Preview

Экстремальная биомедицина

Расширенный поиск

Влияние физических нагрузок на эпигенетические модификации генома: значение для спортивной медицины (обзор)

https://doi.org/10.47183/mes.2026-467

Аннотация

Введение. Физическая нагрузка является одним из наиболее мощных средовых факторов, модулирующих эпигенетические модификации генома. Регуляция активности генов посредством химической модификации ДНК, изменения гистонов и некодирующих РНК выступает связующим звеном между тренировками и формирующимся фенотипом спортсмена. Данные литературы остаются разрозненными и нередко противоречивыми, что обусловлено методологическими сложностями, гетерогенностью исследуемых групп и отсутствием стандартизации протоколов.

Цель. Систематизация и обобщение современных данных о влиянии физических нагрузок на эпигенетические модификации генома, анализ их вклада в процессы адаптации, восстановления и формирования риска патологических состояний у спортсменов, а также оценка перспектив применения эпигенетических маркеров в спортивной медицине.

Обсуждение. Физические упражнения индуцируют специфические изменения в трех основных звеньях эпигенома. Острые и хронические нагрузки вызывают гипометилирование промоторов генов энергетического обмена (PPARGC1A, PDK4, PPARD), что сопровождается усилением экспрессии и митохондриальным биогенезом. Модификации гистонов (ацетилирование, фосфорилирование H3.3-Ser-31, лактилирование) изменяют плотность упаковки хроматина. Спектр микроРНК зависит от типа и продолжительности тренировок, однако информация по отдельным микроРНК (в том числе miR-1) остается противоречивой, что в значительной степени определяется различиями в методологии (тренированность участников, временные точки, способ нормализации, пол). Сигнальные каскады (AMPK, MAPK, IGF-1/Akt, NF-κB, NFE2L2) интегрируют энергетические сигналы и эпигенетический ответ. Эпигенетический ответ тканеспецифичен и модулируется полом, возрастом и этнической принадлежностью. Отдельными перспективными направлениями являются анализ экзеркинов, в том числе микроРНК внеклеточных везикул (EVs), и нутриэпигенетика.

Выводы. Физические нагрузки закономерно вызывают характерные эпигенетические модификации, которые участвуют в адаптации, и могут рассматриваться как потенциальные биомаркеры функционального состояния спортсмена. Перспективные направления применения в спортивной медицине включают мониторинг восстановления через эпигенетические часы, прогноз травматизма и перетренированности, персонализацию тренировок и расширение «Athlete Biological Passport» (биологического «паспорта» спортсмена) за счет эпигенетических маркеров. Внедрение результатов в клиническую практику требует преодоления методологических ограничений и дальнейших проспективных исследований.

Об авторах

А. И. Кадыкова
Национальный центр спортивной медицины Федерального медико-биологического агентства
Россия

Кадыкова Анастасия Игоревна

Москва



Е. Д. Копылов
Национальный центр спортивной медицины Федерального медико-биологического агентства
Россия

Копылов Евгений Дмитриевич

Москва



Н. С. Гладышев
Национальный центр спортивной медицины Федерального медико-биологического агентства
Россия

Гладышев Никита Сергеевич

Москва



Р. В. Деев
Национальный центр спортивной медицины Федерального медико-биологического агентства
Россия

Деев Роман Вадимович, канд. мед. наук, доцент

Москва



А. В. Жолинский
Национальный центр спортивной медицины Федерального медико-биологического агентства
Россия

Жолинский Андрей Владимирович, канд. мед. наук

Москва



Список литературы

1. Widmann M, Nieß AM, Munz B. Physical exercise and epigenetic modifications in skeletal muscle. Sports Medicine. 2019;49(4):509–23. https://doi.org/10.1007/s40279-019-01070-4

2. Plaza-Diaz J, Izquierdo D, Torres-Martos Á, Tariq Baig A, Aguillera CM, Ruiz-Ojeda FJ. Impact of physical activity and exercise on the epigenome in skeletal muscle and effects on systemic metabolism. Biomedicines. 2022;10(1):126. https://doi.org/10.3390/biomedicines10010126

