Aerobic Exercise Training Elevates Circulating sRAGE via Modulation of Sheddase Regulation in Adults with Type 2 Diabetes
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Objective
Soluble receptors for advanced glycation end-products (sRAGE) and Toll-like receptor 4 (sTLR4) function as decoy receptors that blunt proinflammatory signaling in metabolic disease. This study examined the effects of 12 weeks of aerobic exercise (AE) training on circulating sRAGE, sTLR4, and associated skeletal muscle sheddase regulators in adults with type 2 diabetes mellitus (T2DM).
Methods
Thirty-three sedentary adults with T2DM (age 40–75 yrs) were randomized to AE (n=20) or control (CON; n=13). AE participants completed supervised aerobic training (60 min/day, 5 days/week) at 70% VO₂peak. Pre- and post-intervention assessments included oral glucose tolerance testing (OGTT), DXA, VO₂peak, and a standardized acute aerobic exercise trial with blood and skeletal muscle sampling. Circulating sRAGE, sTLR4, hsCRP, and skeletal muscle expression of TLR2/4, RAGE, MMP2/9, ADAM10, and TIMP1/3 were quantified.
Results
AE increased circulating sRAGE by +25.7% (P=0.005), with 83% of participants demonstrating a positive response. hsCRP decreased (−6.5%, P=0.04), while sTLR4 remained unchanged. AE also improved VO₂peak (+6.9%, P=0.001) and reduced body fat (−3.8%, P=0.00002). In skeletal muscle, TLR4 protein approached significance (−27.4%, P=0.10), and the TIMP3:ADAM10 ratio declined markedly (−87%, P<0.000001), suggesting reduced sheddase inhibition. No significant changes were observed in ADAM10 activity or MMP/TLR protein levels. sRAGE changes correlated with MMP9 expression (r=0.747, P=0.013).
Conclusions
AE training increases circulating sRAGE and improves systemic inflammatory profiles in adults with T2DM, potentially via modulation of sheddase regulatory balance. These findings identify AE training as a non-pharmacological strategy to enhance endogenous anti-inflammatory defenses in T2DM through sRAGE regulation.
