Using MT-/- mice to study metallothionein and oxidative stress

被引:40
作者
Conrad, CC
Grabowski, DT
Walter, CA
Sabia, M
Richardson, A
机构
[1] S Texas Vet Hlth Care Syst, Geriatr Res Educ & Clin Ctr, San Antonio, TX 78284 USA
[2] Univ N Texas, Hlth Sci Ctr, Dept Mol Biol & Immunol, Ft Worth, TX 76107 USA
[3] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78285 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Physiol, San Antonio, TX 78285 USA
基金
美国国家卫生研究院;
关键词
metallothionein; knockout mice; liver; DNA oxidation; lipid peroxidation; protein oxidation; free radicals;
D O I
10.1016/S0891-5849(99)00263-4
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
Mice with null mutations for metallothionein genes MT-1 and MT-2 were used to study the role that metallothionein plays in protecting cellular targets in vivo from oxidative stress. Wild-type (MT+/+) and MT-null (MT-/-) mice were treated with either saline or zinc and exposed to two types of oxidative stress: gamma-irradiation or 2-nitropropane. There was no alteration in the antioxidant defense system (superoxide dismutase, catalase, or glutathione peroxidase and glutathione levels) to compensate for the lack of the metallothionein in the MT-/- mice. The amount of oxidative damage to liver DNA, lipids, and proteins were similar for the MT-/- and MT+/+ mice even though the levels of metallothionein in the livers of the saline- or zinc-pretreated MT+/+ mice were 5- to 100-fold greater than found in the MT-/- mice. To determine if metallothionein can protect mice from the lethal effects of ionizing radiation, the mean survivals of MT-/- and MT+/+ mice exposed to whole body gamma-irradiation were measured and found to be similar. However, the mean survival increased significantly after zinc pretreatment for both the MT-/- and MT+/+ mice. These results demonstrate that tissue levels of metallothionein do not protect mice in vivo against oxidative stress. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:447 / 462
页数:16
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