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Training-Induced Changes in Mitochondrial Content and Respiratory Function in Human Skeletal Muscle
Open accessAbstract
A sedentary lifestyle has been linked to a number of metabolic disorders that have been associated with sub-optimal mitochondrial characteristics and an increased risk of premature death. Endurance training can induce an increase in mitochondrial content and/or mitochondrial functional qualities, which are associated with improved health and well-being and longer life expectancy. It is therefore important to better define how manipulating key parameters of an endurance training intervention can influence the content and functionality of the mitochondrial pool. This review focuses on mitochondrial changes taking place following a series of exercise sessions (training-induced mitochondrial adaptations), providing an in-depth analysis of the effects of exercise intensity and training volume on changes in mitochondrial protein synthesis, mitochondrial content and mitochondrial respiratory function. We provide evidence that manipulation of different exercise training variables promotes specific and diverse mitochondrial adaptations. Specifically, we report that training volume may be a critical factor affecting changes in mitochondrial content, whereas relative exercise intensity is an important determinant of changes in mitochondrial respiratory function. As a consequence, a dissociation between training-induced changes in mitochondrial content and mitochondrial respiratory function is often observed. We also provide evidence that exercise-induced changes are not necessarily predictive of training-induced adaptations, we propose possible explanations for the above discrepancies and suggestions for future research.
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“Training volume plays a crucial role in influencing changes in mitochondrial content, whereas relative exercise intensity is a key factor in determining alterations in mitochondrial respiratory function [68].”
From Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis (2025) · cites this paper as [68]
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Cites
Global quantification of mammalian gene expression control
Schwanhäusser, B., Busse, D., Li, N., Dittmar, G., Schuchhardt, J., Wolf, J., Chen, W., & Selbach, M. (2011) · Nature · doi:10.1038/nature10098 · Cited by 6,566
Åstrand, P., & Rodahl, K. (1970) · Andalas University Repository (Andalas University) · Cited by 4,434
(1982) · Cited by 3,737
Mitochondria: In Sickness and in Health
Nunnari, J., & Suomalainen, A. (2012) · Cell · doi:10.1016/j.cell.2012.02.035 · Cited by 3,479
Ezzati, M., López, A. D., Rodgers, A., & Murray, C. J. L. (2004) · Cited by 3,319
Mitochondrial dysfunction and type 2 diabetes
Lowell, B. B., & Shulman, G. I. (2005) · Science · doi:10.1126/science.1104343 · Cited by 2,070
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
Physiological adaptations to low-volume, high-intensity interval training in health and disease
Gibala, M. J., Little, J. P., MacDonald, M. J., & Hawley, J. A. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.224725 · Cited by 1,744
p53 Regulates Mitochondrial Respiration
Matoba, S., Kang, J.-G., Patino, W. D., Wragg, A., Boehm, M., Gavrilova, O., Hurley, P. J., Bunz, F., & Hwang, P. M. (2006) · Science · doi:10.1126/science.1126863 · Cited by 1,650
Biochemical Adaptations in Muscle
Holloszy, J. O. (1967) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96046-1 · Cited by 1,517
Research works printed but not linked: 1
- World Health Organization. Global health risks: mortality and burden of disease attributable to selected major risks. Geneva: World Health Organization; 2009.
Cited by
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Smith, J. A. B., Murach, K. A., Dyar, K. A., & Zierath, J. R. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00606-x · Cited by 342
Egan, B., & Sharples, A. P. (2023) · Physiological Reviews · doi:10.1152/physrev.00054.2021 · Cited by 278
ATAKAN, M. M., Li, Y., Koşar, Ş. N., Turnagöl, H. H., & Yan, X. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18137201 · Cited by 334
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Furrer, R., Hawley, J. A., & Handschin, C. (2023) · Physiological Reviews · doi:10.1152/physrev.00017.2022 · Cited by 253
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Glancy, B. C., Kane, D. A., Kavazis, A. N., Goodwin, M. L., Willis, W. T., & Gladden, L. B. (2020) · The Journal of Physiology · doi:10.1113/jp278930 · Cited by 216
“Mammalian myocytes can respond to endurance training with nearly 2-fold increases in mitochondrial abundance (e.g. Holloszy & Coyle, 1984; Granata et al. 2018), leading to significant decreases in lactate production, increased removal, and decreased net accumulation.”
