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. 2019 May 9:10:554.
doi: 10.3389/fphys.2019.00554. eCollection 2019.

Muscle and Systemic Molecular Responses to a Single Flywheel Based Iso-Inertial Training Session in Resistance-Trained Men

Affiliations

Muscle and Systemic Molecular Responses to a Single Flywheel Based Iso-Inertial Training Session in Resistance-Trained Men

Giosuè Annibalini et al. Front Physiol. .

Abstract

Growing evidence points to the effectiveness of flywheel (FW) based iso-inertial resistance training in improving physical performance capacities. However, molecular adaptations induced by FW exercises are largely unknown. Eight resistance-trained men performed 5 sets of 10 maximal squats on a FW device. Muscle biopsies (fine needle aspiration technique) and blood samples were collected before (t0), and 2 h (t1) after FW exercise. Blood samples were additionally drawn after 24 h (t2) and 48 h (t3). Paired samples t-tests revealed significant increases, at t1, of mRNA expression of the genes involved in inflammation, in both muscle (MCP-1, TNF-α, IL-6) and peripheral blood mononuclear cells (IkB-α, MCP-1). Circulating extracellular vesicles (EVs) and EV-encapsulated miRNA levels (miR-206, miR-146a) significantly increased at t1 as well. Conversely, muscle mRNA level of genes associated with muscle growth/remodeling (IGF-1Ea, cyclin D1, myogenin) decreased at t1. One-way repeated measure ANOVAs, with Bonferroni corrected post-hoc pairwise comparisons, revealed significant increases in plasma concentrations of IL-6 (t1; t2; t3) and muscle creatine kinase (t1; t2), while IGF-1 significantly increased at t2 only. Our findings show that, even in experienced resistance trained individuals, a single FW training session modifies local and systemic markers involved in late structural remodeling and functional adaptation of skeletal muscle.

Keywords: circulating miRNAs; extracellular vesicles; growth factors; inflammation; iso-inertial exercise.

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Figures

Figure 1
Figure 1
Experimental design of the flywheel training session (4th visit) and of the following blood draws (5th and 6th visit). The time schedule of pre- (t0) and post-exercise (t1; t2; t3) samplings is shown below the timeline. FNA, fine needle aspiration.
Figure 2
Figure 2
Fold change in IkBα, MCP-1, TNF-α, IL-6, IL-6R (A), IGF-1 isoforms (B) and cyclin D1, myogenin and MRF4 (C) mRNA levels in muscle FNA samples obtained 2 h post-exercise (t1) compared to the pre-exercise (t0) (represented by the dotted line). Values are mean ± SE. *, significant difference from t0 (p < 0.05); **, highly significant difference from t0 (p < 0.01); n = 8.
Figure 3
Figure 3
Quantification of IL-6 (A), CKM (B), and IGF-1 (C) plasma levels before (t0) and after (t1: 2 h; t2: 24 h; t3: 48 h) the flywheel training session. Values are mean ± SE. *, significant difference from t0 (p < 0.05); **, highly significant difference from t0 (p < 0.01); n = 8.
Figure 4
Figure 4
Fold change in IkB-α, MCP-1, TNF-α, IL-6, IL-6R mRNA levels in PBMC isolated 2 h post-exercise (t1) compared to pre-exercise (t0) (represented by the dotted line). Values are mean ± SE. *, significant difference from t0 (p < 0.05); n = 8.
Figure 5
Figure 5
Post-exercise (t1) vs. pre-exercise (t0) nanoparticle tracking assay of circulating EVs (A) and fold change in miRNA levels in circulating EVs (B). Pre-exercise values within (B) are represented by the dotted line. Values are mean ± SE. **, highly significant difference from t0 (p < 0.01); n = 8.

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