Aging-Related Metabolome Analysis of the Masseter Muscle in Senescence-Accelerated Mouse-Prone 8
View abstract on PubMed
Summary
This summary is machine-generated.Aging alters masseter muscle metabolism, impacting frailty and sarcopenia. Key metabolic pathways like glycolysis and polyamine metabolism change, with increased spermidine and Val levels observed in aging mice.
Area Of Science
- Gerontology
- Metabolomics
- Muscle Physiology
Background
- Frailty and sarcopenia are critical in aging, affecting quality of life and transition to long-term care.
- Oral function is increasingly recognized for its link to frailty and sarcopenia.
- Understanding age-related muscle changes is crucial for developing interventions.
Purpose Of The Study
- To investigate age-related changes in metabolites and metabolic pathways within the masseter muscle.
- To identify specific metabolic shifts associated with aging in senescence-accelerated mouse-prone 8 (SAMP8) mice.
Main Methods
- Capillary electrophoresis-mass spectrometry (CE-MS) metabolome analysis was performed on masseter muscle samples from 12-, 40-, and 55-week-old SAMP8 mice.
- Reverse transcription polymerase chain reaction (RT-PCR) was used to confirm enzyme expression in aging-related metabolic pathways.
Main Results
- Significant metabolic fluctuations were observed across the different age groups.
- Key affected metabolic pathways included glycolysis, polyamine metabolism, and purine metabolism.
- Increased levels of spermidine and Valine (Val) were identified as characteristic age-related changes in the masseter muscle.
Conclusions
- Aging in SAMP8 mice significantly alters masseter muscle metabolism, involving glycolysis, polyamine, and purine pathways.
- Elevated spermidine and Val levels in the masseter muscle are distinctive markers of aging compared to lower limb muscles.

