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
  • [21] Mas receptor blockade impairs exercise-induced cardiac hypertrophy
    Silva, Christoffer Novais de Farias
    de Bessa, Amanda de Sa Martins
    da Costa, Jaqueline Moura
    Lopes, Paulo Ricardo
    Neves, Angela Ribeiro
    Bombardelli, Monique Machado Louredo Teles
    Colugnati, Diego Basile
    Pedrino, Gustavo Rodrigues
    Mendes, Elizabeth Pereira
    dos Santos, Robson Augusto Sousa
    Biancardi, Manoel Francisco
    dos Santos, Fernanda Cristina Alcantara
    Castro, Carlos Henrique
    PEPTIDES, 2024, 181
  • [22] Interaction of myocardial insulin receptor and IGF receptor signaling in exercise-induced cardiac hypertrophy
    Ikeda, Hiroyuki
    Shiojima, Ichiro
    Ozasa, Yukako
    Yoshida, Masashi
    Holzenberger, Martin
    Kahn, C. Ronald
    Walsh, Kenneth
    Igarashi, Takashi
    Abel, E. Dale
    Komuro, Issei
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2009, 47 (05) : 664 - 675
  • [23] Metabolic Mechanisms of Exercise-Induced Cardiac Remodeling
    Fulghum, Kyle
    Hill, Bradford G.
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2018, 5
  • [24] Bioinformatics Analysis Reveals MicroRNAs Regulating Biological Pathways in Exercise-Induced Cardiac Physiological Hypertrophy
    Xu, Jiahong
    Liu, Yang
    Xie, Yuan
    Zhao, Cuimei
    Wang, Hongbao
    BIOMED RESEARCH INTERNATIONAL, 2017, 2017
  • [25] Exercise-induced cardiac fatigue: the need for speed
    Claessen, Guido
    La Gerche, Andre
    JOURNAL OF PHYSIOLOGY-LONDON, 2016, 594 (11): : 2781 - 2782
  • [26] Exercise-Induced Plasticity in Signaling Pathways Involved in Motor Recovery after Spinal Cord Injury
    Bilchak, Jadwiga N.
    Caron, Guillaume
    Cote, Marie-Pascale
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (09)
  • [27] Intermittent Diet in Exercise-Induced Cardiac Remodeling
    Pacagnelli, Francis Lopes
    Aguiar, Andreo Fernando
    Engel, Leticia Estevam
    Bongiovani, Antonio Claudio
    Gomes, Mariana Janini
    ARQUIVOS BRASILEIROS DE CARDIOLOGIA, 2020, 115 (02) : 194 - 196
  • [28] Quantitative Biology of Exercise-Induced Signal Transduction Pathways
    Liu, Timon Cheng-Yi
    Liu, Gang
    Hu, Shao-Juan
    Zhu, Ling
    Yang, Xiang-Bo
    Zhang, Quan-Guang
    OXYGEN TRANSPORT TO TISSUE XXXIX, 2017, 977 : 419 - 424
  • [29] Computational modeling of apoptotic signaling pathways induced by cisplatin
    Hong, Ji-Young
    Kim, Geun-Hong
    Kim, Jun-Woo
    Kwon, Soon-Sung
    Sato, Eisuke F.
    Cho, Kwang-Hyun
    Shim, Eun Bo
    BMC SYSTEMS BIOLOGY, 2012, 6
  • [30] Endurance Exercise-Induced Cardiac Remodeling: Not All Sports Are Created Equal
    Wasfy, Meagan M.
    Weiner, Rory B.
    Wang, Francis
    Berkstresser, Brant
    Lewis, Gregory D.
    DeLuca, James R.
    Hutter, Adolph M.
    Picard, Michael H.
    Baggish, Aaron L.
    JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 2015, 28 (12) : 1434 - 1440