BackgroundBishop, D. J., Botella, J., Genders, A. J., Lee, M. J.-C., Saner, N. J., Kuang, J., Yan, X., & Granata, C. (2019) · Physiology · doi:10.1152/physiol.00038.2018 · Cited by 180
Self-citationBurtscher, J., Millet, G. P., Place, N., Kayser, B., & Zanou, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126479 · Cited by 164
“Higher exercise volumes [70], multiple exercise sessions per day, and elevated intensity [69] are associated with increasing stimulation of mitochondrial protein synthesis and mitochondrial fusion, improving structural and functional mitochondrial features.”
BackgroundMølmen, K. S., Almquist, N. W., & Skattebo, Ø. (2025) · Sports Medicine · doi:10.1007/s40279-024-02120-2 · Cited by 123
“Granata and colleagues [11] pooled the results from 58 exercise training studies and found no significant association between exercise training intensity (% of Wmax) and change in mitochondrial content, as assessed by either CS activity or MvD.”
InfluentialHuertas, J. R., Casuso, R. A., Hernansanz‐Agustín, P., & Cogliati, S. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7058350 · Cited by 106
Scaricamazza, S., Salvatori, I., Giacovazzo, G., Loeffler, J., René, F., Rosina, M., Quessada, C., Proietti, D., Heil, C., Rossi, S., et al. (2020) · iScience · doi:10.1016/j.isci.2020.101087 · Cited by 98
Groennebaek, T., Jespersen, N. R., Jakobsgaard, J. E., Sieljacks, P., Wang, J., Rindom, E., Musci, R. V., Bøtker, H. E., Hamilton, K. L., Miller, B. F., et al. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01796 · Cited by 88
“Aging, prolonged inactivity, and several chronic diseases negatively affect skeletal muscle mitochondrial and myofibrillar properties (Clark, 2009; Zizola and Schulze, 2013; Gram et al., 2014; Rontoyanni et al., 2017; Granata et al., 2018; Holloway et al., 2018).”
BackgroundGranata, C., Caruana, N. J., Botella, J., Jamnick, N. A., Huynh, K., Kuang, J., Janssen, H. A., Reljic, B., Mellett, N. A., Laskowski, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27153-3 · Cited by 93
Self-citationFiorenza, M., Lemminger, A. K., Marker, M., Eibye, K., Iaia, F. M., Bangsbo, J., & Hostrup, M. (2019) · The FASEB Journal · doi:10.1096/fj.201900106rrr · Cited by 69
“SET was chosen in view of evidence indicating its effectiveness to increase mitochondrial respiratory capacity, up-regulate mitochondrial proteins, and enhance performance (7, 33, 34).”
BackgroundMethodRosenblat, M. A., Granata, C., & Thomas, S. G. (2022) · Sports Medicine · doi:10.1007/s40279-021-01624-5 · Cited by 73
“[23] study included HIIT, SIT, and MICT in the same analysis, whereas the analysis in the current review divided exercise types into different groups, and did not include studies assessing MICT.”
BackgroundMethodInfluentialSelf-citationBishop, D. J., Botella, J., & Granata, C. (2019) · The Journal of Physiology · doi:10.1113/jp277634 · Cited by 68
“There was, however, no significant association between exercise intensity and changes in mitochondrial content (as assessed by either CS activity or TEM; Granata et al. 2018b).”
BackgroundResultInfluentialSelf-citationMetabolic Health—The Role of Adipo-Myokines
Gräf, C., & Ferrari, N. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246159 · Cited by 70
“It seems critical that an (exercise) stimulus needs to pass a certain threshold level to be effective [99], but this assumption may be based on a methodological problem.”
BackgroundChristiansen, D., Eibye, K., Hostrup, M., & Bangsbo, J. (2020) · The Journal of Physiology · doi:10.1113/jp279554 · Cited by 67
“maximal ex vivo respiration) with high-intensity training have been reported without a concurrent upregulation of mitochondrial protein expression in human skeletal muscle (Granata et al. 2018).”
