High‐Intensity Interval Training Mitigates Sarcopenia and Suppresses the Myoblast Senescence Regulator EEF1E1

• Published in: Journal of cachexia, sarcopenia and muscle sarcopenia and muscle, 2024-12, Vol.15 (6), p.2574-2585
• Main Authors: Dun, Yaoshan, Zhang, Wenliang, Du, Yang, Xie, Kangling, Liu, Yuan, Li, Cui, Qiu, Ling, Fu, Siqian, Olson, Thomas P., Long, Yuqiong, You, Baiyang, Liu, Suixin
• Format: Article
• Language: English
• Subjects: Adult; Aged; Animals; Autophagy; Biomarkers; Cellular Senescence; EEF1E1; Female; Fitness equipment; High-Intensity Interval Training - methods; high‐intensity interval training; Humans; Interval training; Intervention; Laboratory animals; Male; Mice; Musculoskeletal system; Myoblasts - metabolism; Normal distribution; Older people; Original; Peptide Elongation Factor 1 - metabolism; Plasma; Proteins; Proteomics - methods; Running; Sarcopenia; Sarcopenia - metabolism; Sarcopenia - prevention & control; Sarcopenia - therapy; Senescence; Workloads
• ISSN: 2190-5991; 2190-6009; 2190-6009
• DOI: 10.1002/jcsm.13600

ABSTRACT Background The optimal exercise regimen for alleviating sarcopenia remains uncertain. This study aimed to investigate the efficacy of high‐intensity interval training (HIIT) over moderate‐intensity continuous training (MICT) in ameliorating sarcopenia. Methods We conducted a randomized crossover trial to evaluate plasma proteomic reactions to acute HIIT (four 4‐min high‐intensity intervals at 70% maximal capacity alternating with 4 min at 30%) versus MICT (constant 50% maximal capacity) in inactive adults. We explored the relationship between a HIIT‐specific protein relative to MICT, identified via comparative proteomic analysis, eukaryotic translation elongation factor 1 epsilon 1 (EEF1E1) and sarcopenia in a paired case–control study of elderly individuals (aged over 65). Young (3 months old) and aged (20 months old) mice were randomized to sedentary, HIIT and MICT groups (five sessions/week for 4 weeks; n = 8 for each group). Measurements included skeletal muscle index, hand grip strength, expression of atrophic markers Atrogin1 and MuRF1 and differentiation markers MyoD, myogenin and MyHC‐II via western blotting. We examined the impact of EEF1E1 siRNA and recombinant protein on D‐galactose‐induced myoblast senescence, measuring senescence‐associated β‐galactosidase and markers like p21 and p53. Results The crossover trial, including 10 sedentary adults (32 years old, IQR 31–32) demonstrated significant alterations in the abundance of 21 plasma proteins after HIIT compared with MICT. In the paired case–control study of 84 older adults (84 years old, IQR 69–81; 52% female), EEF1E1 was significantly increased in those with sarcopenia compared to those without (14.68 [95%CI, 2.02–27.34] pg/mL, p = 0.03) and was associated with skeletal muscle index (R2 = 0.51, p