SKIN BURN INJURY AND OXIDATIVE STRESS IN LIVER AND LUNG TISSUES OF RABBIT MODELS

Citation
F. Sabeh et al., SKIN BURN INJURY AND OXIDATIVE STRESS IN LIVER AND LUNG TISSUES OF RABBIT MODELS, European journal of clinical chemistry and clinical biochemistry, 33(6), 1995, pp. 323-328
Citations number
44
Categorie Soggetti
Biology,"Chemistry Medicinal
ISSN journal
09394974
Volume
33
Issue
6
Year of publication
1995
Pages
323 - 328
Database
ISI
SICI code
0939-4974(1995)33:6<323:SBIAOS>2.0.ZU;2-X
Abstract
The effects of burn injury (30% of total body surface area) on the lev els of oxidized and reduced glutathione, malondialdehyde, and on the a ctivities of certain glutathione-dependent enzymes, have been determin ed in tissues of rabbit models. Thus, the malondialdehyde, glutathione (GSH), glutathione disulfide (GSSG) concentrations and the specific a ctivities of glutathione peroxidase, glutathione S-transferase, and gl utathione reductase were measured in liver and lung of 24-h burn rabbi t models and compared to the corresponding values in 24-h sham burn (m edicated, anesthetic/analgesic) rabbit models. It was found that the c oncentrations of malondialdehyde in liver and lung of burn models were increased by 17% and 29% respectively. Glutathione concentrations wer e decreased by 29% in liver and 13% in lung, and glutathione disulfide concentrations were increased by 35% in liver and 33% in lung, in bur n versus sham burn models. It was also found that the specific activit ies of glutathione peroxidase decreased significantly, resultant to bu rn injury, by an average of 35% and 27% in liver and lung, respectivel y. Burn injury also decreased glutathione S-transferase specific activ ities by 14% in liver and 23% in lung tissues. In contrast, glutathion e reductase specific activity was increased in liver tissues (22%), bu t was decreased (19%), as with the other enzymes studied, in lung tiss ues of burn models. Control model studies (no medication, no sham burn ) show that these effects of burn injury are additional to effects eli cited by medication associated with sham burn models. The data of this study are indicative of a major oxidative stress in liver and lung ti ssues due to burn injury at a remote site.