BackgroundBurtscher, J., Burtscher, M., & Millet, G. P. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101976 · Cited by 67
“Importantly, remodeling of mitochondrial functions can be controlled by the selection of different types of exercise, duration and intensity [123,136], in theory enabling targeted exercise intervention to”
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Rothschild, J. A., & Bishop, D. J. (2019) · Sports Medicine · doi:10.1007/s40279-019-01185-8 · Cited by 64
Self-citationMalta, E. D. S., Dutra, Y. M., Broatch, J. R., Bishop, D. J., & Zagatto, A. M. (2020) · Sports Medicine · doi:10.1007/s40279-020-01362-0 · Cited by 60
Self-citationThe influence of aerobic exercise on mitochondrial quality control in skeletal muscle
Philp, A. M., Saner, N. J., Lazarou, M., Ganley, I. G., & Philp, A. (2020) · The Journal of Physiology · doi:10.1113/jp279411 · Cited by 62
The role of mitochondria in iron overload-induced damage
Zhao, Y., Yang, M., & Liang, X. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05740-4 · Cited by 67
Polarized Training Is Not Optimal for Endurance Athletes
BURNLEY, M., BEARDEN, S. E., & JONES, A. M. (2022) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002869 · Cited by 55
Ferguson, R. A., Mitchell, E. A., Taylor, C. W., Bishop, D. J., & Christiansen, D. (2021) · Experimental Physiology · doi:10.1113/ep089280 · Cited by 59
“Mitochondrial biogenesis can be defined as the making of new components of the mitochondrial reticulum (Granata et al., 2018) and can include changes in mitochondrial content, mitochondrial respiratory function or other aspects of mitochondrial quality, such as the density of the cristae or…”
Self-citationExercise twice‐a‐day potentiates markers of mitochondrial biogenesis in men
Andrade‐Souza, V. A., Ghiarone, T., Sansonio, A., Silva, K. A. S., Tomazini, F., Arcoverde, L., Fyfe, J. J., Perri, E., Saner, N. J., Kuang, J., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201901207rr · Cited by 53
Self-citationLi, J., Zhang, S., Li, C., Zhang, X., Shan, Y., Zhang, Z., Hai, B., & Zhang, Y. (2024) · Scientific Reports · doi:10.1038/s41598-024-72088-6 · Cited by 59
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Genders, A. J., Holloway, G. P., & Bishop, D. J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186948 · Cited by 51
“Exercise-induced improvements in insulin resistance were recently shown to disappear after four non-exercise days [63], while other studies have reported a much slower decline in mitochondrial content [49].”
BackgroundSelf-citationLiu, S., Yu, C., Xie, L., Niu, Y., & Fu, L. (2021) · The Journals of Gerontology Series A · doi:10.1093/gerona/glab029 · Cited by 51
Common methods in mitochondrial research (Review)
Yin, Y., & Shen, H. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5182 · Cited by 52
“copy (EM) has become the central tool for observing organelles in eukaryotic cells and is the gold standard for observing mito‐ chondrial structure (60).”
MethodPhysiological basis of interval training for performance enhancement
Gibala, M. J. (2020) · Experimental Physiology · doi:10.1113/ep088190 · Cited by 54
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Zanou, N., Dridi, H., Reiken, S. R., de Lima, T. I., Donnelly, C., Marchi, U. D., Ferrini, M., Vidal, J., Sittenfeld, L. R., Feige, J. N., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27422-1 · Cited by 46
Schader, J. F., Haid, M., Cecil, A., Schoenfeld, J., Halle, M., Pfeufer, A., Prehn, C. P., Adamski, J., Nieman, D. C., & Scherr, J. (2020) · Metabolites · doi:10.3390/metabo10030087 · Cited by 44
“High-intensity interval training improves mitochondrial respiratory function [16] whereas endurance training increases the mitochondrial content [17].”
BackgroundDreher, S. I., Irmler, M., Pivovarova‐Ramich, O., Kessler, K., Jürchott, K., Sticht, C., Fritsche, L., Schneeweiß, P., Machann, J., Pfeiffer, A. F. H., et al. (2023) · International Journal of Obesity · doi:10.1038/s41366-023-01271-y · Cited by 43
“It is known that in SM mitochondrial respiration is induced in response to training [12, 23, 48] which we confirmed in our study accompanied by the strong acute induction of mitochondrial marker PGC1α expression in SM as an acute response to exercise bouts.”
