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DOI 10.1080/02701367.2022.2060926

Медицинская библиотека · Research quarterly for exercise and sport · 2022

Plasma α-Actin as an Early Marker of Muscle Damage After Repeated Bouts of Eccentric Cycling.

Jannas-Vela Sebastian, Bustamante Alvaro, Zbinden-Foncea Hermann, Peñailillo Luis

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Аннотация

Purpose: This study aimed to examine the changes in skeletal muscle (SM) α-actin, myoglobin (Mb) and hydroxyproline (HP) in plasma and other indirect markers of muscle damage after repeated bouts of eccentric cycling.

Methods

Ten healthy men (23.3 ± 2.8 years) performed two 30-min eccentric cycling bouts at 100% of maximal concentric power output (230.7 ± 36.9 W) separated by 2 weeks (ECC1 and ECC2). Maximal voluntary isometric contraction (MVIC) peak force of the knee extensor muscles, muscle soreness (SOR), pain pressure threshold (PPT) and plasma levels of SM α-actin, Mb, and HP were measured before, 0.5, 3, 24-168 h after each cycling bout.

Results

MVIC peak force decreased on average 10.7 ± 13.1% more after ECC1 than ECC2. SOR was 80% greater and PPT was 12-14% lower after ECC1 than ECC2. Plasma SM α-actin levels increased at 0.5, 3, and 24-72 h after ECC1 (26.1-47.9%), and SM α-actin levels at 24 h after ECC1 were associated with muscle strength loss (r = -0.56, P = .04) and SOR (r = 0.88, P = .001). Mb levels increased at 0.5, 3, and 24 h after ECC1 (200-502%). However, Mb levels at 24 h after ECC1were not associated with muscle strength loss and SOR. HP levels remained unchanged after ECC1. ECC2 did not increase SM α-actin, Mb and HP levels.

Conclusion

Our results indicate that α-actin could be used as a potential marker for the early identification of SM damage due to its early appearance in plasma and its association with other indirect markers of muscle damage.

Для цитирования: Jannas-Vela Sebastian, Bustamante Alvaro, Zbinden-Foncea Hermann, Peñailillo Luis. Plasma α-Actin as an Early Marker of Muscle Damage After Repeated Bouts of Eccentric Cycling.. Research quarterly for exercise and sport. 2022. DOI: 10.1080/02701367.2022.2060926.

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