Key result
HIIT upregulates angiogenic and mitochondrial genes, protecting against ischemic cardiac injury.
Why the study?
Physical activity protects the heart against ischemia-reperfusion, and protecting mitochondrial function is a key pathway; the role of exercise preconditioning in this mechanism is important.
Does high-intensity interval training preconditioning reduce cardiac tissue injury and improve mitochondrial biogenesis and angiogenesis following induced myocardial infarction in male rats?
Does high-intensity interval training preconditioning reduce cardiac tissue injury and improve mitochondrial biogenesis and angiogenesis following induced myocardial infarction in male rats?
HIIT preconditioning exerts cardioprotective effects against myocardial infarction in rats by increasing mitochondrial biogenesis and angiogenesis markers.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for HIIT preconditioning in experimental MI; leaves open translation to human prevention strategies.
Background and Objective . Studies have shown that physical activity not only reduces cardiovascular risk factors but also improves cardiac protection against ischemia‐reperfusion. One of the protective pathways of the heart against ischemia is mitochondrial function protection, and the role of exercise preconditioning in this mechanism is important. We investigated the exercise pretraining on mitochondrial biogenesis effect, angiogenesis, and cardiac tissue injury in male rats following stroke. Materials and Methods . Twenty‐four male rats were divided into 4 groups including MI, Sham, HIIT, and HIIT+MI ( N = 6). HIIT and HIIT+MI which underwent high‐intensity interval training (HIIT) for 4 weeks (5 days a week). The training protocol included 10 intervals of 1‐minute running, with 2 minutes rest between each interval. The training intensity was different every week according to the peak treadmill running speed (v peak) percentage of each rat. Isoproterenol injection was used to induce myocardial infarction (MI). Expressions of creatine kinase‐MB (CK‐MB), PGC‐1 α troponin‐I, mitochondrial transcription factor A (TFAM), vascular endothelial growth factor (VEGF), and microRNA 126 (miR‐126) genes were measured. The variables were measured using biochemical and RT‐PCR methods. The significance level ( P value≤0.05) was analyzed using ANOVA test. Results . The results showed that 4 weeks of HIIT training led to a significant increase in PGC‐1 α , TFAm, and VEGF levels in the MI, HIIT, and HIIT+MI groups compared to the sham group ( P = 0.001). HIIT exercises increased miR‐126 in the different groups compared to the sham group; however, it was not significant. Conclusion . The results obtained showed that HIIT exercise exerts cardio‐protective effects to reduce cardiac tissue injury and necrosis against MI. These effects increase mitochondrial biogenesis and angiogenesis by inducing the increased expression of VEGF, TFAM, PGC‐1 α , and miR‐126 genes in the heart tissue. Therefore, HIIT training, as a preconditioning program, was able to protect the cardiac tissue against MI.
No takes yet. Share an insight, caveat, or question.
Heiat et al. (2023) studied Myocardial Infarction (n=24). High-intensity interval training (HIIT) vs. Sham group / MI without HIIT was evaluated on Expression of PGC-1α, TFAM, and VEGF genes in cardiac tissue (p=<0.001). Four weeks of high-intensity interval training significantly increased the expression of VEGF, TFAM, and PGC-1α genes and protected against cardiac tissue injury following induced myocardial infarction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: