Effects of exercises with different durations and intensities on mitochondrial autophagy and FUNDC1 expression in rat skeletal muscles.
- Author:
Liang YU
1
;
Xiao-Yu SHI
1
;
Zi-Ming LIU
2
;
Zhen WANG
1
;
Lin LI
1
;
Jiu-Xiang GAO
1
;
Xiao-Ran LIU
3
;
Rui-Yuan WANG
4
Author Information
1. College of Human Movement Sciences, Beijing Sports University, Beijing 100084, China.
2. Tennis Sports Management Center, General Administration of Sport, Beijing 100010, China.
3. School of Kinesiology and Health, Capital University of Physical Education and Sports, Beijing 100191, China.
4. College of Human Movement Sciences, Beijing Sports University, Beijing 100084, China. wangruiyuan2018@sina.com.
- Publication Type:Journal Article
- MeSH:
Animals;
Autophagy;
Exercise Therapy;
Humans;
Male;
Membrane Proteins/physiology*;
Mitochondria;
Mitochondrial Proteins/physiology*;
Muscle, Skeletal/metabolism*;
Rats;
Rats, Sprague-Dawley
- From:
Acta Physiologica Sinica
2020;72(5):631-642
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the present study was to investigate the effects of exercises with different durations and intensities on mitochondrial autophagy and FUNDC1 in rat skeletal muscles. Sixty male Sprague-Dawley rats were randomly divided into 2- and 4-week control groups (Con), moderate-intensity exercise groups (M-ex groups, treadmill exercise, 16 m/min, 1 h/d, 6 d/week), and high-intensity exercise groups (Hi-ex groups, treadmill exercise, 35 m/min, 20 min/d, 6 d/week). The bilateral soleus muscles were separated after the intervention, and paraffin sections were prepared for transmission electron microscopy. ELISA method was used to detect the content of citrate synthase (CS). The co-localizations of microtubule-associated protein 1 light chain 3 (LC3)/cytochrome c oxidase IV (COX-IV), FUNDC1/COX-IV and LC3/FUNDC1 were observed by immunofluorescent staining in frozen sections. The skeletal muscle mitochondria were extracted, and the expression of autophagy-related proteins, including AMPKα, p-AMPKα, Unc-51 like kinase 1 (ULK1), FUNDC1, LC3 and p62, were detected by Western blot. The results showed that exercise increased mitochondrial function, i.e. peroxisome proliferator-activated receptor γ co-activator-1α (PGC-1α), COX-I protein expression levels and CS content. There was no difference of mitochondrial function parameters between 2-week M-ex and 2-week Hi-ex groups, while mitochondrial function of 4-weeks Hi-ex group was significantly lower than that of 4-week M-ex group. Under the same exercise intensity, mitochondrial autophagy activation in skeletal muscle of 4-week exercise was higher than that in 2-week exercise group; Under the same duration of exercise, mitochondrial autophagy activation of Hi-ex group was higher than that in M-ex group. Both 2- and 4-week exercise intervention increased LC3/COX-IV, COX-IV/FUNDC1, and FUNDC1/LC3 co-localizations. Exercise increased LC3-II/LC3-I ratio, down-regulated p62 protein expression level, up-regulated FUNDC1, ULK1 protein expression levels and AMPKα phosphorylation, and the changes of these proteins in 4-week Hi-ex group were significantly greater than those in 4-week M-ex group. These results suggest exercise induces mitochondrial autophagy in skeletal muscles, and the activity of autophagy is related to the duration and intensity of exercise. The induction mechanism of exercise may involve the mediation of FUNDC1 expression through AMPK-ULK1 pathway.