BackgroundBishop, D. J., Lee, M. J.-C., & Picard, M. A. (2024) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022724-104836 · Cited by 46
Self-citationWang, Y., Li, P., Cao, Y., Liu, C., Wang, J., & Wu, W. (2022) · Aging and Disease · doi:10.14336/ad.2022.0603 · Cited by 41
“Longterm regular exercise can increase mitochondrial number and biogenesis, resulting in good adaptation of muscle cells [81].”
BackgroundGenders, A. J., Martin, S. D., McGee, S. L., & Bishop, D. J. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00214.2018 · Cited by 40
Self-citationStocks, B., Dent, J. R., Ogden, H. B., Zemp, M., & Philp, A. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00311.2018 · Cited by 38
Human muscular mitochondrial fusion in athletes during exercise
Huertas, J. R., Ruiz‐Ojeda, F. J., Plaza‐Díaz, J., Nordsborg, N. B., Martín‐Albo, J., Rueda‐Robles, A., & Casuso, R. A. (2019) · The FASEB Journal · doi:10.1096/fj.201900365rr · Cited by 37
“humans, SIT increases leg mitochondrial respiration without an increment inmitochondrial content (30),which could be explained by an improvement of mitochondrial function through eliminating defective organelles by fission and mitophagy (40).”
BackgroundGranata, C., Oliveira, R. S. F., Little, J. P., & Bishop, D. J. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00233.2019 · Cited by 39
Self-citationMitochondrial respiration variability and simulations in human skeletal muscle: The Gene SMART study
Jacques, M., Kuang, J., Bishop, D. J., Yan, X., Alvarez‐Romero, J., Munson, F., GARNHAM, A. P., Papadimitriou, I. D., Voisin, S. A. C., & Eynon, N. (2020) · The FASEB Journal · doi:10.1096/fj.201901997rr · Cited by 35
Self-citationLarsen, F. J., Schiffer, T. A., Zinner, C., Willis, S. J., Morales‐Álamo, D., Calbet, J. A. L., Boushel, R., & Holmberg, H. (2020) · Acta Physiologica · doi:10.1111/apha.13463 · Cited by 37
Papadimitriou, I. D., Eynon, N., Yan, X., Munson, F., Jacques, M., Kuang, J., Voisin, S. A. C., North, K. N., & Bishop, D. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-49042-y · Cited by 37
Self-citationMuscle Ionic Shifts During Exercise: Implications for Fatigue and Exercise Performance
Hostrup, M., Cairns, S. P., & Bangsbo, J. (2021) · Comprehensive physiology · doi:10.1002/cphy.c190024 · Cited by 50
The role of mitochondria in the pathophysiology and treatment of common metabolic diseases in humans
Georgiev, A., Granata, C., & Roden, M. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00035.2022 · Cited by 36
Self-citationJacob, N., So, I., Sharma, B., Marzolini, S., Tartaglia, M. C., OH, P. I., & Green, R. (2023) · Sports Medicine · doi:10.1007/s40279-023-01815-2 · Cited by 38
“Mitochondrial density can increase in response to continued exercise training [83], leading to decreased peripheral lactate accumulation [79].”
BackgroundEffects of exercise timing on metabolic health
Martínez‐Montoro, J. I., Benítez‐Porres, J., Tinahones, F. J., Ortega‐Gómez, A., & Murri, M. (2023) · Obesity Reviews · doi:10.1111/obr.13599 · Cited by 37
“It is noteworthy that exercise training is able to induce beneficial mitochondrial adaptations, including enhanced mitochondrial content, protein synthesis, oxidative capacity, or biogenesis, as well as the more efficient removal of dysfunctional/damaged mitochondria, with derived benefits in metabolic health.(118,119…”
Exercise as a tool to mitigate metabolic disease
Esteves, J. V. D. C., & Stanford, K. I. (2024) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00144.2024 · Cited by 39
Batterson, P. M., Norton, M. R., Hetz, S. E., Rohilla, S., Lindsay, K. G., Subudhi, A. W., & Jacobs, R. A. (2020) · Physiological Reports · doi:10.14814/phy2.14342 · Cited by 30
“, 2017), volume density (Granata et al., 2018; Hamaoka et al., 1996; Meinild Lundby et al., 2018), and maximal rates of respiration (Granata et al.”