3. Geiger C, Needhamsen M, Emanuelsson EB, Norrbom J, Steindorf K, Sundberg CJ, et al. DNA methylation of exercise-responsive genes differs between trained and untrained men. BMC Biology. 2024;22(1):147. https://doi.org/10.1186/s12915-024-01938-6

4. Seaborne RA, Strauss J, Cocks M, Shepherd S, O’Brien TD, van Someren KA, et al. Methylome of human skeletal muscle after acute & chronic resistance exercise training, detraining & retraining. Scientific Data. 2018;5:180213. https://doi.org/10.1038/sdata.2018.213

5. Jacques M, Hiam D, Craig J, Barrès R, Eynon N, Voisin S. Epigenetic changes in healthy human skeletal muscle following exercise — a systematic review. Epigenetics. 2019;14(7):633–48. https://doi.org/10.1080/15592294.2019.1614416

6. Максименко ЛВ. Эпигенетика как доказательная база влияния образа жизни на здоровье и болезни. Профилактическая медицина. 2019;22(2):115–20. https://doi.org/10.17116/profmed201922021115

7. Zhang M, Hu T, Ma T, Huang W, Wang Y. Epigenetics and environmental health. Frontiers in Medicine. 2024;18(4):571–96. https://doi.org/10.1007/s11684-023-1038-2

8. Voisin S, Seale K, Jacques M, Landen S, Harvey NR, Haupt LM, et al. Exercise is associated with younger methylome and transcriptome profiles in human skeletal muscle. Aging Cell. 2024;23(1):e13859. https://doi.org/10.1111/acel.13859

9. Zheng X, Liu X, Guo Y, Lv Y, Lin C, Wang D, et al. Physical exercise and epigenetic modifications in skeletal muscle, brain, and heart. Epigenetics Chromatin. 2025;18(1):12. https://doi.org/10.1186/s13072-025-00576-8

10. Жолинский АВ, Гришина ЖВ, Кадыкова АИ, Макарова ГА, Деев РВ. Подходы к классификации спортивных дисциплин с учетом их влияния на биохимический профиль спортсмена. Спортивная медицина: наука и практика. 2022;12(2):82–95. https://doi.org/10.47529/2223-2524.2022.2.7

11. Grazioli E, Dimauro I, Mercatelli N, Wang G, Pitsiladis Y, Di Luigi L, et al. Physical activity in the prevention of human diseases: role of epigenetic modifications. BMC Genomics. 2017;18(8):802. https://doi.org/10.1186/s12864-017-4193-5

12. Fernández Pérez R, Lecumberri-Arteta J, Kulis M, Botta-Orfila T, Rodriguez-Vilarrupla A, Yanguas X, et al. Epigenetic signatures, age acceleration, and injury risk in elite female and male soccer players. Scientific Reports. 2025;15:41826. https://doi.org/10.1038/s41598-025-25784-w

13. Farsetti A, Illi B, Gaetano C. How epigenetics impacts on human diseases. European Journal of Internal Medicine. 2023;114:15–22. https://doi.org/10.1016/j.ejim.2023.05.036

14. Brooke RT, Kocher T, Zauner R, Gordevicius J, Milciute M, Nowakowski M, et al. Epigenetic age monitoring in professional soccer players for tracking recovery and the effects of strenuous exercise. Aging Cell. 2025;24:e70182. https://doi.org/10.1111/acel.70182

15. Ding H, Deng Q, Guo Z. Genetic and epigenetic determinants of injury risk and recovery in elite athletes: toward precision sports medicine. Gene. 2026;980:149957. https://doi.org/10.1016/j.gene.2025.149957

16. Mavromatis LA, Rosoff DB, Bell AS, Jung J, Wagner J, Lohoff FW. Multi-omic underpinnings of epigenetic aging and human longevity. Nature Communications. 2023;14(1):2236. https://doi.org/10.1038/s41467-023-37729-w

