- Seres, I., Paragh, G., Deschene, E., Fulop Jr, T., & Khalil, A. Study of factors influencing the
decreased HDL associated PON1 activity with aging. Experimental gerontology. 2004.39(1),
59-66.
2. Raimundo, N. Mitochondrial pathology: stress signals from the energy factory. Trends in
molecular medicine. 2014. 20(5), 282-292.
3. Li, X., Liu, J., Lu, Q., Ren, D., Sun, X., Rousselle, T., ... & Li, J. AMPK: a therapeutic target
of heart failure—not only metabolism regulation. Bioscience reports. 2019.39(1)
4. Sonjak V, Jacob KJ, Spendiff S, Vuda M, Perez A, Miguez K, et al. Reduced mitochondrial
content, elevated reactive oxygen species, and modulation by denervation in skeletal muscle of prefrail or frail elderly women. The Journals of Gerontology. Series A, Biological
Sciences and Medical Sciences. 2019; 74(12):1887-95. [DOI:10.1093/gerona/glz066]
[PMID]
5. Dominy JE, Puigserver P. Mitochondrial biogenesis through activation of nuclear signaling
proteins. Cold Spring Harbor perspectives in biology. 2013; 5(1-16).
6. Garesse R, Vallejo CG. Animal mitochondrial biogenesis and function: a regulatory crosstalk between two genomes. Gene. 2001; 263(1-2):1-16.
7. Irrcher I, Adhihetty PJ, Sheehan T, Joseph AM, Hood DA. PPARgamma coactivator-1alpha
expression during thyroid hormone- and contractile activity-induced mitochondrial
adaptations. American journal of physiology Cell physiology. 2003;284(6):C1669-77.
8. Wang C, Li Z, Lu Y, Du R, Katiyar S, Yang J, et al. Cyclin D1 repression of nuclear
respiratory factor 1 integrates nuclear DNA synthesis and mitochondrial function.
Proceedings of the National Academy of Sciences of the United States of America.
2006;103(31):11567-72.
9. Hardie DG. AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy.
Nature reviews. Molecular cell biology. 2007; 8(10):774-785.
10. Meirhaeghe A, Crowley V, Lenaghan C, Lelliott C, Green K, Stewart A, et al.
Characterization of the human, mouse and rat PGC1 beta (peroxisome-proliferator-activated
receptor-gamma co-activator 1 beta) gene in vitro and in vivo. The biochemical journal.
2003; 373(Pt 1):155-165.
11. Jornayvaz FR, Shulman GI. Regulation of mitochondrial biogenesis. Essays in biochemistry.
2010; 47:69-84.
12. Islam, H., Hood, D. A., & Gurd, B. J. Looking beyond PGC-1α: emerging regulators of
exercise-induced skeletal muscle mitochondrial biogenesis and their activation by dietary
compounds. Applied Physiology, Nutrition, and Metabolism. 2020. 45(1), 11-23.
13. Valle, I., Álvarez-Barrientos, A., Arza, E., Lamas, S., & Monsalve, M. PGC-1α regulates the
mitochondrial antioxidant defense system in vascular endothelial cells. Cardiovascular
research.2005 .66(3), 562-573.
14. REZAEI, R., NOURSHAHI, M., BIGDELI, M. R., KHODAGHOLI, F., & HAGHPARAST,
A. .Effect of eight weeks continues and HIIT exercises on VEGF-A and VEGFR-2 levels in
stratum, hippocampus and cortex of wistar rat brain,2015.
15. de Cássia Marqueti, R., Almeida, J. A., Nakagaki, W. R., Guzzoni, V., Boghi, F., Renner, A.,
... & Selistre-de-Araújo, H. S. Resistance training minimizes the biomechanical effects of
aging in three different rat tendons. Journal of biomechanics, 2017; 53, 29-35.
16. Rotllan, N., Ramírez, C. M., Aryal, B., Esau, C. C., & Fernández-Hernando, C. Therapeutic
silencing of microRNA-33 inhibits the progression of atherosclerosis in Ldlr−/− mice—brief
report. Arteriosclerosis, thrombosis, and vascular biology. 2013. 33(8), 1973-1977.
17. Liu, H. T., & Pan, S. S. Late exercise preconditioning promotes autophagy against exhaustive
exercise-induced myocardial injury through the activation of the AMPK-mTOR-ULK1
pathway. BioMed Research International, 2019.