BackgroundSkattebo, Ø., Bjerring, A. W., Auensen, M., Sarvari, S. I., Cumming, K. T., Capelli, C., & Hallén, J. (2020) · European Journal of Applied Physiology · doi:10.1007/s00421-020-04336-2 · Cited by 32
Boosting mitochondrial health to counteract neurodegeneration
Burtscher, J., Romani, M., Bernardo, G., Popa, T., Ziviani, E., Hummel, F. C., Sorrentino, V., & Millet, G. P. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102289 · Cited by 36
“…of exercise, as well as its intensity and frequency determines the outcomes of exercise interventions on mitochondrial functions (Egan et al., 2013; Granata et al., 2018; Harper et al., 2021): for example, regular moderate physical activity seems to be particularly suited to enhance mitochondrial…”
BackgroundMyokine, a key cytokine for physical exercise to alleviate sarcopenic obesity
Zhang, L., Lv, J., Wang, C., Ren, Y., & Ming, Y. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07821-3 · Cited by 33
Gurd, B. J., Menezes, E. S., Arhen, B. B., & Islam, H. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.05.016 · Cited by 31
Discordant skeletal muscle gene and protein responses to exercise
Bishop, D. J., Hoffman, N. J., Taylor, D. F., Saner, N. J., Lee, M. J.-C., & Hawley, J. A. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2023.08.005 · Cited by 36
Self-citationReassessing the relationship between mRNA levels and protein abundance in exercised skeletal muscles
Bishop, D. J., & Hawley, J. A. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00541-3 · Cited by 31
Self-citationToro-Román, V., Siquier-Coll, J., Bartolomé, I., Pérez, F. J. G., Muñoz, D., & Maynar-Mariño, M. (2021) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-021-00426-4 · Cited by 30
Chávez-Guevara, I. A., Hernández‐Torres, R. P., González-Rodríguez, E., Ramos‐Jiménez, A., & Amaro‐Gahete, F. J. (2022) · European Journal of Applied Physiology · doi:10.1007/s00421-022-04936-0 · Cited by 31
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 35
Mahmassani, Z. S., Reidy, P. T., McKenzie, A. I., Stubben, C., Howard, M. T., & Drummond, M. J. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01093.2018 · Cited by 29
Kuang, J., Saner, N. J., Botella, J., Lee, M. J.-C., Granata, C., Wang, Z., Yan, X., Li, J., Genders, A. J., & Bishop, D. J. (2022) · Acta Physiologica · doi:10.1111/apha.13772 · Cited by 29
Self-citationDenham, J. (2023) · Aging Cell · doi:10.1111/acel.13836 · Cited by 28
“= denotes a potential role in the healthy biological ageing conferred by exercise training; red line = acute exercise effect; blue line = chronic exercise effect. et al., 2016; Granata et al., 2018; Memme et al., 2021).”
BackgroundCardiorespiratory coordination reveals training-specific physiological adaptations
García‐Retortillo, S., Gacto, M., O’Leary, T. J., Noon, M. R., Hristovski, R., Balagué, N., & Morris, M. G. (2019) · European Journal of Applied Physiology · doi:10.1007/s00421-019-04160-3 · Cited by 32
Rosenblat, M. A., Lin, E. B., da Costa, B. R., & Thomas, S. G. (2021) · Sports Medicine · doi:10.1007/s40279-021-01457-2 · Cited by 30
“An increase in measures of mitochondrial biogenesis is an important adaption that occurs following SIT [75, 100].”
BackgroundMitochondrial Functionality in Inflammatory Pathology-Modulatory Role of Physical Activity
Casuso, R. A., & Huertas, J. R. (2021) · Life · doi:10.3390/life11010061 · Cited by 28
“In this regard, moderate exercise is able to improve skeletal muscle mitochondrial function and dynamics [54,70] even in aged skeletal muscle [55].”
