In vivo ozone exposure induces antioxidant/stress-related responses in murine lung and skin

被引:105
作者
Valacchi, G
Pagnin, E
Corbacho, AM
Olano, E
Davis, PA
Packer, L
Cross, CE
机构
[1] CCRBM, Dept Internal Med, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[3] Univ So Calif, Sch Pharm, Los Angeles, CA 90089 USA
关键词
ozone; heme oxygenase; heat stress proteins; lipid peroxidation; cyclooxygenase; 2; keratinocytes; nuclear factor kappa B; proliferating cell nuclear antigen; free radicals;
D O I
10.1016/j.freeradbiomed.2003.12.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung and skin are the organs directly exposed to environmental pollution. Ozone (03) is a toxic, oxidant air pollutant, and exposure has been shown to induce antioxidant depletion as well as oxidation of lipids and proteins within the outermost skin layer (stratum corneum) and the lung respiratory tract lining fluids (RTLFs). To further define skin and lung responses to 03 exposure, SKH-1 hairless mice were exposed to either 0.8 ppm of O-3 (a level occasionally reached in very polluted areas) or ambient air 6 h/day for 6 consecutive days. O-3 exposure resulted in the depletion of alpha-tocopherol in lung and plasma and induction in both skin and lung of heme oxygenase 1, cyclooxygenase 2, and proliferating cell nuclear antigen. O-3-exposed animals showed a similar extent of upregulation of COX-2 and PCNA in lung and skin, whereas HO-1 was more responsive in skin than in lung (7-fold induction vs. 2-fold induction). In addition to these measures of response to oxidative stress, O(3-)exposure led to the activation of nuclear factor kappaB measured as IkappaBalpha phosphorylation in both tissues. We conclude that in this model, O-3 at high pollutant levels is able to affect both lung and skin biology, inducing depletion of alpha-tocopherol and inducing stress-related responses in both skin epidermis and respiratory tract epithelium. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:673 / 681
页数:9
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