The role of oxygen and reduced oxygen species in nitric oxide-mediated cytotoxicity:: Studies in the yeast Saccharomyces cerevisiae model system
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作者:
Chiang, KT
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Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
Chiang, KT
[1
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Switzer, CH
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Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
Switzer, CH
[1
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Akali, KO
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Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
Akali, KO
[1
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Fukuto, JM
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Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
Fukuto, JM
[1
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机构:
[1] Univ Calif Los Angeles, Sch Med, Ctr Hlth Sci, Dept Pharmacol, Los Angeles, CA 90095 USA
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.