BackgroundPaquette, M., Bieuzen, F., & Billaut, F. (2020) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2020.00047 · Cited by 26
“However, the most plausible explanation for the decreased SmO2 in the 200-m and 1,000-m TT is an increase in O2 consumption by the locomotor muscle, due to training-induced increase in mitochondrial content (Granata et al., 2018), resulting in improved O2 extraction.”
BackgroundReisman, E. G., Botella, J., Huang, C., Schittenhelm, R. B., Stroud, D. A., Granata, C., Chandrasiri, O. S., Ramm, G., Oorschot, V. M. J., Caruana, N. J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50632-2 · Cited by 27
Self-citationStavrinou, P. S., Astorino, T. A., Giannaki, C. D., Aphamis, G., & Bogdanis, G. C. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1553846 · Cited by 27
Takahashi, K., Kitaoka, Y., Yamamoto, K., Matsunaga, Y., & Hatta, H. (2020) · Nutrients · doi:10.3390/nu12030770 · Cited by 25
“However, although it is generally considered that mitochondrial content and respiration increase in parallel [45], this is not the case in some studies [46,47].”
ResultThe effect of HIIT vs. SIT on muscle oxygenation in trained sprint kayakers
Paquette, M., Bieuzen, F., & Billaut, F. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04743-z · Cited by 25
Harmsen, J., Kotte, M., Habets, I., Bosschee, F., Frenken, K. G., Jörgensen, J. A., de Kam, S. S., Moonen‐Kornips, E., Cissen, J., Doligkeit, D., et al. (2023) · The Journal of Physiology · doi:10.1113/jp285523 · Cited by 25
Ghiarone, T., Andrade‐Souza, V. A., LEARSI, S. K., Tomazini, F., Ataide‐Silva, T., Sansonio, A., Fernandes, M. P., Saraiva, K., de Figueiredo, R. C. B. Q., Tourneur, Y., et al. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00060.2019 · Cited by 25
Self-citationPengam, M., Amérand, A., Simon, B. M., Guernec, A., Inizan, M., & Cann-Moisan, C. (2021) · Experimental Physiology · doi:10.1113/ep089231 · Cited by 26
“If minimal exercise intensity is likely required to improve mitochondrial biogenesis (Bishop et al., 2019), training volume may also be a key determinant of training-induced changes in mitochondrial content (Granata et al., 2018).”
BackgroundMethodD’Alleva, M., Vaccari, F., Graniero, F., Giovanelli, N., Floreani, M., Fiori, F., Marinoni, M., Parpinel, M. T., & Lazzer, S. (2023) · Journal of Exercise Science & Fitness · doi:10.1016/j.jesf.2023.01.004 · Cited by 24
Li, Y., Zhao, W., & Yang, Q. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1554222 · Cited by 23
“The benefits of moderate exercise on overall health are well-established, with exercise regimens tailored to meet the specific needs of diverse populations, including individuals with various diseases, conditions, and age groups (Granata et al., 2018; Widmann et al., 2019).”
Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis
Wang, J., Jia, D., Zhang, Z., & Wang, D. (2025) · Metabolites · doi:10.3390/metabo15010059 · Cited by 23
Long-Term Physical Exercise for Preventing CKD in Older Adults
Hallan, S. I., Øvrehus, M. A., Shlipak, M. G., Potok, O. A., Romundstad, S., Aspvik, N. P., Wisløff, U., Ix, J. H., Stensvold, D., & Langlo, K. A. R. (2025) · Journal of the American Society of Nephrology · doi:10.1681/asn.0000000636 · Cited by 22
Cardinale, D. A., Gejl, K. D., Petersen, K. G., Nielsen, J., Ørtenblad, N., & Larsen, F. J. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00829.2020 · Cited by 22
Yamada, T., Kimura, I., Ashida, Y., Tamai, K., Fusagawa, H., Tohse, N., Westerblad, H., Andersson, D. C., & Sato, T. (2021) · The FASEB Journal · doi:10.1096/fj.202101204r · Cited by 22
Gejl, K. D., Andersson, E. P., Nielsen, J., Holmberg, H., & Ørtenblad, N. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00810 · Cited by 21
Eight Weeks of Physical Training Decreases 2 Years of DNA Methylation Age of Sedentary Women
Rodrigues, G. D. S., Noma, I. H. Y., Noronha, N. Y., Watanabe, L. M., Sobrinho, A. C. D. S., de Lima, J. G. R., Sae‐Lee, C., Benjamim, C. J. R., Nonino, C. B., & Júnior, C. R. B. (2023) · Research Quarterly for Exercise and Sport · doi:10.1080/02701367.2023.2228388 · Cited by 23
“Training intervention can influence the changes in the content and functionality of the mitochondrial pool (Granata et al., 2018).”
