Antioxidants as potential therapeutics for lung fibrosis

被引:108
作者
Day, Brian J. [1 ]
机构
[1] Natl Jewish Med & Res Ctr, Dept Med, Div Environm & Occupat Hlth Sci, Denver, CO 80206 USA
关键词
INDUCED PULMONARY-FIBROSIS; ORAL N-ACETYLCYSTEINE; GROWTH-FACTOR-BETA; CATALYTIC METALLOPORPHYRIN ANTIOXIDANT; LECITHINIZED-SUPEROXIDE-DISMUTASE; LIPOSOMAL ALPHA-TOCOPHEROL; EPITHELIAL LINING FLUID; ACUTE PARAQUAT TOXICITY; BILOBA EXTRACT EGB-761; NITRIC-OXIDE SYNTHASE;
D O I
10.1089/ars.2007.1916
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
Interstitial lung disease encompasses a large group of chronic lung disorders associated with excessive tissue remodeling, scarring, and fibrosis. The evidence of a redox imbalance in lung fibrosis is substantial, and the rationale for testing antioxidants as potential new therapeutics for lung fibrosis is appealing. Current animal models of lung fibrosis have clear involvement of ROS in their pathogenesis. New classes of antioxidant agents divided into catalytic antioxidant mimetics and antioxidant scavengers are being developed. The catalytic antioxidant class is based on endogenous antioxidant enzymes and includes the manganese-containing macrocyclics, porphyrins, salens, and the non-metal-containing nitroxides. The antioxidant scavenging class is based on endogenous antioxidant molecules and includes the vitamin E analogues, thiols, lazaroids, and polyphenolic agents. Numerous studies have shown oxidative stress to be associated with many interstitial lung diseases and that these agents are effective in attenuating fibroproliferative responses in the lung of animals and humans.
引用
收藏
页码:355 / 370
页数:16
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