) · Science Insights · doi:10.15354/si.21.re201
Anti-Aging Medicine LiteratureWatch
(2000) · Rejuvenation Research · doi:10.1089/10945450050164808
Anti-Aging Medicine LiteratureWatch
Pawelec, G. (2000) · Rejuvenation Research · doi:10.1089/rej.1.2000.3.207
Faculty Opinions recommendation of Mitochondrial function as a determinant of life span.
Jammes, Y. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1448967.926071
The Aging Heart: A Post-Genomic Appraisal
Marı́n-Garcı́a, J. (2007) · Elsevier eBooks · doi:10.1016/b978-012373698-7/50019-x
Quiriarte, H. D. (2021) · Louisiana State University · doi:10.31390/gradschool_theses.5265
Rösch, A. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10109
Sadeesh, E. M., & Malik, A. (2023) · Research Square · doi:10.21203/rs.3.rs-3647029/v1
Kolonics, A., Kawamura, T., Szipöcs, R., & Radak, Z. O. (2024) · Single Molecule Spectroscopy and Superresolution Imaging · doi:10.1117/12.3005632
Investigation and description of the New Brain and New Mind hypotheses
Klinedinst, B. S. (2021) · doi:10.31274/td-20240329-457
Zhang, R., Du, J., Xiao, Z., Jiang, Y., Jin, L., & Weng, Q. (2022) · Figshare · doi:10.6084/m9.figshare.20064457
Analysis of Adipose Tissue Characteristics and Lipid Metabolism in Natural Grazing Mongolian CattlePreprint
Yu, X., Chen, L., He, X., Han, Y., Huang, Y., Wu, J., Sha, R., & Borjigin, G. (2024) · Preprints.org · doi:10.20944/preprints202408.1617.v1
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Park, M. Y., Kim, D. E., Seok, M.-K., Whang, K. Y., & Kim, J.-M. (2026) · Scientific Reports · doi:10.1038/s41598-026-40724-y
Emerging therapeutic approaches in neurobiology of type 2 diabetes
Kumar, U., Garg, S., Shrivastav, A., Sharma, B., Arora, B., Sahu, B., & Gupta, M. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-32848-0.00023-6
Mitochondria, neurosteroids and biological rhythms : implications in health and disease states
Grimm, A. (2015) · theses.fr (ABES) · doi:10.70675/8aac5aa9z77cdz49bdz9cf5z0ff0b5dd0f84
Ovarian aging: Mechanisms and strategies to extend reproductive lifespan
Liu, Y., Wang, Z., Yang, M., Lin, Y., Huo, R., Hu, Z., & Li, J. (2026) · Chinese Medical Journal BioMed · doi:10.65457/cmjbm-2026-0004 · Cited by 1
Exercise-induced mitochondrial remodeling in energy-demanding organs during aging
Zhou, Z., Gao, J., Wang, M., & Zhang, H. (2026) · iScience · doi:10.1016/j.isci.2026.116791 · Cited by 1
Tarai, S., Thyagarajan, D., Srinivasan, G., & Mangalagowri, A. (2024) · Indian Journal of Poultry Science · doi:10.5958/0974-8180.2024.00010.7
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Guescini, M., Stocchi, L., Loreto, C. D., Fatone, C., Feo, P. D., & Stocchi, V. (2007) · Springer eBooks · doi:10.1007/978-88-470-0376-7_5
Metadata
- Authors
- Barazzoni, R., Short, K. R., & Nair, K. S.
- Affiliations
- Mayo Clinic (US)
- Corresponding author
- Nair, K.Sreekumaran
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2000-02
- Volume
- 275
- Issue
- 5
- Pages
- 3343-3347
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2011919513
- Cited by
- 367
- References
- 37
- Citations by year
- 2026: 5 · 2025: 4 · 2024: 7 · 2023: 8 · 2022: 18 · 2021: 18 · 2020: 13 · 2019: 15 · 2018: 11 · 2017: 12 · 2016: 12 · 2015: 11 · 2014: 17 · 2013: 17 · 2012: 20
- FWCI
- 4.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (R0 AG 09531, R01AG009531)
- National Center for Research Resources (RR-00585, M01RR000585)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Keywords
- aging, mitochondrial DNA copy number, cytochrome c oxidase, mitochondrial gene expression, skeletal muscle, liver, heart, oxidative capacity, tissue-specific aging, gastrocnemius, soleus muscle
- MeSH terms
- Aging, Animals, Electron Transport Complex IV, DNA, Mitochondrial, Heart, Liver, Male, Rats, Inbred F344, Gene Expression, Muscle, Skeletal, Rats
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