BackgroundExercise—A Panacea of Metabolic Dysregulation in Cancer: Physiological and Molecular Insights
Raun, S. H., Buch‐Larsen, K., Schwarz, P., & Sylow, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073469 · Cited by 20
Concurrent training in team sports: A systematic review
Seipp, D., Quittmann, O. J., Fasold, F., & Klatt, S. (2022) · International Journal of Sports Science & Coaching · doi:10.1177/17479541221099846 · Cited by 24
Mesquita, P. H. C., Godwin, J. S., Ruple, B. A., Sexton, C. L., McIntosh, M. C., Mueller, B. J., Osburn, S. C., Mobley, C. B., Libardi, C. A., Young, K. C., et al. (2023) · The Journal of Physiology · doi:10.1113/jp284822 · Cited by 17
“Several studies have shown increased mitochondrial content and function in response to various forms of ET (Granata et al., 2018; Jacobs et al., 2013; MacInnis & Gibala, 2017).”
BackgroundBotella, J., Perri, E., Caruana, N. J., López-Calcerrada, S., Brischigliaro, M., Jamnick, N. A., Oorschot, V. M. J., Saner, N. J., Díaz‐Lara, J., Taylor, D. F., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66625-8 · Cited by 26
“The mosttime-ef fi cient form of HIIE is termed sprint-interval exercise (SIE) and requires as little as four to six 30-s all-out sprints 23 , making it an attractive exercise prescription given the time constraints of modern society 24,25 .”
Self-citationRønnestad, B. R., Bjerkrheim, K. A., Hansen, J., & Mølmen, K. S. (2022) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2022.948127 · Cited by 19
“There seems to be growing evidence for the importance of accumulated time ≥90% of V̇O2max to maximally stress cardiorespiratory parameters in well-trained endurance athletes (20–22), which also is an intensity domain known to induce a large muscular stimulus eventually leading to favourable muscular adaptations such a…”
BackgroundPreobrazenski, N., Islam, H., & Gurd, B. J. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04669-6 · Cited by 18
Mahatme, S., Vaishali, K., Kumar, N., Rao, V., Kovela, R. K., & Sinha, M. K. (2022) · Medicine and Pharmacy Reports · doi:10.15386/mpr-2201 · Cited by 22
“Training at high-intensity intervals (HIIT) is a time-efficient strategy that significantly induces biogenesis and serves as a potential remodeling technique [3,12-14].”
BackgroundPhysiological adaptations to interval training to promote endurance
Gibala, M. J., Bostad, W., & McCarthy, D. G. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.05.013 · Cited by 23
Jacobs, R. A., & Lundby, C. (2021) · Acta Physiologica · doi:10.1111/apha.13625 · Cited by 18
Barrett, J. S., Whytock, K. L., Strauss, J. A., Wagenmakers, A. J. M., & Shepherd, S. O. (2022) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2021-0631 · Cited by 17
Localized Heat Therapy Improves Mitochondrial Respiratory Capacity but Not Fatty Acid Oxidation
Marchant, E. D., Kaluhiokalani, J. P., Wallace, T. E., Ahmadi, M., Dorff, A., Linde, J. J., Leach, O. K., Hyldahl, R. D., Gifford, J. R., & Hancock, C. R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158500 · Cited by 18
“While mitochondrial content and respiratory capacity often track together, this is not always the case [51].”
