Bečanović, K., Asghar, M., Gadawska, I., Sachdeva, S., Walker, D., Lazarowski, E. R., . . . Leavitt, B. R. (2021). Age-related mitochondrial alterations in brain and skeletal muscle of the YAC128 model of Huntington disease. NPJ aging and mechanisms of disease, 7(1), 26. doi:
https://doi.org/10.1038/s41514-021-00079-2
Chen, X., Ji, Y., Liu, R., Zhu, X., Wang, K., Yang, X., . . . Shen, Y. (2023). Mitochondrial dysfunction: roles in skeletal muscle atrophy. Journal of Translational Medicine, 21(1), 503. doi:
https://doi.org/10.1186/s12967-023-04369-z
Cruz-Jentoft, A. J., & Sayer, A. A. (2019). Sarcopenia. The lancet, 393(10191), 2636-2646. URL:
https://www.thelancet.com/article/S0140-6736(19)31138-9/abstract
Fealy, C. E., Mulya, A., Lai, N., & Kirwan, J. P. (2014). Exercise training decreases activation of the mitochondrial fission protein dynamin-related protein-1 in insulin-resistant human skeletal muscle. Journal of applied physiology, 117(3), 239-245. doi:
https://doi.org/10.1152/japplphysiol.01064.2013
Glancy, B., Hartnell, L. M., Malide, D., Yu, Z.-X., Combs, C. A., Connelly, P. S., . . . Balaban, R. S. (2015). Mitochondrial reticulum for cellular energy distribution in muscle. Nature, 523(7562), 617-620. doi:
https://doi.org/10.1038/nature14614
Gusdon, A. M., Callio, J., Distefano, G., O'Doherty, R. M., Goodpaster, B. H., Coen, P. M., & Chu, C. T. (2017). Exercise increases mitochondrial complex I activity and DRP1 expression in the brains of aged mice. Experimental gerontology, 90, 1-13. doi:
https://doi.org/10.1016/j.exger.2017.01.013
Iqbal, S., & Hood, D. A. (2014). Cytoskeletal regulation of mitochondrial movements in myoblasts. Cytoskeleton, 71(10), 564-572. doi:
https://doi.org/10.1002/cm.21188
Johnson, M. L., Robinson, M. M., & Nair, K. S. (2013). Skeletal muscle aging and the mitochondrion. Trends in Endocrinology & Metabolism, 24(5), 247-256. URL:
https://www.cell.com/trends/endocrinology-metabolism/abstract/S1043-2760(12)00223-8?large_figure=true
Kaczmarek, A., Kaczmarek, M., Ciałowicz, M., Clemente, F. M., Wolański, P., Badicu, G., & Murawska-Ciałowicz, E. (2021). The role of satellite cells in skeletal muscle regeneration—the effect of exercise and age. Biology, 10(10), 1056. doi:
https://doi.org/10.3390/biology10101056
Kamerkar, S. C., Liu, A., & Higgs, H. N. (2025). Mitochondrial fission–changing perspectives for future progress. Journal of cell science, 138(9), jcs263640. doi:
https://doi.org/10.1242/jcs.263640
Kim, H.-J., So, B., Son, J. S., Song, H. S., Oh, S. L., Seong, J. K., . . . Song, W. (2015). Resistance training inhibits the elevation of skeletal muscle derived-BDNF level concomitant with improvement of muscle strength in zucker diabetic rat. Journal of exercise nutrition & biochemistry, 19(4), 281. doi:
https://doi.org/10.5717/jenb.2015.15112402
Larsen, S., Nielsen, J., Hansen, C. N., Nielsen, L. B., Wibrand, F., Stride, N., . . . Dela, F. (2012). Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects. The Journal of physiology, 590(14), 3349-3360. doi:
https://doi.org/10.1113/jphysiol.2012.230185
Li, J., Wang, Z., Li, C., Song, Y., Wang, Y., Bo, H., & Zhang, Y. (2022). Impact of exercise and aging on mitochondrial homeostasis in skeletal muscle: roles of ROS and epigenetics. Cells, 11(13), 2086. doi:
https://doi.org/10.3390/cells11132086
Mahatme, S., Vaishali, K., Kumar, N., Rao, V., Kovela, R. K., & Sinha, M. K. (2022). Impact of high-intensity interval training on cardio-metabolic health outcomes and mitochondrial function in older adults: a review. Medicine and Pharmacy Reports, 95(2), 115. doi:
https://doi.org/10.15386/mpr-2201
Moore, T. M., Zhou, Z., Cohn, W., Norheim, F., Lin, A. J., Kalajian, N., . . . Ho, T. (2019). The impact of exercise on mitochondrial dynamics and the role of Drp1 in exercise performance and training adaptations in skeletal muscle. Molecular Metabolism, 21, 51-67. doi:
https://doi.org/10.1016/j.molmet.2018.11.012
