Antioxidant systems in tissues of senescence accelerated mice

被引:36
作者
Bodyrev, AA [1 ]
Yuneva, MO
Sorokina, EV
Kramarenko, GG
Fedorova, TN
Konovalova, GG
Lankin, VZ
机构
[1] Moscow MV Lomonosov State Univ, Sch Biol, Dept Biochem, Moscow 119899, Russia
[2] Russian Acad Med Sci, Inst Neurol, Moscow 123367, Russia
[3] Cardiol Res Ctr, Moscow 121552, Russia
基金
俄罗斯基础研究基金会;
关键词
senescence accelerated mice; brain; antioxidant system;
D O I
10.1023/A:1012441215506
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
Significant decrease in the level of lipid antioxidants (measured from the kinetics of the induced chemiluminescence in brain homogenate) and of the hydrophilic antioxidant carnosine as well was observed in the brain of 14-16-month-old mice of SAMP1 line, which is characterized by accelerated accumulation of senile features, in comparison with the control line SAMR1. In the brain of SAMP1 animals the activity of cytosolic Cu/Zn-containing superoxide dismutase (SOD) was reduced, while the activity of membrane-bound Mn-SOD was at an extremely low level. The activity of glutathione-dependent enzymes (glutathione peroxidase, glutathione reductase, and glutathione transferase) did not differ ill the brain of SAMP1 and SAMR1 animals, and catalase activity was similarly low in both cases. At the same time, excess concentration of excitotoxic compounds, significantly exceeding that for the control line, was determined in the brain and blood of SAMP1 animals. The activity of glutathione enzymes in liver and heart as well as the activity of cytosolic Cu/Zn-SOD ill liver did not differ in the two studied lines, while the activity of erythrocyte glutathione peroxidase was slightly increased, and the activity of liver catalase and erythrocyte Cu/Zn-SOD was significantly decreased for SAMP1 compared with SAMR1. The results demonstrate that the accelerated ageing of SAMP1 animals is connected to a significant extent with the decreased efficiency of the systems utilizing reactive oxygen species (ROS) in tissues.
引用
收藏
页码:1157 / 1163
页数:7
相关论文
共 32 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   MAO inhibitors and oxidant stress in aging brain tissue [J].
Alper, G ;
Girgin, FK ;
Ozgönül, M ;
Mentes, G ;
Ersöz, B .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 1999, 9 (03) :247-252
[3]   ERYTHROCYTE GLUTATHIONE REDUCTASE [J].
BEUTLER, E ;
YEH, MKY .
BLOOD, 1963, 21 (05) :573-&
[4]   Carnosine protects against excitotoxic cell death independently of effects on reactive oxygen species [J].
Boldyrev, A ;
Song, R ;
Lawrence, D ;
Carpenter, DO .
NEUROSCIENCE, 1999, 94 (02) :571-577
[5]  
Boldyrev A., 2000, B EKSP BIOL MED, V130, P244
[6]  
BOLDYREV A, 1995, COMP BIOCH PHYSL B, V112, P546
[7]  
BULYGINA E, 1999, J ANTI-AGING MED, V2, P45
[8]   Hydrogen peroxide-mediated Cu,Zn-superoxide dismutase fragmentation: protection by carnosine, homocarnosine and anserine [J].
Choi, SY ;
Kwon, HY ;
Kwon, OB ;
Kang, JH .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1472 (03) :651-657
[9]  
Fedorova TN, 1999, BIOCHEMISTRY-MOSCOW+, V64, P75
[10]  
HALLIWELL B, 1999, FREE RADICAL BIO MED, P135