17. Mallett G. The effect of exercise and physical activity on skeletal muscle epigenetics and metabolic adaptations. European Journal of Applied Physiology. 2025;125(3):611–27. https://doi.org/10.1007/s00421-025-05704-6

18. Semenova EA, Hall ECR, Ahmetov II. Genes and athletic performance: The 2023 Update. Genes. 2023;14(6):1235. https://doi.org/10.3390/genes14061235

19. Астратенкова ИВ, Ахметов ИИ, Гольберг НД, Рогозкин ВА. Регуляция метаболизма скелетных мышц эпигенетическими факторами. Российский физиологический журнал им. И.М. Сеченова. 2019;105(9):1113–21. https://doi.org/10.1134/S0869813919090036

20. Зайцева АО, Аксенов МО. Экспрессия генов как индикатор долговременной адаптации к физическим нагрузкам. Физическая культура и студенческий спорт. 2022;1(2):183–8. https://doi.org/10.18500/2782-4594-2022-1-2-183-188

21. Marrouh A, El Haddouchi A, Kartti S, El Fahime E, Boutayeb S, Chagar Y, et al. The role of genetic and epigenetic factors in sports-related muscle, bone, and brain injuries. Science Progress. 2025;108(4). https://doi.org/10.1177/00368504251385937

22. Ostaiza-Cardenas J, Tobar AC, Costa SC, Calero DS, Lopez-Carrera A, Bermundez FG, et al. Epigenetic modulation by life-style: advances in diet, exercise, and mindfulness for disease prevention and health optimization. Frontiers in Nutrition. 2025;12:1632999. https://doi.org/10.3389/fnut.2025.1632999

23. Etayo-Urtasun P, Sáez de Asteasu ML, Izquierdo M. Effects of exercise on DNA methylation: A systematic review of randomized controlled trials. Sports Medicine. 2024;54(8):2059–69. https://doi.org/10.1007/s40279-024-02033-0

24. Каплун ДС, Калюжный ДН, Прохорчук ЕБ, Женило СВ. Метилирование ДНК: распределение в геноме, механизм регуляции и мишень для терапии. ActaNaturae. 2022;14(4):4–19. https://doi.org/10.32607/actanaturae.11822

25. Barrès R, Yan J, Egan B, Treebak JT, Rasmussen M, Fritz T, et al. Acute exercise remodels promoter methylation in human skeletal muscle. Cell Metabolism. 2012;15(3):405–11. https://doi.org/10.1016/j.cmet.2012.01.001

26. Seaborne RA, Strauss J, Cocks M, Shepherd S, O’Brien TD, van Someren K, et al. Human skeletal muscle possesses an epigenetic memory of hypertrophy. Scientific Reports. 2018;8(1):1898. https://doi.org/10.1038/s41598-018-20287-3

27. Doenecke D, Albig W, Bode C, Drabent B, Franke K, Gavenis K, et al. Histones: genetic diversity and tissue-specific gene expression. Histochemistry and Cell Biology. 1997;107(1):1–10. https://doi.org/10.1007/s004180050083

28. Chen HP, Zhao YT, Zhao TC. Histone deacetylases and mechanisms of regulation of gene expression. Critical Reviews in Oncology. 2015;20(1–2):35–47. https://doi.org/10.1615/critrevoncog.2015012997

29. Jeppesen J, Kiens B. Regulation and limitations to fatty acid oxidation during exercise. The Journal of Physiology. 2012;590(5):1059–68. https://doi.org/10.1113/jphysiol.2011.225011

30. Chen M, Zhang C, Tian P, Tan Q, Wei Y, Wang Z, et al. Epigenetic reader ZMYND11 noncanonical function restricts HNRNPA1-mediated stress granule formation and oncogenic activity. Signal Transduction and Targeted Therapy. 2024;9(1):256. https://doi.org/10.1038/s41392-024-01961-7

