An Amino Acid Mixture to Counteract Skeletal Muscle Atrophy: Impact on Mitochondrial Bioenergetics

被引:0
|
作者
Bellanti, Francesco [1 ]
Lo Buglio, Aurelio [1 ]
Pannone, Giuseppe [2 ]
Pedicillo, Maria Carmela [2 ]
De Stefano, Ilenia Sara [2 ]
Pignataro, Angela [2 ]
Capurso, Cristiano [1 ]
Vendemiale, Gianluigi [1 ]
机构
[1] Univ Foggia, Dept Med & Surg Sci, I-71122 Foggia, Italy
[2] Univ Foggia, Dept Clin & Expt Med, I-71122 Foggia, Italy
关键词
immobilization; cardiotoxin; sarcopenia; amino acids; PROTEIN-SYNTHESIS; SUPPLEMENTATION; EXERCISE; DISUSE; RECOVERY; DAMAGE;
D O I
10.3390/ijms25116056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skeletal muscle atrophy (SMA) is caused by a rise in muscle breakdown and a decline in protein synthesis, with a consequent loss of mass and function. This study characterized the effect of an amino acid mixture (AA) in models of SMA, focusing on mitochondria. C57/Bl6 mice underwent immobilization of one hindlimb (I) or cardiotoxin-induced muscle injury (C) and were compared with controls (CTRL). Mice were then administered AA in drinking water for 10 days and compared to a placebo group. With respect to CTRL, I and C reduced running time and distance, along with grip strength; however, the reduction was prevented by AA. Tibialis anterior (TA) muscles were used for histology and mitochondria isolation. I and C resulted in TA atrophy, characterized by a reduction in both wet weight and TA/body weight ratio and smaller myofibers than those of CTRL. Interestingly, these alterations were lightly observed in mice treated with AA. The mitochondrial yield from the TA of I and C mice was lower than that of CTRL but not in AA-treated mice. AA also preserved mitochondrial bioenergetics in TA muscle from I and C mice. To conclude, this study demonstrates that AA prevents loss of muscle mass and function in SMA by protecting mitochondria.
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页数:16
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