The role of oxygen and reduced oxygen species in nitric oxide-mediated cytotoxicity:: Studies in the yeast Saccharomyces cerevisiae model system

被引:9
作者
Chiang, KT [1 ]
Switzer, CH [1 ]
Akali, KO [1 ]
Fukuto, JM [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
关键词
nitric oxide; molecular oxygen; yeast; Saccharomyces cerevisiae; cytotoxicity; superoxide; hydrogen peroxide; superoxide dismutase; catalase; peroxynitrite; lipid peroxidation;
D O I
10.1006/taap.2000.8970
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The cytotoxicity of nitric oxide (NO) is well established, yet the mechanism(s) of its cytotoxicity is (are) still undefined and a matter of significant interest and speculation. Many of the previously proposed mechanisms for NO-mediated cytotoxicity involve interactions between NO and molecular oxygen (O-2) and/or O-2-derived species such as O-2(-) and H2O2. The yeast Saccharomyces cerevisiae represents a useful model system for evaluating the role of O-2 and O-2-derived species in NO-mediated cytotoxicity. This study examines the contribution of O-2 and O-2-derived species to NO-mediated cytotoxicity in the yeast S. cerevisiae. NO-mediated cytotoxicity was determined to be O-2-dependent. However, this O-2 dependence was only minimally due to the generation of O-2-derived species such as O-2(-) and/or H2O2. (C) 2000 Academic Press.
引用
收藏
页码:30 / 36
页数:7
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