31. Maruyama S, Kawano F. Phosphorylation-mimicking histone H3.3 rescues exercise-induced gene responses in an epigenetic aging model of mouse skeletal muscle. Laboratory Animal Research. 2025;41(1):25. https://doi.org/10.1186/s42826-025-00254-6

32. Zhang D, Tang Z, Huang H, Zhou G, Cui C, Weng Y, et al. Metabolic regulation of gene expression by histone lactylation. Nature. 2019;574(7779):575–80. https://doi.org/10.1038/s41586-019-1678-1

33. Yu X, Yang J, Xu J, Pan H, Wang W, Yu X, et al. Histone lactylation: from tumor lactate metabolism to epigenetic regulation. International Journal of Biological Sciences. 2024;20(5):1833–54. https://doi.org/10.7150/ijbs.91492

34. Grieb A, Schmitt A, Fragasso A, Widmann M, Maturana FM, Burgstahler C, et al. Skeletal muscle microRNA patterns in response to a single bout of exercise in females: biomarkers for subsequent training adaptation? Biomolecules. 2023;13(6):884. https://doi.org/10.3390/biom13060884

35. Nielsen S, Scheele C, Yfanti C, Akerstrom T, Nielsen AR, Pedersen BK, et al. Muscle specific microRNAs are regulated by endurance exercise in human skeletal muscle. The Journal of Physiology. 2010;588(20):4029–37. https://doi.org/10.1113/jphysiol.2010.189860

36. Russell AP, Lamon S, Boon H, Wada S, Guller I, Brown EL, et al. Regulation of miRNAs in human skeletal muscle following acute endurance exercise and short-term endurance training. The Journal of Physiology. 2013;591(18):4637–53. https://doi.org/10.1113/jphysiol.2013.255695

37. Baggish AL, Hale A, Weiner RB, Lewis GD, Systrom D, Wang F, et al. Dynamic regulation of circulating microRNA during acute exhaustive exercise and sustained aerobic exercise training. The Journal of Physiology. 2011;589(Pt 16):3983–94. https://doi.org/10.1113/jphysiol.2011.213363

38. Gomes CP, Oliveira GP, Madrid B, Almeida JA, Franco OL, Pereira RW. Circulating miR-1, miR-133a, and miR-206 levels are increased after a half-marathon run. Biomarkers. 2014;19(7):585–9. https://doi.org/10.3109/1354750X.2014.952663

39. Sieland J, Niederer D, Engeroff T, Vogt L, Troidl C, Schmitz-Rixen T, et al. Effects of single bouts of different endurance exercises with different intensities on microRNA biomarkers with and without blood flow restriction: a three-arm, randomized crossover trial. European Journal of Applied Physiology. 2021;121(11):3019–36. https://doi.org/10.1007/s00421-021-04786-2

40. Telles GD, Libardi CA, Conceicao MS, Vechin FC, Lixandrao ME, de Andrade ALL, et al. Time course of skeletal muscle miRNA expression after resistance, high-intensity interval, and concurrent exercise. Medicine and Science in Sports and Exercise. 2021;53(7):1442–53. https://doi.org/10.1249/MSS.0000000000002603

41. Faraldi M, Gomarasca M, Sansoni V, Perego S, Banfi G, Lombardi G. Normalization strategies differently affect circulating miRNA profile associated with the training status. Scientific Reports. 2019;9(1):1584. https://doi.org/10.1038/s41598-019-38505-x

42. Shiotsu H, Okada K, Shibuta T, Kobayashi Y, Shirahama S, Kuroki C, et al. The influence of pre-analytical factors on the analysis of circulating microRNA. MicroRNA. 2018;7(3):195–203. https://doi.org/10.2174/2211536607666180709143335

43. Welsh JA, Goberdhan DCI, O’Driscoll L, Buzas EI, Blenkiron C, Bussolati B, et al. Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches. Journal of Extracellular Vesicles. 2024;13(2):e12404. https://doi.org/10.1002/jev2.12404

