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Published on: June 3, 2018
Exercise-induced signaling pathways to counteracting cardiac apoptotic processes
1Department of Physical Education, Farhangian University, Tehran, Iran.
Insights
Moderate exercise reduces cardiac apoptosis by increasing anti-apoptotic proteins and decreasing pro-apoptotic factors. This cardioprotective effect enhances myocardial function and reduces infarct size, highlighting exercise
Area of Science:
- Cardiology
- Exercise Physiology
- Molecular Biology
Background:
- Cardiovascular diseases are the leading global cause of death.
- Excessive myocardial apoptosis contributes significantly to cardiac mortality.
- Moderate exercise has demonstrated potential to mitigate cardiac apoptosis.
Purpose of the Study:
- To elucidate the molecular mechanisms by which moderate exercise reduces myocardial apoptosis.
- To identify key signaling pathways and protein expressions involved in exercise-induced cardioprotection.
Main Methods:
- Analysis of protein expression changes in the heart following moderate exercise.
- Investigation of signaling pathways activated by exercise-induced mechanical stress.
- Assessment of mitochondrial-dependent apoptotic factors and their modulation by exercise.
Main Results:
- Moderate exercise increases anti-apoptotic proteins (e.g., IGF-1, Bcl-2) and decreases pro-apoptotic proteins (e.g., PTEN, JNK).
- Exercise activates integrin-mediated signaling pathways (e.g., FAK, Akt/mTORC1, ERK-1/2), leading to an anti-apoptotic response.
- Exercise reduces both extrinsic (e.g., Fas-ligand, caspase-8) and intrinsic (e.g., Bid, caspase-9) apoptotic pathways, decreasing oxidative damage and infarct size.
Conclusions:
- Moderate exercise confers significant cardioprotection by suppressing apoptosis through multiple molecular pathways.
- Exercise modulates key signaling cascades, including PKA-Akt-eNOS, FSTL1-USP10-Notch1, and calcineurin/NFAT, to protect the heart.
- Further research into novel pathways (e.g., Pim-1, Notch) and synergistic therapies is warranted to enhance exercise's anti-apoptotic effects.
Abstract:
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-1α, 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 β and α5 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-α 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 PKCε, PKCδ, and PKCɑ 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 CaMKIIδ, 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.
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