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Effect of High-Intensity Interval Training on Cardiac Apoptosis Markers in Methamphetamine-Dependent Rats.
Hadi Shahrabadi1, Amir Hossein Haghighi1, Roya Askari1
1Department of Exercise Physiology, Faculty of Sport Sciences, Hakim Sabzevari University, Sabzevar 9617976487, Iran.
Chronic methamphetamine use harms heart tissue by increasing apoptosis. High-intensity interval training (HIIT) may protect cardiac function by reducing these harmful effects in methamphetamine-dependent rats.
Area of Science:
- Sports science
- Cardiology
- Molecular biology
Background:
- Chronic methamphetamine (METH) use is linked to cardiac apoptosis, heart failure, and sudden cardiac death.
- High-intensity interval training (HIIT) has shown potential in reducing cardiac apoptosis, but its molecular mechanisms in METH-dependent individuals are not well understood.
Purpose of the Study:
- To investigate the effects of HIIT on cardiac apoptosis markers in a rat model of chronic methamphetamine dependence.
- To explore the molecular mechanisms underlying cardiac apoptosis and potential protective effects of HIIT.
Main Methods:
- Rats were administered METH for 21 days.
- The METH-HIIT group underwent 8 weeks of HIIT (5 sessions/week).
- Gene expression of apoptosis markers (caspase-3) and related proteins (melusin, FAK, IQGAP1) in left ventricular tissue was analyzed.
Main Results:
- METH exposure significantly increased caspase-3 expression and decreased melusin, FAK, and IQGAP1 in cardiac tissue.
- HIIT intervention in METH-dependent rats led to decreased caspase-3 and increased melusin and FAK gene expression compared to METH-only groups.
- IQGAP1 expression was higher in the METH-HIIT group than the METH group, but similar to the METH-control group.
Conclusions:
- Twenty-one days of METH exposure elevates cardiac apoptosis markers in rats.
- HIIT demonstrates a potential protective effect against METH-induced cardiac apoptosis, as evidenced by the modulation of key molecular markers.
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