Restorative effects of (+)-epicatechin in a rodent model of aging induced muscle atrophy: underlying mechanisms

被引:0
|
作者
Ramirez-Sanchez, Israel [1 ,2 ]
Navarrete-Yanez, Viridiana [2 ]
Ramirez, Lucia [1 ]
Galera, Leonor [2 ]
Mendez-Bolaina, Enrique [3 ]
Najera, Veronica [1 ]
Ceballos, Guillermo [2 ]
Villarreal, Francisco [1 ,4 ]
机构
[1] UCSD, Sch Med, La Jolla, CA 92093 USA
[2] Escuela Super Med, IPN, Secc Estudios Posgrad & Invest, Plan de San Luis & Salvador Diaz Miron S-N, Mexico City 11340, Mexico
[3] Univ Veracruzana, Fac Ciencias Quim, Orizaba, Mexico
[4] VA San Diego Hlth Care Syst, San Diego, CA USA
关键词
SKELETAL-MUSCLE; SARCOPENIA; MYOSTATIN; (-)-EPICATECHIN; APOPTOSIS; COCOA;
D O I
10.1039/d3fo04004f
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
Sarcopenia is a progressive and generalized age-related skeletal muscle (SkM) disorder characterized by the accelerated loss of muscle mass (atrophy) and function. SkM atrophy is associated with increased incidence of falls, functional decline, frailty and mortality. In its early stage, SkM atrophy is associated with increased pro-inflammatory cytokine levels and proteasome-mediated protein degradation. These processes also link to the activation of atrophy associated factors and signaling pathways for which, there is a lack of approved pharmacotherapies. The objective of this study, was to characterize the capacity of the flavanol (+)-epicatechin (+Epi) to favorably modulate SkM mass and function in a rat model of aging induced sarcopenia and profile candidate mechanisms. Using 23 month old male Sprague-Dawley rats, an 8 weeks oral administration of the +Epi (1 mg per kg per day in water by gavage) was implemented while control rats only received water. SkM strength (grip), treadmill endurance, muscle mass, myofiber area, creatine kinase, lactate dehydrogenase, troponin, alpha-actin, tumor necrosis factor (TNF)-alpha and atrophy related endpoints (follistatin, myostatin, NF kappa B, MuRF 1, atrogin 1) were quantified in plasma and/or gastrocnemius. We also evaluated effects on insulin growth factor (IGF)-1 levels and downstream signaling (AKT/mTORC1). Treatment of aged rats with +Epi, led to significant increases in front paw grip strength, treadmill time and SkM mass vs. controls as well as beneficial changes in makers of myofiber integrity. Treatment significantly reversed adverse changes in plasma and/or SkM TNF-alpha, IGF-1, atrophy and protein synthesis related endpoints vs. controls. In conclusion, +Epi has the capacity to reverse sarcopenia associated detrimental changes in regulatory pathways leading to improved SkM mass and function. Given these results and its recognized safety and tolerance profile, +Epi warrants consideration for clinical trials. Sarcopenia is a progressive and generalized age-related skeletal muscle (SkM) disorder characterized by the accelerated loss of muscle mass (atrophy) and function.
引用
收藏
页码:3669 / 3679
页数:11
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