BackgroundDelfan, M., Vahed, A., Bishop, D. J., Juybari, R. A., Laher, I., Saeidi, A., Granacher, U., & Zouhal, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.927969 · Cited by 18
Self-citationWesterlund, E., Marelsson, S. E., Karlsson, M., Sjövall, F., Chamkha, I., Frostner, E. Å., Lundgren, J., Fellman, V., Eklund, E. A., Steding‐Ehrenborg, K., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e26745 · Cited by 16
Lee, M. J.-C., Saner, N. J., Ferri, A., García-Domínguez, E., Broatch, J. R., & Bishop, D. J. (2024) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2024.101272 · Cited by 18
Self-citationSpaas, J., Goulding, R. P., Keytsman, C., Fonteyn, L., van Horssen, J., Jaspers, R. T., Eijnde, B. O., & Wüst, R. C. I. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13050 · Cited by 17
Football and team handball training postpone cellular aging in women
Hagman, M., Fristrup, B., Michelin, R., Krustrup, P., & Asghar, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-91255-7 · Cited by 17
“302 Some studies have suggested that VO2max and aerobic capacity are not only limited by 303 cardiorespiratory factors, but also by the mitochondria (32, 36).”
BackgroundA Simple Model for Diagnosis of Maladaptations to Exercise Training
Flockhart, M., Nilsson, L. C., Ekblom, B. T., & Larsen, F. J. (2022) · Sports Medicine - Open · doi:10.1186/s40798-022-00523-x · Cited by 15
“[11] to assess oxidative capacity has previously been validated against mitochondrial respiratory capacity [12], which is related to mitochondrial content and training volume [13].”
BackgroundSzczerbiński, Ł., Taylor, M. A., Puchta, U., Konopka, P., Paszko, A., Citko, A., Szczerbinski, K., Gościk, J., Górska, M., Larsen, S., et al. (2021) · Cells · doi:10.3390/cells10113013 · Cited by 14
“Studies have shown, that although related, these aspects of mitochondrial adaptation may be independent, especially in exercise adaptations [35].”
BackgroundInfluentialSmall peptides: Could they have a big role in metabolism and the response to exercise?
Atakan, M. M., Türkel, İ., Özerkliğ, B., Koşar, Ş. N., Taylor, D. F., Yan, X., & Bishop, D. J. (2024) · The Journal of Physiology · doi:10.1113/jp283214 · Cited by 13
“…adaptations in humans, including elevated abundance of mitochondrial proteins, increased mitochondrial content and greater mitochondrial respiratory function (Daussin et al., 2008; Granata et al., 2016a, b; Montero & Lundby, 2017; for a comprehensive review, please see Granata et al., 2018).”
BackgroundInfluentialSelf-citationEffects of Lactate Administration on Mitochondrial Respiratory Function in Mouse Skeletal Muscle
Takahashi, K., Tamura, Y., Kitaoka, Y., Matsunaga, Y., & Hatta, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.920034 · Cited by 13
Metadata
- Authors
- Granata, C., Jamnick, N. A., & Bishop, D. J.
- Affiliations
- Monash University (AU)
- Victoria University (AU)
- Edith Cowan University (AU)
- Corresponding author
- Granata, Cesare
- Venue
- Sports Medicine
- Published
- 2018-06-22
- Volume
- 48
- Issue
- 8
- Pages
- 1809-1828
- ISSN
- 0112-1642 (ISSN-L)
- 1179-2035
- OpenAlex
- W2809197837
- Cited by
- 247
- References
- 177
- Citations by year
- 2026: 27 · 2025: 37 · 2024: 30 · 2023: 33 · 2022: 34 · 2021: 32 · 2020: 23 · 2019: 25 · 2018: 6
- FWCI
- 5.03
- Type
- journal article
- Language
- en
- Open access
- green
- vuir.vu.edu.au
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Sports Medicine (publishedVersion)
- PubMed (publishedVersion)
- Victoria University Research Repository (Victoria University) (submittedVersion)
- Research Online (Edith Cowan University) (submittedVersion)
- Deakin Research Online (Deakin University) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
- Keywords
- mitochondrial biogenesis, mitochondrial content, mitochondrial respiratory function, endurance training, skeletal muscle, exercise intensity, training volume, mitochondrial translation, sedentary lifestyle, training effects
- MeSH terms
- Adaptation, Physiological, Exercise Test, Humans, Mitochondria, Muscle, Oxygen Consumption, Exercise, Muscle, Skeletal, Cell Respiration, Physical Conditioning, Human
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