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Egzersiz Çevrimiçi Dergi - Süleyman Demirel Üniversitesi

Egzersiz Çevrimiçi Dergi - Süleyman Demirel Üniversitesi

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Methods<br />

Plasma methaemoglobin concentrations<br />

were analyzed immediately after the blood samples<br />

are collected aand its level was measured<br />

spectrophotometrically according to Fairbanks<br />

and Klee (1987). MDA was estimated according<br />

to method of Draper and Hardley (1990) which<br />

is based on the coupling MDA with thiobarbituric<br />

acid. Plasma antioxidant activity (AOA) was<br />

measured according to method of Koracevic et<br />

al. (2001). Briefly, a standardised solution of Fe–<br />

EDTA complex reacts with hydrogen peroxide by<br />

a Fenton-type reaction, leading to the formation<br />

of hydroxyl radicals. Nitric oxide metabolites (nitrates+<br />

nitrites, NO×) were assayed in plasma<br />

by colorimetric method of Griess (Miranda et al.<br />

2001). Total protein, total cholesterol, glucose<br />

and triglycerides levels were measured using<br />

the commercially available assay kits (TECO Diagnostics,<br />

California, USA). Statistical analyses<br />

of data from the experiment were analyzed with<br />

SPSS statistical software (SPSS for Windows;<br />

Release 10.0.1 Standart Version) using paired t<br />

test.<br />

Results<br />

For all subjects, MDA and glocose concentrations<br />

increased after exercise(p

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