Effect of taurine associated gold nanoparticles on oxidative stress in muscle of mice exposed to overuse model.
Anand ThirupathiHelen R SoratoPaulo Roberto L da SilvaAdriani Paganini DamianiVanessa Moraes de AndradePaulo Cesar Lock SilveiraRenata Tiscoski NesiMarcos Marques da Silva PaulaRicardo Aurino PinhoPublished in: Anais da Academia Brasileira de Ciencias (2021)
Muscle overuse and its consequent muscle damage has no cure. Therefore, the present study aimed to investigate the regulatory role of tau-AuNPs on muscle recovery of muscle overuse model. The animals (Male Swiss mice) were randomly divided into four groups: Control (Ctr; n=6); tau-AuNPs (n=6); overuse (n=6); and overuse plus tau-AuNPs (n=6). Exercise sessions were performed for 21 consecutive days, and one exercise model was applied daily in the following sequence: low intensity, moderate intensity, and high intensity. The mice were then sacrificed. The quadriceps muscles were surgically removed for subsequent biochemical analysis (oxidative stress parameters, DNA damage markers and muscle differentiation protein). The overuse group significantly increased the oxidative stress parameters and DNA damage markers, whereas tau-AuNPs significantly decreased the oxidative stress parameters in the overuse animal model. However, there were no significant differences observed between overuse group and overuse plus tau-AuNPs administrated group in relation to DNA damage markers including DNA damage frequency and index levels when compared to control and tau-AuNPs groups. Muscle differentiation protein Myf-5 was increased in the overuse plus tau-AuNPs administration group when compared to control group. In conclusion, tau-AuNPs had significant effect on reducing oxidative stress parameters and increasing myogenic regulatory protein Myf-5 in the overuse group. However, it did not have significant effect on reducing DNA damage.
Keyphrases
- dna damage
- oxidative stress
- high intensity
- skeletal muscle
- dna repair
- cerebrospinal fluid
- gold nanoparticles
- diabetic rats
- induced apoptosis
- resistance training
- ischemia reperfusion injury
- physical activity
- type diabetes
- transcription factor
- amino acid
- protein protein
- metabolic syndrome
- small molecule
- signaling pathway