Egzersiz Ãevrimiçi Dergi - Süleyman Demirel Ãniversitesi
Egzersiz Ãevrimiçi Dergi - Süleyman Demirel Ãniversitesi
Egzersiz Ãevrimiçi Dergi - Süleyman Demirel Ãniversitesi
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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