AI Article Synopsis

  • The study investigates how high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) impact the expression of Rac1 and PAK1 proteins, which play roles in glucose uptake in skeletal muscle.
  • The methods involved measuring mRNA and protein expressions using qPCR and reverse-phase protein microarray in fast-type (GC) and slow-type (SOL) muscles of rats after exercise.
  • Results showed that HIIT significantly increased Rac1 and PAK1 mRNA expression in fast-type muscle compared to MICT and control groups, suggesting HIIT may offer new therapeutic options for metabolic disease treatment.

Article Abstract

Purpose: Rac1 and its downstream target PAK1 are novel regulators of insulin and exercise-induced glucose uptake in skeletal muscle. However, it is not yet understood how different training intensities affect the expression of these proteins. Therefore, we studied the effects of (HIIT) and (MICT) on Rac1 and PAK1 expression in fast-type (, GC) and slow-type (, SOL) muscles in rats after HIIT and MICT swimming exercises.

Methods: The mRNA expression was determined using qPCR and protein expression levels with reverse-phase protein microarray (RPPA).

Results: HIIT significantly mRNA expression in GC compared to MICT ( = 0.003) and to the control group (CON) ( = 0.001). At the protein level Rac1 was in GC in both training groups, but only the difference between HIIT and CON was significant ( = 0.02). HIIT caused significant of mRNA expression in GC compared to MICT ( = 0.007) and to CON ( = 0.001). At the protein level, HIIT increased PAK1 expression in GC compared to MICT and CON (by ∼17%), but the difference was not statistically significant ( = 0.3, = 0.2, respectively). There were no significant differences in the Rac1 or PAK1 expression in SOL between the groups.

Conclusion: Our results indicate that HIIT, but not MICT, Rac1 and PAK1 mRNA expression and the protein expression of especially Rac1 but only in fast-type muscle. These exercise training findings may reveal new therapeutic targets to treat patients with metabolic diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711069PMC
http://dx.doi.org/10.3389/fphys.2020.584661DOI Listing

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