44. Habibi P, Alihemmati A, Ahmadiasl N, Fateh A, Anvari E. Exercise training attenuates diabetes-induced cardiac injury through increasing miR-133a and improving pro-apoptosis/ anti-apoptosis balance in ovariectomized rats. Iranian Journal of Basic Medical Sciences. 2020;23(1):79–85. https://doi.org/10.22038/IJBMS.2019.36731.8750

45. Horak M, Zlamal F, Iliev R, Kucera J, Cacek J, Svobodova L, et al. Exercise-induced circulating microRNA changes in athletes in various training scenarios. PLoS One. 2018;13(1):e0191060. https://doi.org/10.1371/journal.pone.0191060

46. Zhao J, Song Y, Zeng Y, Chen L, Yan F, Chen A, et al. Improvement of hyperlipidemia by aerobic exercise in mice through a regulatory effect of miR-21a-5p on its target genes. Scientific Reports. 2021;11(1):11966. https://doi.org/10.1038/s41598-021-91583-8

47. Stoica VC, Diculescu MM, Mănuc M, Constantinescu I, Gardan IP, Gardan AD. The role of miRNAs and epigenetic factors in non-alcoholic fatty liver disease — a systematic review. Current Health Sciences Journal. 2025;51(1):37–52. https://doi.org/10.12865/CHSJ.51.01.04

48. Xu T, Zhou Q, Che L, Das S, Wang L, Jiang J, et al. Circulating miR-21, miR-378, and miR-940 increase in response to an acute exhaustive exercise in chronic heart failure patients. Oncotarget. 2016;7(11):12414–25. https://doi.org/10.18632/oncotarget.6966

49. Wang L, Feng J, Feng X, Meng D, Zhao X, Wang J, et al. Exercise-induced circular RNA circUtrn is required for cardiac physiological hypertrophy and prevents myocardial ischaemia-reperfusion injury. Cardiovascular Research. 2023;119(16):2638–52. https://doi.org/10.1093/cvr/cvad161

50. Ferraro E, Giammarioli AM, Chiandotto S, Spoletini I, Rosano G. Exercise-induced skeletal muscle remodeling and metabolic adaptation: redox signaling and role of autophagy. Antioxidants & Redox Signaling. 2014;21(1):154–76. https://doi.org/10.1089/ars.2013.5773

51. McGee SL, Hargreaves M. AMPK-mediated regulation of transcription in skeletal muscle. Clinical Science. 2010;118(8):507–18. https://doi.org/10.1042/CS20090533

52. Hoffman NJ, Parker BL, Chaudhuri R, Fisher-Wellman KH, Kleinert M, Humphrey SJ, et al. Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates. Cell Metabolism. 2015;22(5):922–35. https://doi.org/10.1016/j.cmet.2015.09.001

53. Li Q, Liu Q, Lin Z, Lin W, Huang F, Zhu P. Hypomethylation in promoters of PGC-1α involved in exercise-driven skeletal muscular alterations in old age. Open Life Sciences. 2024;19(1):20220959. https://doi.org/10.1515/biol-2022-0959

54. Kong S, Cai B, Nie Q. PGC-1α affects skeletal muscle and adipose tissue development by regulating mitochondrial biogenesis. Molecular Genetics and Genomics. 2022;297(3):621–33. https://doi.org/10.1007/s00438-022-01878-2

55. Yoshida T, Delafontaine P. Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy. Cells. 2020;9(9):1970. https://doi.org/10.3390/cells9091970

56. Ilyushchenko AK, Matchekhina LV, Melnitskaia AA, Strazhesko ID. Associations of IGF-1 and IGFBP-3 with aging and the development of age-associated diseases. Advances in Gerontology. 2024;14(3):118–26. https://doi.org/10.1134/S2079057025600041

57. da Silva Rodrigues G, Noma IHY, Noronha NY, Watanabe LM, da Silva Sobrinho AC, de Lima JGR, et al. Eight weeks of physical training decreases 2 years of DNA methylation age of sedentary women. Research Quarterly for Exercise and Sport. 2024;95(2):405–15. https://doi.org/10.1080/02701367.2023.2228388

