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Attenuation of age-dependent oxidative damage to DNA and protein in brainstem of Tg Cu/Zn SOD mice
被引:36
作者:
Cardozo-Pelaez, F
Song, S
Parthasarathy, A
Epstein, CJ
Sanchez-Ramos, J
机构:
[1] Univ S Florida, James Haley VA Hosp, Dept Neurol, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Neurol, Tampa, FL 33620 USA
[3] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
关键词:
aging;
8-hydroxy-2 '-deoxyguanosine;
oxidative DNA damage;
protein oxidation;
Parkinson's disease;
superoxide dismutase;
transgenic mice;
D O I:
10.1016/S0197-4580(98)00067-0
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
Age-dependent accumulation of oxidative DNA and protein damage in brainstem and striatum was assessed in normal and transgenic (tg) mice which overexpress human Cu/Zn superoxide dismutase (h-SOD1). A marker of oxidative DNA damage, 8-hydroxy-2'-deoxyguanosine (oxo(8)dG), was measured at 3, 12, and 18 months of age in control and tg mice. Cu/Zn SOD, but not MnSOD, activities in brainstems and striata from tg mice were increased compared to controls at all ages. At 18 months, oxo8dG levels were increased by 58% in brainstem and by 21% in striatum of control mice. In the tg mice, brainstem and striatal oxo8dG levels were increased to a lesser extent than in the corresponding controls. Protein oxidation (carbonyl content), was increased by 59% at 18 months in control brainstem, but not in striatum, and the increase was significantly attenuated in the tg mice. In summary, oxidative damage to DNA and protein increased with age in brainstem land to a lesser extent in striatum), and augmented Cu/Zn SOD activity modified the extent of DNA and protein damage. (C) 1998 Elsevier Science Inc.
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页码:311 / 316
页数:6
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