Mitochondrial Adaptations in Aging Skeletal Muscle: Implications for Resistance Exercise Training to Treat Sarcopenia

Author:

Jeong Ilyoung1,Cho Eun-Jeong1ORCID,Yook Jang-Soo2,Choi Youngju23ORCID,Park Dong-Ho124ORCID,Kang Ju-Hee125ORCID,Lee Seok-Hun6,Seo Dae-Yun7ORCID,Jung Su-Jeen8,Kwak Hyo-Bum124ORCID

Affiliation:

1. Program in Biomedical Science & Engineering, Department of Biomedical Science, Inha University, Incheon 22212, Republic of Korea

2. Institute of Sports and Arts Convergence, Inha University, Incheon 22212, Republic of Korea

3. Institute of Specialized Teaching and Research, Inha University, Incheon 22212, Republic of Korea

4. Department of Kinesiology, Inha University, Incheon 22212, Republic of Korea

5. Department of Pharmacology, College of Medicine, Inha University, Incheon 22212, Republic of Korea

6. Combat Institute of Australia, Leederville, WA 6007, Australia

7. Basic Research Laboratory, Department of Physiology, College of Medicine, Smart Marine Therapeutic Center, Cardiovascular and Metabolic Disease Core Research Support Center, Inje University, Busan 47392, Republic of Korea

8. Department of Leisure Sports, Seoil University, Seoul 02192, Republic of Korea

Abstract

Sarcopenia, the age-related decline in muscle mass and function, poses a significant health challenge as the global population ages. Mitochondrial dysfunction is a key factor in sarcopenia, as evidenced by the role of mitochondrial reactive oxygen species (mtROS) in mitochondrial biogenesis and dynamics, as well as mitophagy. Resistance exercise training (RET) is a well-established intervention for sarcopenia; however, its effects on the mitochondria in aging skeletal muscles remain unclear. This review aims to elucidate the relationship between mitochondrial dynamics and sarcopenia, with a specific focus on the implications of RET. Although aerobic exercise training (AET) has traditionally been viewed as more effective for mitochondrial enhancement, emerging evidence suggests that RET may also confer beneficial effects. Here, we highlight the potential of RET to modulate mtROS, drive mitochondrial biogenesis, optimize mitochondrial dynamics, and promote mitophagy in aging skeletal muscles. Understanding this interplay offers insights for combating sarcopenia and preserving skeletal muscle health in aging individuals.

Funder

Ministry of Education of the Republic of Korea and the National Research Foundation of Korea

Publisher

MDPI AG

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