A. Seven et al., Biochemical evaluation of oxidative stress in propylthiouracil treated hyperthyroid patients. Effects of vitamin c supplementation, CLIN CH L M, 36(10), 1998, pp. 767-770
In this study the impact of vitamin C supplementation on oxidative damage a
s assessed by thiobarbituric acid reactive substances and markers of antiox
idant status: namely Cu/Zn superoxide dismutase, glutathione peroxidase, gl
utathione reductase and glutathione were investigated in 24 hyper-thyroid p
atients under propylthiouracil therapy (3x100 mg/day) for five days and in
15 healthy controls. Ascorbic acid (1000 mg/day) was given as a supplement
for 1 month to both the patients and controls during the study period. Hepa
rinised blood samples were taken at the beginning and the end of one month
ascorbic acid supplementation.
Comparison of the hyperthyroid patients with the controls revealed higher l
ipid peroxidation (p<0.001), higher Cu/Zn superoxide dismutase activity (p<
0.001), higher glutathione level (<0.001) and lower glutathione reductase a
ctivity (p<0.001).
Vitamin C supplementation to hyperthyroid patients caused significant incre
ases in glutathione concentration (p<0.001) and glutathione peroxidase acti
vity (p<0.001), whereas there were significant decreases in glutathione red
uctase (p<0.001) and Cu/Zn superoxide dismutase activities (p<0.01). Thioba
rbituric acid reactive substances and thiobarbituric acid reactive substanc
es/glutathione ratio were significantly decreased (p<0.01).
Vitamin C supplementation to euthyroid controls caused significant increase
s in glutathione concentration (p<0.001) and glutathione peroxidase and Cu/
Zn superoxide dismutase activities (p<0.001), whereas there was a significa
nt decrease in glutathione reductase (p<0.001). The thiobarbituric acid rea
ctive substances/glutathione ratio was significantly decreased (p<0.05).
Our findings reveal the potentiation of antioxidant status and a relief in
oxidative stress in both propylthiouracil treated hyperthyroid patients and
controls in response to vitamin C supplementation.