18. Ma, S., Wang, Y., Chen, Y., & Cao, F. The role of the autophagy in myocardial
ischemia/reperfusion injury. Biochimica et Biophysica Acta (BBA)-Molecular Basis of
Disease, 2015; 1852(2), 271-276.
19. Jokar, M., Sherafati Moghadam, M., Daryanoosh, F. The effect of a period of high-intensity
interval training on the content of AMPK and PGC-1α proteins in the heart muscle tissue of
rats with type 2 diabetes. Daneshvar Medicine, 29(1), 23-34. doi:
10.22070/daneshmed.2021.12950.0
- 20. Jokar M, Sherafati Moghadam M, Salesi M. THE EFFECT OF ENDURANCE EXERCISE
ON THE CONTENT OF AMPK AND PGC-1Α PROTEINS IN THE LEFT
VENTRICULAR HEART TISSUE OF RATS WITH TYPE 2 DIABETES. Ijdld, 2020; 19
(5) :252-260. URL: http://ijdld.tums.ac.ir/article-1-5941-fa.html
21. Aghaei Bahmanbeglou N, Sherafati Moghadam M, Amirahmadi M. The Effect of Ampk and
P53 Proteins On Tor Pathway Following Endurance Training In The Left Ventricle Of The
Heart Of Diabetic Rats By Streptozotocin And Nicotinamide. ijdld. 2021; 21 (1) :13-23.
URL: http://ijdld.tums.ac.ir/article-1-6016-fa.html
22. Esmailee, B., Abdi, A., Abbassi Daloii, A., & Farzanegi, P. The effect of aerobic exercise
along with resveratrol supplementation on AMPK and MAFbx gene expression of
myocardial diabetic rats. J Birjand Univ Med Sci, 2020; 27(2), 150-60.
23. Moini A, Farsi S, Hoseini S, Mehrzad M. The Effect of Resistance Training on the
Expression of Cardiac Muscle Growth Regulator Messenger Genes in Obese Male Rats.
Armaghane danesh. 2019; 24 (5) :935-949. URL: http://armaghanj.yums.ac.ir/article-1-2570-
fa.html
24. Khalili, A., Nekooeian, A. A., & Khosravi, M. B. (2017). Oleuropein improves glucose
tolerance and lipid profile in rats with simultaneous renovascular hypertension and type 2
diabetes. Journal of Asian natural products research, 19(10), 1011-1021.
25. Horman, S., Beauloye, C., Vanoverschelde, J. L., & Bertrand, L. AMP-activated protein
kinase in the control of cardiac metabolism and remodeling. Current heart failure reports,
2012; 9(3), 164-173.
26. Casuso, R. A., Plaza-Díaz, J., Ruiz-Ojeda, F. J., Aragón-Vela, J., Robles-Sanchez, C.,
Nordsborg, N. B., ... & Huertas, J. R. (). High-intensity high-volume swimming induces more
robust signaling through PGC-1α and AMPK activation than sprint interval swimming in m.
triceps brachii. PLoS One, 2017; 12(10), e0185494.
27. Daniels, A., Van Bilsen, M., Janssen, B. J. A., Brouns, A. E., Cleutjens, J. P. M., Roemen, T.
H. M., ... & Van Nieuwenhoven, F. A. Impaired cardiac functional reserve in type 2 diabetic
db/db mice is associated with metabolic, but not structural, remodelling. Acta physiologica,
2010; 200(1), 11-22.
28. Khalafi, M., Mohebbi, H., Symonds, M. E., Karimi, P., Akbari, A., Tabari, E., ... &
Moghaddami, K. The impact of moderate-intensity continuous or high-intensity interval
training on adipogenesis and browning of subcutaneous adipose tissue in obese male rats.
Nutrients, 2020; 12(4), 925.
29. Sturgeon, K., Muthukumaran, G., Ding, D., Bajulaiye, A., Ferrari, V., & Libonati, J. R.
Moderate‐intensity treadmill exercise training decreases murine cardiomyocyte
cross‐sectional area. Physiological reports, 2015; 3(5), e12406.
30. Onyango, I. G., Lu, J., Rodova, M., Lezi, E., Crafter, A. B., & Swerdlow, R. H. Regulation
of neuron mitochondrial biogenesis and relevance to brain health. Biochimica et Biophysica
Acta (BBA)-Molecular Basis of Disease. 2010.1802(1), 228-234.
