Lipid peroxidation and the antioxidant system of the heart, liver, and brain are studied in adult male Wistar rats with high and low resistance to hypoxia tested by "raising" to an altitude of 11.5 km and in intact outbred rats. These parameters are found to be the same in the brain of low-and high-resistance rats, while the brain content of lipid peroxidation products is higher in both groups of Wistar rats compared with outbred rats. The heart and liver parameters are coupled to the resistance to hypoxia. Antioxidant activity prevails over lipid peroxidation in the hearts and livers of high-resistance rats, confirming that oxidation plays a major role in the damaging and lethal effects of acute hypoxia.Key Words: lipid peroxidation; antioxidant system; hypoxia; low resistance; high resistance Hypoxic and reoxygenation damage are known to be associated with diminished activity of the antioxidant system (AOS) [12,13] and with activation of lipid peroxidation (LPO) [2,12,13]. Adaptation to hypoxia leads to changes in the activity of tissue AOS [3,8] and in the content of LPO products [6,7]. At the same time, species-specific and intraspecies (individual) variations of resistance to hypoxia have been demonstrated [1]. It can be assumed that the activity of tissue AOS and LPO is different in animals with different degrees of resistance to hypoxia. Meanwhile, few studies have been performed on rat blood [10], while the state of LPO and AOS in the vital organs in animals differing in their resistance to hypoxia has not been assessed. Our purpose was to investigate the LPO content and AOS activity in the brain, heart, and liver of rats with low and high resistance to hypoxia.
MATERIALS AND METHODSExperiments were performed on 20 Wistar rats and 10 outbred rats in winter. Wistar rats were tested by "being raised" them to an altitude of 11.5 km during 1 min (twice, three weeks apart) [1]. The survival period of high-resistance (HR) rats was 5.3-fold longer in comparison with low-resistance (LR) rats (450+42 vs.86+5 sec, respectively, p<0.01). Three weeks after the repeat test, the brain, heart, and liver were rapidly excised under thiopental anesthesia after a 2.5-min perfusion with cold (0-4~ normal saline. The organs were homogenized and homogenates prepared from organs of 2-3 animals were pooled in one sample. There were 4-5 samples in each group of rats. Lipids were extracted from the homogenates as described elsewhere [11] with a chloroform-ethanol mixture (1:2) in the presence of 10 -s M ionol. Light absorbance (D) of lipids dissolved in hexane was measured in a Hewlett-Packard spectrophotometer at 215 nm (total lipids), 232 nm (diene conjugates), and 275 nm (ketotriene conjugates). All parameters were calculated per mg lipid. The oxidation indexes D232/215 and D275/215 reflecting the proportion of lipids oxi-0007..4888/96/0001-0022515.00 9Plenum Publishing Corporation