Musci, R. V., Fuqua, J. D., Peelor III, F. F., Nguyen, H. V. M., Richardson, A., Choi, S., . . . Wanagat, J. (2025). Age-induced changes in skeletal muscle mitochondrial DNA synthesis, quantity, and quality in genetically unique rats. Geroscience, 47(1),851-862.doi:
https://doi.org/10.1007/s11357-024-01344-4
Phillips, S. M., Glover, E. I., & Rennie, M. J. (2009). Alterations of protein turnover underlying disuse atrophy in human skeletal muscle. Journal of applied physiology, 107(3), 645-654. doi:
https://doi.org/10.1152/japplphysiol.00452.2009
Preminger, N., & Schuldiner, M. (2024). Beyond fission and fusion—Diving into the mysteries of mitochondrial shape. PLoS Biology, 22(7), e3002671. doi:
https://doi.org/10.1371/journal.pbio.3002671
Qin, X., Li, H., Zhao, H., Fang, L., & Wang, X. (2024). Enhancing healthy aging with small molecules: A mitochondrial perspective. Medicinal research reviews, 44(4), 1904-1922. doi:
https://doi.org/10.1002/med.22034
Radak, Z., Torma, F., Berkes, I., Goto, S., Mimura, T., Posa, A., . . . Higuchi, M. (2019). Exercise effects on physiological function during aging. Free Radical Biology and Medicine, 132, 33-41. doi:
https://doi.org/10.1016/j.freeradbiomed.2018.10.444
Ringholm, S., Gudiksen, A., Frey Halling, J., Qoqaj, A., Meizner Rasmussen, P., Prats, C., . . . Pilegaard, H. (2023). Impact of aging and lifelong exercise training on mitochondrial function and network connectivity in human skeletal muscle. The Journals of Gerontology: Series A, 78(3), 373-383. doi:
https://doi.org/10.1093/gerona/glac164
Sebastián, D., Hernández-Alvarez, M. I., Segalés, J., Sorianello, E., Muñoz, J. P., Sala, D., . . . Gopalacharyulu, P. (2012). Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis. Proceedings of the National Academy of Sciences, 109(14), 5523-5528. doi:
https://doi.org/10.1073/pnas.1108220109
Sheffield-Moore, M., Yeckel, C., Volpi, E., Wolf, S., Morio, B., Chinkes, D., . . . Wolfe, R. (2004). Postexercise protein metabolism in older and younger men following moderate-intensity aerobic exercise. American Journal of Physiology-Endocrinology And Metabolism, 287(3), E513-E522. doi:
https://doi.org/10.1152/ajpendo.00334.2003
Sinha, J. K., Jorwal, K., Singh, K. K., Han, S. S., Bhaskar, R., & Ghosh, S. (2024). The potential of mitochondrial therapeutics in the treatment of oxidative stress and inflammation in aging. Molecular neurobiology, 1-16. doi:
https://doi.org/10.1007/s12035-024-04474-0
Thomas, A. C., Brown, A., Hatt, A. A., Manta, K., Costa‐Parke, A., Kamal, M., . . . Kumbhare, D. (2022). Short‐term aerobic conditioning prior to resistance training augments muscle hypertrophy and satellite cell content in healthy young men and women. The FASEB Journal, 36(9), e22500. doi:
https://doi.org/10.1096/fj.202200398RR
Wilkinson, S. B., Phillips, S. M., Atherton, P. J., Patel, R., Yarasheski, K. E., Tarnopolsky, M. A., & Rennie, M. J. (2008). Differential effects of resistance and endurance exercise in the fed state on signalling molecule phosphorylation and protein synthesis in human muscle. The Journal of physiology, 586(15), 3701-3717. doi:
https://doi.org/10.1113/jphysiol.2008.153916
Yeo, R. X., Dijkstra, P. J., De Carvalho, F. G., Yi, F., Pino, M. F., Smith, S. R., & Sparks, L. M. (2022). Aerobic training increases mitochondrial respiratory capacity in human skeletal muscle stem cells from sedentary individuals. American Journal of Physiology-Cell Physiology. doi:
https://doi.org/10.1152/ajpcell.00146.2022
Zhao, Y.-C., & Gao, B.-h. (2024). Integrative effects of resistance training and endurance training on mitochondrial remodeling in skeletal muscle. European journal of applied physiology, 124(10), 2851-2865. doi:
https://doi.org/10.1007/s00421-024-05549-5
Zhong, Q., Zheng, K., Li, W., An, K., Liu, Y., Xiao, X., . . . An, Z. (2023). Post‐translational regulation of muscle growth, muscle aging and sarcopenia. Journal of cachexia, sarcopenia and muscle, 14(3), 1212-1227. doi:
https://doi.org/10.1002/jcsm.13241