Exercise-induced signaling pathways to counteracting cardiac apoptotic processes

被引:28
|
作者
Pahlavani, Hamed Alizadeh [1 ]
机构
[1] Farhangian Univ, Dept Phys Educ, Tehran, Iran
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2022年 / 10卷
关键词
exercise; apoptotic; cardiovascular diseases; cardiomyocytes; signaling; signaling pathways; MYOCARDIAL ISCHEMIC TOLERANCE; LEFT-VENTRICULAR HYPERTROPHY; HEAT-SHOCK PROTEINS; PHYSICAL-EXERCISE; MIR-17-3P CONTRIBUTES; ENDURANCE EXERCISE; FOXO TRANSCRIPTION; P38; MAPK; EXPRESSION; ACTIVATION;
D O I
10.3389/fcell.2022.950927
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiovascular diseases are the most common cause of death in the world. One of the major causes of cardiac death is excessive apoptosis. However, multiple pathways through moderate exercise can reduce myocardial apoptosis. After moderate exercise, the expression of anti-apoptotic proteins such as IGF-1, IGF-1R, p-PI3K, p-Akt, ERK-1/2, SIRT3, PGC-1 alpha, and Bcl-2 increases in the heart. While apoptotic proteins such as PTEN, PHLPP-1, GSK-3, JNK, P38MAPK, and FOXO are reduced in the heart. Exercise-induced mechanical stress activates the beta and alpha 5 integrins and subsequently, focal adhesion kinase phosphorylation activates the Akt/mTORC1 and ERK-1/2 pathways, leading to an anti-apoptotic response. One of the reasons for the decrease in exercise-induced apoptosis is the decrease in Fas-ligand protein, Fas-death receptor, TNF-alpha receptor, Fas-associated death domain (FADD), caspase-8, and caspase-3. In addition, after exercise mitochondrial-dependent apoptotic factors such as Bid, t-Bid, Bad, p-Bad, Bak, cytochrome c, and caspase-9 are reduced. These changes lead to a reduction in oxidative damage, a reduction in infarct size, a reduction in cardiac apoptosis, and an increase in myocardial function. After exercising in the heart, the levels of RhoA, ROCK1, Rac1, and ROCK2 decrease, while the levels of PKC epsilon, PKC delta, and PKCalpha are activated to regulate calcium and prevent mPTP perforation. Exercise has an anti-apoptotic effect on heart failure by increasing the PKA-Akt-eNOS and FSTL1-USP10-Notch1 pathways, reducing the negative effects of CaMKII delta, and increasing the calcineurin/NFAT pathway. Exercise plays a protective role in the heart by increasing HSP20, HSP27, HSP40, HSP70, HSP72, and HSP90 along with increasing JAK2 and STAT3 phosphorylation. However, research on exercise and factors such as Pim-1, Notch, and FAK in cardiac apoptosis is scarce, so further research is needed. Future research is recommended to discover more anti-apoptotic pathways. It is also recommended to study the synergistic effect of exercise with gene therapy, dietary supplements, and cell therapy for future research.
引用
收藏
页数:21
相关论文
共 50 条
  • [31] Exercise-induced cardiac troponin elevation: An update on the evidence, mechanism and implications
    Baker, Polly
    Leckie, Todd
    Harrington, Derek
    Richardson, Alan
    IJC HEART & VASCULATURE, 2019, 22 : 181 - 186
  • [32] HBOC Attenuates Intense Exercise-Induced Cardiac Dysfunction
    Li, T.
    Zhu, D.
    Zhou, R.
    Wu, W.
    Li, Q.
    Liu, J.
    INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 2012, 33 (05) : 338 - 345
  • [33] Myokine Musclin Is Critical for Exercise-Induced Cardiac Conditioning
    Harris, Matthew P.
    Zeng, Shemin
    Zhu, Zhiyong
    Lira, Vitor A.
    Yu, Liping
    Hodgson-Zingman, Denice M.
    Zingman, Leonid V.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (07)
  • [34] Energy Metabolism in Exercise-Induced Physiologic Cardiac Hypertrophy
    Xiang, Kefa
    Qin, Zhen
    Zhang, Huimin
    Liu, Xia
    FRONTIERS IN PHARMACOLOGY, 2020, 11
  • [35] Exercise-Induced Cardiac Fatigue in Soldiers Assessed by Echocardiography
    Charton, Marion
    Kervio, Gaeelle
    Matelot, David
    Lachard, Thibault
    Galli, Elena
    Donal, Erwan
    Carre, Francois
    Le Douairon Lahaye, Solene
    Schnell, Frederic
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2021, 8
  • [36] Exercise-induced increases in cardiac troponins and prothrombotic markers
    Koller, A
    MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 2003, 35 (03) : 444 - 448
  • [37] Regulation of mTOR Pathway in Exercise-induced Cardiac Hypertrophy
    Liao, J.
    Li, Y.
    Zeng, F.
    Wu, Y.
    INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 2015, 36 (05) : 343 - 350
  • [38] Phosphoinositide dependent protein kinase 1 is required for exercise-induced cardiac hypertrophy but not the associated mitochondrial adaptations
    Noh, Junghyun
    Wende, Adam R.
    Olsen, Curtis D.
    Kim, Bumjun
    Bevins, Jack
    Zhu, Yi
    Zhang, Quan-Jiang
    Riehle, Christian
    Abel, E. Dale
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2015, 89 : 297 - 305
  • [39] Exercise-induced modulation of cardiac lipid content in healthy lean young men
    Bilet, L.
    van de Weijer, T.
    Hesselink, M. K. C.
    Glatz, J. F. C.
    Lamb, H. J.
    Wildberger, J.
    Kooi, M. E.
    Schrauwen, P.
    Schrauwen-Hinderling, V. B.
    BASIC RESEARCH IN CARDIOLOGY, 2011, 106 (02) : 307 - 315
  • [40] Gene reprogramming in exercise-induced cardiac hypertrophy in swine: A transcriptional genomics approach
    Kuster, Diederik W. D.
    Merkus, Daphne
    Blonden, Lau A.
    Kremer, Andreas
    van Ijcken, Wilfred F. J.
    Verhoeven, Adrie J. M.
    Duncker, Dirk J.
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2014, 77 : 168 - 174