Advanced glycation end-products accumulate preferentially in type I muscle fibers of aging adults but are unchanged by training and polyphenol supplementation.
Abstract
Advanced glycation end-products (AGEs) accumulate with age and may contribute to skeletal muscle decline, yet their distribution within muscle compartments is unknown. Resistance training (RT) and high-intensity interval training (HIIT) improve muscle function, but their effects on muscle AGEs remain unexplored. Polyphenols have antioxidant properties, which could limit AGE formation. This study investigated AGE accumulation in different muscle compartments and whether a 12-week RT + HIIT intervention, with or without polyphenol supplementation could modify AGE levels. Forty-one healthy middle-aged and older adults (55-70 years) were randomized to receive a polyphenol-rich berry extract or placebo for 30 days, followed by 12 weeks of supervised RT + HIIT. Vastus lateralis biopsies were collected before and after the intervention and analyzed for subtypes of AGEs using immunofluorescence. AGE immunoreactivity was quantified in type I and type II fibers and in the extracellular matrix (ECM). AGE immunoreactivity was higher in type I than type II fibers (p < 0.0001) and most pronounced in the ECM (p < 0.05 vs. both fiber types). AGE signals did not differ between sexes and were unrelated to age or plasma IL-6. Neither training nor polyphenol supplementation altered AGE content in fibers or ECM. These findings provide the first evidence of fiber-type-associated localization of AGE immunoreactivity in humans. The absence of change following 12 weeks of RT and HIIT, with or without polyphenol, suggests that AGE turnover in skeletal muscle is limited in short-term interventions, highlighting the need for longer strategies to reduce AGE accumulation.
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Research summary
The study claims that advanced glycation end-products (AGEs) accumulate preferentially in type I muscle fibers of aging adults and are unaffected by resistance training and polyphenol supplementation. This research is relevant as it explores the accumulation of AGEs, which may contribute to age-related muscle decline, and investigates potential interventions that could influence this process, addressing a root cause of aging-related muscle deterioration.
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