58. Yin L, Cai WJ, Chang XY, Li J, Zhu LY, Su XH, et al. Analysis of PTEN expression and promoter methylation in Uyghur patients with mild type 2 diabetes mellitus. Medicine. 2018;97(49):e13513. https://doi.org/10.1097/MD.0000000000013513

59. Scheffer DDL, Latini A. Exercise-induced immune system response: Anti-inflammatory status on peripheral and central organs. Biochimica et Biophysica Acta — Molecular Basis of Disease. 2020;1866(10):165823. https://doi.org/10.1016/j.bbadis.2020.165823

60. Tarnowski M, Kopytko P, Piotrowska K. Epigenetic Regulation of Inflammatory Responses in the Context of Physical Activity. Genes. 2021;12(9):1313. https://doi.org/10.3390/genes12091313

61. Malkowska P, Sawczuk M. Cytokines as biomarkers for evaluating physical exercise in trained and non-trained individuals: A narrative review. International Journal of Molecular Sciences. 2023;24(13):11156. https://doi.org/10.3390/ijms241311156

62. Vargas-Mendoza N, Morales-González Á, Madrigal-Santillán EO, Madrigal-Bujaidar E, Alvarez-Gonzalez I, Garcia-Melo LF, et al. Antioxidant and adaptative response mediated by Nrf2 during physical exercise. Antioxidants. 2019;8(6):196. https://doi.org/10.3390/antiox8060196

63. Rönn T, Volkov P, Davegårdh C, Dayeh T, Hall E, Olsson AH, et al. A six months exercise intervention influences the genome-wide DNA methylation pattern in human adipose tissue. PLoS Genetics. 2013;9(6):e1003572. https://doi.org/10.1371/journal.pgen.1003572

64. Denham J, O’Brien BJ, Marques FZ, Charchar FJ. Changes in the leukocyte methylome and its effect on cardiovascular-related genes after exercise. Journal of Applied Physiology. 2015;118(4):475–88. https://doi.org/10.1152/japplphysiol.00878.2014

65. Kawamura T, Higuchi M, Radak Z, Taki Y. Exercise as a geroprotector: focusing on epigenetic aging. Aging. 2025;17(6):1–14. https://doi.org/10.18632/aging.206278

66. Maasar MF, Turner DC, Gorski PP, Seaborne RA, Strauss JA, Shepherd SO, et al. The comparative methylome and transcriptome after change of direction compared to straight line running exercise in human skeletal muscle. Frontiers in Physiology. 2021;12:619447. https://doi.org/10.3389/fphys.2021.619447

67. D’Souza RF, Bjørnsen T, Zeng N, Aasen KMM, Raastad T, Cameron-Smith D, et al. MicroRNAs in muscle: Characterizing the powerlifter phenotype. Frontiers in Physiology. 2017;8:383. https://doi.org/10.3389/fphys.2017.00383

68. da Silva Rodrigues G, Noronha NY, Noma IHY, de Lima JGR, da Silva Sobrinho AC, de Souza Pinhel MA, et al. 14-Week exercise training modifies the DNA methylation levels at gene sites in non-Alzheimer’s disease women aged 50 to 70 years. Experimental Gerontology. 2024;186:112362. https://doi.org/10.1016/j.exger.2024.112362

69. Oxfeldt M, Dalgaard LB, Jørgensen EB, Johansen FT, Dalgaard EB, Ortenblad N, et al. Molecular markers of skeletal muscle hypertrophy following 10 wk of resistance training in oral contraceptive users and nonusers. Journal of Applied Physiology. 2020;129(6):1355–64. https://doi.org/10.1152/japplphysiol.00562.2020

70. Whitham M, Parker BL, Friedrichsen M, Hingst JR, Hjort M, Hughes WE, et al. Extracellular vesicles provide a means for tissue crosstalk during exercise. Cell Metabolism. 2018;27(1):237–51.e4. https://doi.org/10.1016/j.cmet.2017.12.001

