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Acta Physiologica 2007; Volume 191, Supplement 658
Joint Meeting of The Slovak Physiological Society, The Physiological Society and The Federation of European Physiological Societies
9/11/2007-9/14/2007
Bratislava, Slovakia
GLOBAL ISCHAEMIC BRAIN INJURY IN RATS: A TIME COURSE OF OXIDATIVE STRESS IN PLASMA
Abstract number: OF18-69
Lehotsky1 J., Sivonova1 M., Kaplan1 P., Durackova1 Z., Drgova1 A., Tatarkova1 Z., Pavlikova1 M., Urban1 P., Dobrota1 D.
1Dept. of Medical Biochemistry, Comenius University, Jessenius Faculty of Medicine, Martin, Slovakia; Dept. of Medical Chemistry, Biochemistry and Clinical Chemistry, Comenius University, Faculty of Medicine Bratislava, Slovakia [email protected]
Aims:
Free radicals play an important role in the pathogenesis of brain injury. The purpose of this study was to evaluate the potential relationship between the peripheral oxidative stress and ischaemia/reperfusion (I/R)-induced brain.
Methods:
We quantified: (1) lymphocyte DNA damage, (2) plasma antioxidant potential and (3) uric acid levels as well as (4) a time course of peripheral oxidative stress on reperfusion period after ischaemic attack.
Results:
We observed that 15 min of ischaemia significantly increased lymphocyte DNA damage. In parallel, antioxidant potential was significantly elevated after 15 min of ischaemia, as well as after 3 h of reperfusion, when compared to pre-operative levels. A significant correlation can be found between the plasma uric acid and antioxidant potential of plasma after brain I/R. Evidence is presented by in vitro experiments that uric acid is the main component of increased antioxidant capacity seen in early reperfusion period. A significant decrease in total antioxidant potential was observed at 72 h reperfusion and this fall is correlated with the decrease of uric acid level.
Conclusions:
These results indicate a close time dependent association between brain I/R-associated oxidative stress and peripheral antioxidant defence status and/or oxidative stress in animal experiments. The study also suggests for uric acid and antioxidant capacity as an independent clinical outcome predictors in stroke patients.
Supported by: VEGA 3380/06, MVTS COST B30.
To cite this abstract, please use the following information:
Acta Physiologica 2007; Volume 191, Supplement 658 :OF18-69