31. Chabi, B., Adhihetty, P. J., Ljubicic, V., & Hood, D. A. How is mitochondrial biogenesis
affected in mitochondrial disease?. Medicine & Science in Sports & Exercise, 2005; 37(12),
2102-2110.
32. Baghadam, M., Azizbeidi, K., & Baesi, K. THE EFFECT OF 8 WEEKS AEROBIC
TRAINING ON CARDIAC PGC-1Α AND PLASMA IRISIN IN STZ-INDUCED
DIABETICS’RATS. Iranian Journal of Diabetes and Metabolism. 2019. 18(5), 228-235.
33. Carter, H. N., Pauly, M., Tryon, L. D., & Hood, D. A. Effect of contractile activity on PGC1α transcription in young and aged skeletal muscle. Journal of Applied Physiology. 2018.
124(6), 1605-1615.
- 34. Halling, J. F., Ringholm, S., Olesen, J., Prats, C., & Pilegaard, H. Exercise training protects
against aging-induced mitochondrial fragmentation in mouse skeletal muscle in a PGC-1α
dependent manner. Experimental Gerontology. 2017. 96, 1-6.
35. hadidi, V., Kordi, M., Gaeini, A., hadidi, V., Shafie, A., Hajati modaraie, M. Effect of eight
weeks high intensity interval training on gene expression of PGC-1α, in male healthy rats
fast-slow twitch muscles. Journal of Sport Biosciences, 2015; 7(4): 661-673. doi:
10.22059/jsb.2015.57290
36. Rahimifardin S, Seiahkoheian M, Bolboli L, Farhadi H. The effect of aerobic exercise
training on hypoxia condition through PGC-1α angiogenesis signaling pathway in heart
tissue of male westar rats. Medical Journal of Tabriz University of Medical Sciences. 2020
Jul 18;42(3):263-72.
37. Chavanelle, V., Boisseau, N., Otero, Y. F., Combaret, L., Dardevet, D., Montaurier, C., ... &
Sirvent, P. Effects of high-intensity interval training and moderate-intensity continuous
training on glycaemic control and skeletal muscle mitochondrial function in db/db mice.
Scientific reports, 2017; 7(1), 1-10.
38. Kandi Asadi RH, Arshadi S, Banaei Far AA, Rasouli MH. The effect of 12-week aerobic
trainings on mitochondrial biogenesis indicators in skeletal muscle among male rats. Medical
Journal of Tabriz University of Medical Sciences & Health Services. 2020 Aug 1;42(3).
39. Taghibeikzadehbadr, P., shabkhiz, F., shahrbanian, S. Expression of PGC-1 alpha isoforms in
response to eccentric and concentric resistance training in healthy subjects. Journal of Sport
Biosciences, 2020; 11(4): 447-462. doi: 10.22059/jsb.2019.287895.1360
40. Damirchi, A., & Ebadi, B. (2019). The effects of the intensity of interval training on
mitochondrial dynamics-related proteins in the heart of male rats with myocardial infarction.
Journal of Applied Exercise Physiology, 14(28), 159-172.
41. Baghdam, Mohammad, Mohammadzadeh Salamat, Khalid, Azizbeigi, Kamal, Bahazi,
Kazem. The effect of resistance training on irzin and expression of PGC1α gene in the heart
muscle of STZ diabetic rats. Community health,1397 ; 12(3): 58-64. doi:
10.22123/chj.2019.130374.1139
42. Shabani, M., Choobineh, S., Kordi, M. R., & Afghan, M. The Effect of 8 Weeks of High
Intensity Interval Training on the Expression of PGC-1α and VEGF Genes in Myocardial
Muscle of Male Healthy Rats. Journal of Sport Biosciences, 2016; 8(2), 169-176.
43. Millay, D. P., & Olson, E. N. Making muscle or mitochondria by selective splicing of PGC1α. Cell metabolism, 2013; 17(1), 3-4.
44. Kang, C., & Ji, L. L. Role of PGC-1α signaling in skeletal muscle health and disease. Annals
of the New York Academy of Sciences, 2012; 1271(1), 110.
45. Lowell, B. B., & Shulman, G. I. Mitochondrial dysfunction and type 2 diabetes. Science,
2005; 307(5708), 384-387.
