Korać B, Buzadzić B, Saicić Z S, Radojicić R, Petrović V M
Institute for Biological Research, Belgrade, Yugoslavia.
J Environ Pathol Toxicol Oncol. 1998;17(3-4):305-11.
Skin protection against heat shock and the specificity in the organization of antioxidative defenses were examined in rats given oral antioxidative pretreatment with selenium (Se)-enriched yeast and vitamins E, C, and A for 15 days and then exposed to hyperthermia. The activity of antioxidative enzymes in the skin and the liver was monitored 1 hour and 3 hours after heat shock. Glutathione peroxidase (GSH-Px) activity was increased in the skin after heat shock in the groups supplemented with antioxidants, but not in the controls. In contrast, the activity of liver GSH-Px was increased only in the controls receiving antioxidants. Heat shock led to a decrease in liver superoxide dismutase (SOD) activity at 1 hour in the antioxidant-supplemented group, but this was unchanged in the liver of all other groups and in the skin. The activity of thioredoxin reductase (TR) in the skin was increased in the antioxidant supplemented group 1 hour after heat shock, whereas the hepatic thioredoxin reductase activity was decreased. The activities of catalase (CAT), glutathione reductase (GR), and glutathione-S-transferase (GST) were unaffected by either treatment. These results suggest that supplementation with antioxidants protects the skin against heat shock, especially with respect to the GSH-Px and TR activity. The different response of the skin in comparison with the liver probably reflects differences in organization and regulation of antioxidative defenses.
在给予富含硒(Se)的酵母以及维生素E、C和A进行口服抗氧化预处理15天,然后使其暴露于高温环境的大鼠中,研究了皮肤对热休克的保护作用以及抗氧化防御组织的特异性。在热休克后1小时和3小时监测皮肤和肝脏中抗氧化酶的活性。补充抗氧化剂的组在热休克后皮肤中的谷胱甘肽过氧化物酶(GSH-Px)活性增加,而对照组未增加。相反,仅在接受抗氧化剂的对照组中肝脏GSH-Px活性增加。在补充抗氧化剂的组中,热休克1小时后肝脏超氧化物歧化酶(SOD)活性降低,但在所有其他组的肝脏和皮肤中该活性未改变。热休克1小时后,补充抗氧化剂的组皮肤中的硫氧还蛋白还原酶(TR)活性增加,而肝脏中的硫氧还蛋白还原酶活性降低。过氧化氢酶(CAT)、谷胱甘肽还原酶(GR)和谷胱甘肽-S-转移酶(GST)的活性均不受任何一种处理的影响。这些结果表明,补充抗氧化剂可保护皮肤免受热休克,尤其是在GSH-Px和TR活性方面。与肝脏相比,皮肤的不同反应可能反映了抗氧化防御组织和调节的差异。