Abstract

ABSTRACT Objective: To study the effects of exhaustive exercise and contusion on autophagy-related factors Beclin1, LC3 and PINK1 expression in the skeletal muscle of rats. Methods: Forty-two male SD rats were randomly divided into 7 groups, 6 rats in each group: C, D0, D24, D48, E0, E24, and E48. Each group of rats was killed and dissected at the different respective time points specified above. The whole quadriceps femoris of the left hind limbs were removed and divided into two parts, one for mRNAs of Beclin1, LC3 and PINK1 by real-time fluorescent quantitative PCR, and the other for LC3 protein by Western blotting. Results: Compared with group C, the contents of Beclin1 mRNA, PINK1 mRNA, and LC3 mRNA in the immediate exhaustive exercise group (E0) were significantly reduced p<0.01. However, the levels of PINK1 mRNA, LC3 mRNA, and LC3 protein in skeletal muscle cells increased significantly in the 48 hours after exhaustion (E48) p<0.05, suggesting that cell autophagy had an increasing trend during the recovery period. Meanwhile, compared with the C group, the contents of Beclin1 mRNA, PINK1 mRNA, and LC3 mRNA in the immediate blunt contusion group (D0) increased significantly p<0.01 and were followed by a downward trend. Conclusion: Generally, there were differences between the blunt contusion and exhausted exercise models at each recovery phase. The gene expression of the autophagy-related factors was not high in the early exhaustive exercise recovery phase and subsequently followed an upward trend. But the above factors increased significantly in the immediate and early recovery phases after blunt contusion. Injury from blunt contusion may be more severe than exhaustive exercise-induced-injury, so the autophagy starts earlier according to the changes in autophagy-related factors. Level of evidence III; Therapeutic studies investigating the results of treatment.

Highlights

  • After skeletal muscle injury, the body will repair the damaged part

  • The results of qRT-PCR showed that compared with group C, the contents of Beclin[1] mRNA, PINK1 mRNA, and LC3 mRNA in the immediate exhausted exercise group (E0) significantly reduced (p

  • In our rat models with different phases, we found that the contents of Beclin[1] mRNA, PINK1 mRNA, and LC3 mRNA in the immediate exhausted exercise group (E0) significantly reduced by compared with group C, indicating that the level of cellular autophagy were not high at the early recovery phase of exhausted exercise

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Summary

Introduction

The body will repair the damaged part. In addition to muscle satellite cells’ repair, autophagy is an important repair procedure of skeletal muscle injury.[1,2] Autophagy can remove damaged cells and is an active protective measure for cells.[3] Autophagy of skeletal muscle cells can transport damaged, degraded or aging proteins and organelle into the lysosome for digestion and degradation, which can provide certain energy and synthetic substrates for muscle fiber regeneration, and inhibit skeletal muscle cell apoptosis.[4] The resynthesis of mitochondria and contractile proteins during the adaptation of skeletal muscle has a certain effect on injured muscle cells. Mitochondrial autophagy of skeletal muscle has received wide attention in the repair process of skeletal muscle injury.[5]

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