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Aquatic invertebrates use antioxidant systems to endure intertidal environments, where temperature, oxygen availability and radiation incidence vary greatly. The upregulation of antioxidants during oxygen-limiting conditions, such as intertidal aerial exposure (AE), is known as preparation for oxidative stress (POS). Preparation for oxidative stress has been commonly reported for animals exposed to hypoxia in the lab, but few studies have investigated it under ecologically relevant natural settings. Here, we studied metabolic enzymes, antioxidants, and oxidative stress markers in Brachidontes solisianus mussels exposed to a natural tidal cycle in a rocky beach in Southern Brazil. Animals were collected at 6 time-points throughout the tidal cycle: after 2 h of AE; then after 1 h, 3 h, and 7 h of immersion; followed by 0.5 h and 4 h of AE. The activities of malate dehydrogenase, isocitrate dehydrogenase, and pyruvate kinase were unaffected by aerial exposure. Similarly, the acitivities of enzymes of the antioxidant system, catalase, glutathione transferase, glutathione reductase, and glucose 6-phosphate dehydrogenase did not change significantly throughout the tidal cycle. In contrast, total and reduced glutathione levels significantly increased at 4 h AE by 47% and 64%, respectively, compared with those in submerged mussels (1 h, 3 h, and 7 h immersion groups combined). Lipid peroxidation and carbonyl protein levels significantly increased after 4 h of AE compared with those in mussels underwater for 7 h. Our results indicate the occurrence of POS in B. solisianus mussels exposed to air under natural conditions during tidal cycles.

Crocodilians and other diving vertebrates experience hypoperfusion and hypoxia of several internal organs during long dives. At the end of a dive, reperfusion of aerated blood may cause a physiologically relevant oxidative stress. In this study, we analyzed selected markers of oxidative stress in eight organs of normoxic Paraguayan caiman (Caiman yacare) captured in the Brazilian Pantanal wetlands during the winter of 2001 (six mature-adult males and eight young-adult males; AD-1 and YA-1 groups, respectively), and during the summer of 2002 (six young-adult males (YA-2 group), ten hatchlings and five embryos). Lipid peroxidation products determined by three different assays were generally highest in brain, liver and kidney (in comparison with all other organs), and lowest in white muscles from the tail and hind legs. Liver and kidney showed the highest levels of carbonyl protein, while brain showed low levels. Intermediate levels of oxidative stress markers were mostly found in the heart ventricles and lung. Differences in oxidative stress markers between AD-1 and YA-1 were organ-specific, showing no age-related correlation. However, most oxidative stress markers in YA-2 organs were either higher than (by 1.4- to 3.7-fold) or not significantly different from respective values in hatchlings organs. This pattern (hatchlings versus young-adults) was confirmed using correlation analysis of individual caiman size versus levels of oxidative damage markers in four organs. The higher level of oxidative stress markers in young-adults possibly relates to the fast growth rate (and thus, increased oxidative metabolic rate) of C. yacare in the first years of life. Differences in oxidative stress markers between YA-1 and YA-2 were also observed and were ascribed to seasonal changes in free radical metabolism. These results in normoxic C. yacare represent the first step towards understanding the age-related physiological oxidative stress of a diving reptile from a seasonally changing wetland environment.

To assess the effect of 950 MHz ultra-high-frequency electromagnetic radiation (UHF EMR) on biomarkers of oxidative damage, as well as to verify the concentration of unsaturated fatty acids (UFA) and the expression of the catalase in the livers of rats of different ages.Twelve rats were equally divided into two groups as controls (CR) and exposed (ER), for each age (0, 6, 15 and 30 days). Radiation exposure lasted half an hour per day for up to 51 days (21 days of gestation and 6, 15 or 30 days of life outside the womb). The specific absorption rate (SAR) ranged from 1.3-1.0 W/kg. The damage to lipids, proteins and DNA was verified by thiobarbituric acid reactive substances (TBARS), protein carbonyls and comets, respectively. UFA were determined by gas chromatography with a flame ionization detector. The expression of catalase was by Western blotting.The neonates had low levels of TBARS and concentrations of UFA after exposure. There was no age difference in the accumulation of protein carbonyls for any age. The DNA damage of ER 15 or 30 days was different. The exposed neonates exhibited lower expression of catalase.950 MHz UHF EMR does not cause oxidative stress (OS), and it is not genotoxic to the livers of neonates or those of 6 and 15 day old rats, but it changes the concentrations of polyunsaturated fatty acid (PUFA) in neonates. For rats of 30 days, no OS, but it is genotoxic to the livers of ER to total body irradiation.