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1.
Exp Gerontol ; 45(11): 882-95, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20705127

RESUMEN

Aging is associated with increased oxidative stress. Muscle levels of oxidative stress are further elevated with exercise. The purpose of this study was to determine if dietary antioxidant supplementation would improve muscle function and cellular markers of oxidative stress in response to chronic repetitive loading in aging. The dorsiflexors of the left limb of aged and young adult Fischer 344 Brown×Norway rats were loaded 3 times weekly for 4.5 weeks using 80 maximal stretch-shortening contractions per session. The contra-lateral limb served as the intra-animal control. The rats were randomly assigned to a diet supplemented with Vitamin E and Vitamin C or normal non-supplemented rat chow. Biomarkers of oxidative stress were measured in the tibialis anterior muscle. Repetitive loading exercise increased maximal isometric force, negative work and positive work in the dorsiflexors of young adult rats. Only positive work increased in the aged animals that were supplemented with Vitamin E and C. Markers of oxidative stress (H(2)O(2), total GSH, GSH/GSSG ratio, malondialdehyde and 8-OHdG) increased in the tibialis anterior muscles from aged and young adult animals with repetitive loading, but Vitamin E and C supplements attenuated this increase. MnSOD activity increased with supplementation in the young adult animals. CuZnSOD and catalase activity increased with supplementation in young adult and aged animals and GPx activity increased with exercise in the non-supplemented young adult and aged animals. The increased levels of endogenous antioxidant enzymes after Vitamin E and C supplementation appear to be regulated by post-transcriptional modifications that are affected differently by age, exercise, and supplementation. These data suggest that antioxidant supplementation improves indices of oxidative stress associated with repetitive loading exercise and aging and improves the positive work output of muscles in aged rodents.


Asunto(s)
Envejecimiento/fisiología , Antioxidantes/farmacología , Ácido Ascórbico/farmacología , Músculo Esquelético/fisiología , Estrés Oxidativo/efectos de los fármacos , Oxidorreductasas/metabolismo , Esfuerzo Físico/fisiología , Vitamina E/farmacología , Animales , Daño del ADN/efectos de los fármacos , Glutatión/metabolismo , Disulfuro de Glutatión/metabolismo , Peróxido de Hidrógeno/metabolismo , Contracción Isométrica , Peroxidación de Lípido , Masculino , Músculo Esquelético/anatomía & histología , Músculo Esquelético/efectos de los fármacos , Tamaño de los Órganos , Oxidorreductasas/genética , ARN Mensajero/metabolismo , Ratas , Ratas Endogámicas F344
2.
J Gerontol A Biol Sci Med Sci ; 63(10): 1015-26, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18948551

RESUMEN

This study compares changes in the pro-oxidant production and buffering capacity in young and aged skeletal muscle after exposure to chronic repetitive loading (RL). The dorsiflexors from one limb of young and aged rats were loaded 3 times/week for 4.5 weeks using 80 maximal stretch-shortening contractions per session. RL increased H2O2 in tibialis anterior muscles of young and aged rats and decreased the ratio of reduced/oxidized glutathione and lipid peroxidation in aged but not young adult animals. Glutathione peroxidase (GPx) activity decreased whereas catalase activity increased with RL in muscles from young and aged rats. RL increased CuZn superoxide disumutase (SOD) and Mn SOD protein concentration and CuZn SOD activity in muscles from young but not aged animals. There were no changes in protein content for GPx-1 and catalase or messenger RNA for any of the enzymes studied. These data show that aging reduces the adaptive capacity of muscles to buffer increased pro-oxidants imposed by chronic RL.


Asunto(s)
Envejecimiento/fisiología , Catalasa/metabolismo , Glutatión Peroxidasa/metabolismo , Músculo Esquelético/enzimología , Superóxido Dismutasa/metabolismo , Análisis de Varianza , Animales , Western Blotting , Daño del ADN , Peroxidación de Lípido , Músculo Esquelético/fisiología , Oxidación-Reducción , Estrés Oxidativo , Ratas , Ratas Endogámicas F344 , Estrés Mecánico
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