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The 5,7-Dimethoxyflavone Suppresses Sarcopenia by Regulating Protein Turnover and Mitochondria Biogenesis-Related
Changhee Kim1, Jae-Kwan Hwang1
1Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Korea.
Abstract:
Sarcopenia is a muscle disease featured by the loss of muscle mass and dysfunction with advancing age. The 5,7-dimethoxyflavone (DMF), a major flavone found in Kaempferia parviflora, has biological activities, including anti-diabetes, anti-obesity, and anti-inflammation. However, its anti-sarcopenic effect remains to be elucidated. This current study investigated the inhibitory activity of DMF on sarcopenia. Eighteen-month-old mice were orally administered DMF at the dose of 25 mg·kg-1·day-1 or 50 mg·kg-1·day-1 for 8 weeks. DMF not only stimulated grip strength and exercise endurance but also increased muscle mass and volume. Besides, DMF stimulated the phosphatidylinositol 3-kinase-Akt pathway, consequently activating the mammalian target of rapamycin-eukaryotic initiation factor 4E-binding protein 1-70-kDa ribosomal protein S6 kinase pathway for protein synthesis. DMF reduced the mRNA expression of E3 ubiquitin ligase- and autophagy-lysosomal-related genes involved in proteolysis via the phosphorylation of Forkhead box O3. DMF upregulated peroxisome proliferator-activated receptor-gamma coactivator 1 alpha, nuclear respiratory factor 1, and mitochondrial transcription factor A along with the increase of relative mitochondrial DNA content. DMF alleviated inflammatory responses by reducing the tumor necrosis factor-alpha and interleukin-6 serum and mRNA levels. Collectively, DMF can be used as a natural agent to inhibit sarcopenia via improving protein turnover and mitochondria function.
Insights
5,7-dimethoxyflavone (DMF) effectively combats sarcopenia, the age-related loss of muscle mass and function. This natural compound enhances muscle strength, mass, and mitochondrial function while reducing inflammation and protein breakdown.
Area of Science:
- Gerontology
- Muscle Biology
- Pharmacology
Background:
- Sarcopenia is characterized by age-related muscle mass loss and dysfunction.
- 5,7-dimethoxyflavone (DMF), derived from Kaempferia parviflora, exhibits anti-diabetic, anti-obesity, and anti-inflammatory properties.
- The anti-sarcopenic effects of DMF are not yet fully understood.
Purpose of the Study:
- To investigate the potential of DMF as an inhibitor of sarcopenia.
- To elucidate the molecular mechanisms underlying DMF's effects on muscle health.
Main Methods:
- Eighteen-month-old mice were administered DMF (25 or 50 mg·kg⁻¹·day⁻¹) orally for 8 weeks.
- Evaluated grip strength, exercise endurance, muscle mass, and volume.
- Analyzed molecular pathways including Akt/mTOR, proteolysis markers (E3 ubiquitin ligase, autophagy), mitochondrial biogenesis factors, and inflammatory cytokines (TNF-α, IL-6).
Main Results:
- DMF administration significantly improved grip strength and exercise endurance.
- Increased muscle mass and volume were observed in DMF-treated mice.
- DMF activated the Akt/mTOR pathway, enhanced protein synthesis, reduced proteolysis via FOXO3 phosphorylation, upregulated mitochondrial biogenesis factors, and decreased serum and mRNA levels of TNF-α and IL-6.
Conclusions:
- DMF demonstrates significant anti-sarcopenic activity.
- DMF improves muscle function and mass by modulating protein turnover and enhancing mitochondrial biogenesis.
- DMF alleviates inflammation, suggesting its potential as a natural therapeutic agent for sarcopenia.
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