71. Frühbeis C, Helmig S, Tug S, Simon P, Krämer-Albers EM. Physical exercise induces rapid release of small extracellular vesicles into the circulation. Journal of Extracellular Vesicles. 2015;4:28239. https://doi.org/10.3402/jev.v4.28239

72. Lisi V, Senesi G, Bertola N, Pecoraro M, Bolis S, Gualerzi A, et al. Plasma-derived extracellular vesicles released after endurance exercise exert cardioprotective activity through the activation of antioxidant pathways. Redox Biology. 2023;63:102737. https://doi.org/10.1016/j.redox.2023.102737

73. Kargl CK, Sterczala AJ, Santucci D, Congkright WR, Krajewski KT, Martin BJ, et al. Circulating extracellular vesicle characteristics differ between men and women following 12 weeks of concurrent exercise training. Physiological Reports. 2024;12(9):e16016. https://doi.org/10.14814/phy2.16016

74. Fliflet AM, Tan Y, Barnes TM, Vijayan AN, Choi SJ, Deutz MT, et al. Human plasma extracellular vesicles as an exercise mimetic to preserve skeletal muscle plasticity during disuse. NPJ Microgravity. 2026. https://doi.org/10.1038/s41526-026-00582-4

75. Silver JL, Alexander SE, Dillon HT, Lamon S, Wadley GD. Extracellular vesicular miRNA expression is not a proxy for skeletal muscle miRNA expression in males and females following acute, moderate intensity exercise. Physiological Reports. 2020;8(14):e14520. https://doi.org/10.14814/phy2.14520

76. Williams A, Wadsworth DD, Geetha T. Exercise, epigenetics, and body composition: molecular connections. Cells. 2025;14(19):1553. https://doi.org/10.3390/cells14191553

77. Dragčević D, Perinović Jozić H, Jozić T, Galić S. Athlete biological passport: longitudinal biomarkers and statistics in the fight against doping. Archives of Industrial Hygiene and Toxicology. 2024;75(1):24–31. https://doi.org/10.2478/aiht-2024-75-3793

78. Sessa F, Salerno M, Di Mizio G, Bertozzi G, Messina G, Tomaiuolo B, et al. Anabolic androgenic steroids: searching new molecular biomarkers. Frontiers in Pharmacology. 2018;9:1321. https://doi.org/10.3389/fphar.2018.01321

79. Durussel J, Haile DW, Mooses K, Daskalaki E, Beattie W, Mooses M, et al. Blood transcriptional signature of recombinant human erythropoietin administration and implications for antidoping strategies. Physiological Genomics. 2016;48(3):202–9. https://doi.org/10.1152/physiolgenomics.00108.2015

80. Wilkin T, Hamilton NA, Cawley AT, Bhat S, Baoutina A. Towards a robust test to detect gene doping for anabolic enhancement in human athletes. International Journal of Molecular Sciences. 2024;25(5):2570. https://doi.org/10.3390/ijms25052570


Дополнительные файлы

1. Глоссарий ключевых генов и микроРНК
Тема
Тип Исследовательские инструменты
Скачать (920KB)    
Метаданные ▾

Рецензия

Для цитирования:


Кадыкова А.И., Копылов Е.Д., Гладышев Н.С., Деев Р.В., Жолинский А.В. Влияние физических нагрузок на эпигенетические модификации генома: значение для спортивной медицины (обзор). Экстремальная биомедицина. https://doi.org/10.47183/mes.2026-467

For citation:


Kadykova A.I., Kopylov E.D., Gladyshev N.S., Deev R.V., Zholinsky A.V. Influence of physical exercise on epigenetic modifications of the genome: significance for sports medicine (a review). Extreme Medicine. (In Russ.) https://doi.org/10.47183/mes.2026-467

Просмотров: 56

JATS XML


Creative Commons License
Контент доступен под лицензией Creative Commons Attribution 4.0 License.


ISSN 3033-8964 (Print)
ISSN 3033-8972 (Online)