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Fetal muscle extract improves muscle function and performance in aged mice.
Hiu Tung Jessica Lo1,2,3, Tsz Lam Yiu1,2,3, Yujia Wang1,2,3,4
1Musculoskeletal Research Laboratory, Department of Orthopaedics and Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Fetal muscle extract (FSME) shows promise in combating age-related muscle loss. This study found FSME improved muscle mass, strength, and function in aged mice without adverse effects, suggesting a potential novel treatment for sarcopenia.
Area of Science:
- Muscle biology and aging research
- Proteomics and molecular analysis
- Gerontology and regenerative medicine
Background:
- Sarcopenia, the loss of skeletal muscle mass and function, is a significant health issue in aging populations.
- Differential proteomic profiles in fetal muscle development may hold keys to understanding muscle growth.
- Hypothesis: Fetal muscle extract from the hypertrophy stage can mitigate age-related muscle decline.
Purpose of the Study:
- To investigate the potential of fetal sheep muscle extract (FSME) to improve muscle health in aged mice.
- To analyze the proteomic differences between fetal and adult sheep muscle extracts.
- To evaluate the effects of FSME on myoblast proliferation and in vivo muscle function in aged mice.
Main Methods:
- Skeletal muscle extracts from fetal (16-week gestation) and adult sheep were prepared.
- Isobaric tags for relative and absolute quantitation (iTRAQ) and KEGG pathway analysis identified differentially expressed proteins.
- FSME and adult sheep muscle extract (ASME) effects on human myoblast proliferation were assessed.
- Aged mice received intramuscular FSME or vehicle injections for 8 weeks, followed by grip strength and muscle force tests.
- Serum cytokine levels were analyzed using multiplex assays.
Main Results:
- iTRAQ analysis revealed significant differences in protein expression between FSME and ASME, with many proteins related to muscle development.
- FSME significantly promoted myoblast proliferation (+300%) without cytotoxicity.
- In aged mice, FSME treatment increased lean mass (+10%), grip strength (+50%), and fatigue resistance.
- Histological analysis showed no significant difference in muscle cross-sectional area between FSME and control groups.
- FSME treatment led to a significant reduction in specific circulating inflammatory cytokines, including IL-12, G-CSF, KC, and RANTES.
Conclusions:
- This study provides the first evidence of beneficial effects of fetal muscle extract on muscle health in aged mice.
- FSME demonstrates potential as a therapeutic agent for age-related muscle decline and sarcopenia.
- Further research into the active components of FSME could lead to novel sarcopenia treatments.
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