46. Ventura-Clapier, R., Garnier, A., & Veksler, V. Transcriptional control of mitochondrial
biogenesis: the central role of PGC-1α. Cardiovascular research, 2008; 79(2), 208-217.
47. Berg JM T, Stryer L translated by Mohammadi R. Biochemistry. Aeizh. 2012.
48. Lee, H., Kim, K., Kim, B., Shin, J., Rajan, S., Wu, J., ... & Park, J. Y. A cellular mechanism
of muscle memory facilitates mitochondrial remodelling following resistance training. The
Journal of physiology, 2018; 596(18), 4413-4426.
49. Wibom , R., Hultman, E., Johansson, M., Matherei, K., Constantin-Teodosiu, D., & Schantz,
P. G. Adaptation of mitochondrial ATP production in human skeletal muscle to endurance
training and detraining. Journal of Applied Physiology, 1992; 73(5), 2004-2010.
- 50. Hamidie, R. D. R., Yamada, T., Ishizawa, R., Saito, Y., & Masuda, K. Curcumin treatment
enhances the effect of exercise on mitochondrial biogenesis in skeletal muscle by increasing
cAMP levels. Metabolism, 2015; 64(10), 1334-1347.
51. Kang, C., & Ji, L. L. Role of PGC-1α signaling in skeletal muscle health and disease. Annals
of the New York Academy of Sciences, 2012; 1271(1), 110.
52. Wang, C., Li, Z., Lu, Y., Du, R., Katiyar, S., Yang, J., ... & Pestell, R. G. Cyclin D1
repression of nuclear respiratory factor 1 integrates nuclear DNA synthesis and
mitochondrial function. Proceedings of the National Academy of Sciences, 2006; 103(31),
11567-11572.
53. Theilen NT, Kunkel GH, Tyagi SC. The role of exercise and TFAM in preventing skeletal
muscle atrophy. Journal of Cellular Physiology. 2017; 232(9):2348-58.
[DOI:10.1002/jcp.25737] [PMID] [PMCID]
54. Ahmadi F, Siahkouhian M, Mirdar S, Tapak L. The Effect of a Detraining After Resistance
Training on the Histochemical Expression of Potassium Channels and Mitochondrial
Biogenesis of Heart Tissue in Male Rats. Horizon Med Sci. 2021; 27 (2) :230-245. URL:
http://hms.gmu.ac.ir/article-1-3501-fa.html
55. Bakhtiyari, A., Gaeni, A., Choobineh, S., Kordi, M., Hedayati, M. The Comparison of the
Influence of 12-Week High- Intensity Interval Training and Continuous Moderate Intensity
Training on PGC-1α and Tfam Mitochondrial Proteins Expressions in Gastrocnemius Muscle
of Elderly Rats. Journal of Animal Biology, 2019; 11(4): 11-20.
56. Sharafi Dehrhm, F., Soori, R., Rastegar MM, M., & Sadegh, A. The effect of high intensity
interval training on muscular biomarkers of mitochondrial biogenesis in male rats. Journal of
Babol University of Medical Sciences, 2017; 19(6), 57-63.
57. Gahramani M, Karbalaeifar S. Effect of eight weeks high intensity interval training on NRF1, 2 and Tfam gene expressione levels in ST muscles in rats with myocardial infarction.
Medical Journal of Tabriz University of Medical Sciences. 2019 Dec 19;41(6):75-82.
58. Tabari, E., Mohebbi, H. The effects of high and moderate intensity interval training on
skeletal muscle of TFAM and NRF1 in type2 diabetic male rats. Journal of Practical Studies
of Biosciences in Sport, 2021; (): -. doi: 10.22077/jpsbs.2020.3640.1579
59. Granata, C., Oliveira, R. S., Little, J. P., Renner, K., & Bishop, D. J. Mitochondrial
adaptations to high‐volume exercise training are rapidly reversed after a reduction in training
volume in human skeletal muscle. The FASEB journal, 2016; 30(10), 3413-3423.
O'Hagan, K. A., Cocchiglia, S., Zhdanov, A. V., Tambuwala, M. M., Cummins, E. P.,
Monfared, M., ... & Allan, B. B. PGC-1α is coupled to HIF-1α-dependent gene expression
by increasing mitochondrial oxygen consumption in skeletal muscle cells. Proceedings of
the National Academy of Sciences, 2009; 106(7), 2188-2193.
|
