Circulating extracellular vesicle characteristics differ between men and women following 12 weeks of concurrent exercise training.
Christopher K KarglAdam J SterczalaDaniella SantucciWilliam R ConkrightKellen T KrajewskiBrian J MartinJulie P GreevesThomas J O'LearySophie L WardleAmrita SahuFabrisia AmbrosioBradley C NindlPublished in: Physiological reports (2024)
Concurrent resistance and endurance exercise training (CET) has well-studied benefits; however, inherent hormonal and genetic differences alter adaptive responses to exercise between sexes. Extracellular vesicles (EVs) are factors that contribute to adaptive signaling. Our purpose was to test if EV characteristics differ between men and women following CET. 18 young healthy participants underwent 12-weeks of CET. Prior to and following CET, subjects performed an acute bout of heavy resistance exercise (AHRET) consisting of 6 × 10 back squats at 75% 1RM. At rest and following AHRET, EVs were isolated from plasma and characteristics and miRNA contents were analyzed. AHRET elevated EV abundance in trained men only (+51%) and AHRET-induced changes were observed for muscle-derived EVs and microvesicles. There were considerable sex-specific effects of CET on EV miRNAs, highlighted by larger variation following the 12-week program in men compared to women at rest. Pathway analysis based on differentially expressed EV miRNAs predicted that AHRET and 12 weeks of CET in men positively regulates hypertrophy and growth pathways more so than in women. This report highlights sex-based differences in the EV response to resistance and concurrent exercise training and suggests that EVs may be important adaptive signaling factors altered by exercise training.
Keyphrases
- skeletal muscle
- polycystic ovary syndrome
- middle aged
- high intensity
- resistance training
- locally advanced
- gestational age
- liver failure
- drug induced
- pregnancy outcomes
- physical activity
- squamous cell carcinoma
- radiation therapy
- randomized controlled trial
- gene expression
- body composition
- clinical trial
- high glucose
- dna methylation
- study protocol
- intensive care unit
- endothelial cells
- copy number