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1.
J Sports Med Phys Fitness ; 48(4): 522-9, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18997658

RESUMEN

AIM: Total antioxidant capacity (TAC) is an essential parameter to watch over defense system of athletes exposed to an oxidant stress during intensive periods of training. To control this parameter throughout the training period, repetitive biological samples are required. The TAC is usually investigated in venous blood which needs invasive withdrawings. Thus, we proposed to find alternatives to venous blood analysis by venepuncture, which is invasive, stressful and not allow a regular follow-up on athletes during annual training season. METHODS: We measured capillary and salivary TAC in 65 physically active subjects at rest and compared them to the venous TAC. We followed the evolution of venous and salivary TAC in 7 triathletes throughout an annual training period (March and June) corresponding to two different types of training. RESULTS: There was a good correlation between plasma venous and capillary TAC values (r=0.77; P<0.0001), but salivary TAC were significantly lower than the plasma ones and did not correlate. Venous and saliva TAC of triathletes were significantly higher in March compared to June. The variations of plasma and salivary TAC between the two periods of training were correlated (r=0.96; P<0.01). CONCLUSION: The capillary sampling can replace the venous one for TAC evaluation in routine assays for the follow-up of athletes. Even if saliva TAC did not reflect plasma TAC, it could be used in the follow-up of athletes since a strong correlation is found between the variation of saliva and plasma TAC during the training season.


Asunto(s)
Antioxidantes/metabolismo , Ácido Peroxinitroso/metabolismo , Resistencia Física/fisiología , Saliva/metabolismo , Deportes/fisiología , Capilares , Femenino , Estudios de Seguimiento , Humanos , Masculino , Ácido Peroxinitroso/sangre , Valores de Referencia , Descanso/fisiología , Venas , Adulto Joven
2.
Eur J Appl Physiol ; 89(1): 14-20, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12627300

RESUMEN

It has been well demonstrated that the principal factor responsible for oxidative damage during exercise is the increase in oxygen consumption. However, other theoretical factors (acidosis, catecholamine autoxidation, ischemia-reperfusion syndrome, etc.) that are known to induce, in vitro, oxidative damage may also be operative during short-term supramaximal anaerobic exercise. Therefore, we hypothesized that short-term supramaximal anaerobic exercise (30-s Wingate test) could induce an oxidative stress. Lipid peroxidation markers [serum lipid radical production detected by electron spin resonance (ESR) spectroscopy and plasma malondialdehyde (MDA) levels detected by the thiobarbituric acid reactive substances (TBARS) method], as well as erythrocyte antioxidant enzyme activities [glutathione peroxidase (GPx), superoxide dismutase (SOD)] and erythrocyte glutathione (GSH) levels, were measured at rest, after the Wingate test and during the 40 min of recovery. The recovery of exercise was associated with a significant increase (x2.7) in lipid radical production detected by ESR spectroscopy, as well as with changes in the erythrocyte GSH level (-13.6%) and SOD activity (-11.7%). The paradoxical decrease in plasma TBARS (-23.7%) which was correlated with the peak power developed during the Wingate test ( r=-0.7), strongly suggests that such exercise stimulates the elimination of MDA. In conclusion, this study demonstrates that short-term supramaximal anaerobic exercise induces an oxidative stress and that the plasma TBARS level is not a suitable marker during this type of exercise.


Asunto(s)
Eritrocitos/metabolismo , Tolerancia al Ejercicio/fisiología , Peroxidación de Lípido/fisiología , Lípidos/sangre , Malondialdehído/sangre , Malondialdehído/metabolismo , Estrés Oxidativo/fisiología , Adulto , Anaerobiosis/fisiología , Antioxidantes/metabolismo , Biomarcadores/sangre , Activación Enzimática , Prueba de Esfuerzo , Glutatión/sangre , Glutatión/metabolismo , Glutatión Peroxidasa/sangre , Glutatión Peroxidasa/metabolismo , Humanos , Masculino , Superóxido Dismutasa/sangre , Superóxido Dismutasa/metabolismo
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