Effects of mitochondrial respiratory stimulation on membrane lipids and proteins: an electron paramagnetic resonance investigation

被引:35
作者
Gabbita, SP
Subramaniam, R
Allouch, F
Carney, JM
Butterfield, DA [1 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[2] Univ Kentucky, Grad Ctr Toxicol, Lexington, KY USA
[3] Univ Kentucky, Ctr Membrane Sci, Lexington, KY 40506 USA
[4] Univ Kentucky, Dept Pharmacol, Lexington, KY USA
[5] Centaur Pharmaceut Inc, Sunnyvale, CA USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1998年 / 1372卷 / 02期
关键词
brain; mitochondrion; electron paramagnetic resonance; protein oxidation; lipid peroxidation; MAL-6; 5-nitroxyl stearate;
D O I
10.1016/S0005-2736(98)00040-6
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
Previous studies have implicated mitochondria-derived reactive oxygen species (ROS) in both the aging process and age-related diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Parkinson's disease etc. The current study, utilizing electron paramagnetic resonance (EPR) spectrometry, was designed to determine if mitochondrial respiratory stimulation, under state 4 conditions, caused extensive oxidative modifications to membrane cytoskeletal proteins and lipids in the brain. A mixed population of cortical synaptosomes and mitochondria, prepared by centrifugation techniques using rat brain cortex from adult (4-6 months) female Brown Norway rat brains, were labeled with the lipid-specific spin probe, 5-nitroxyl stearate (5-NS). Stimulation of the mitochondrial electron transport chain was accomplished using 20 mM succinate at 25 degrees C for 3 h. Mitochondrially derived free radicals, when reacted with the paramagnetic center of the spin probe, result in a loss of paramagnetism resulting in loss of intensity. A significant lowering (23%, P < 0.0001) in the signal amplitude (B-o) of 5-NS, indicative of generation of oxyradicals, was found. The order parameter, an inverse EPR-measure of membrane fluidity of the 5-NS spin labeled mitochondrial and synaptosomal membranes, also decreased following mitochondrial respiratory stimulation (P<0.005). Changes in the physical state of cytoskeletal and transmembrane proteins due to succinate oxidation were measured using MAL-6 (2,2,6,6,-tetramethyl-4 maleimidopiperdin-1-oxyl), a thiol-specific nitroxide spin label, The ratio of the amplitudes of the weakly to strongly immobilized spin label reaction sites (W/S ratio) in the low-field region of the spectrum was used to determine any alteration in protein conformation. Previous studies in our laboratory have established that increased protein oxidation is associated with a decreased W/S ratio. In the current study, our results indicated significant lowering of the W/S ratio in cortex (30%, P < 0.0001) upon stimulation of the mitochondria with 20 mM succinate. Thus, we conclude that respiratory stimulation of mitochondria, due to a hypermetabolic stress with succinate, caused significant oxidative modifications of cortical membrane lipids and proteins. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 173
页数:11
相关论文
共 48 条
[1]   OXIDATIVE DAMAGE TO DNA - RELATION TO SPECIES METABOLIC-RATE AND LIFE-SPAN [J].
ADELMAN, R ;
SAUL, RL ;
AMES, BN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2706-2708
[2]   LOW MITOCHONDRIAL FREE-RADICAL PRODUCTION PER UNIT O-2 CONSUMPTION CAN EXPLAIN THE SIMULTANEOUS PRESENCE OF HIGH LONGEVITY AND HIGH AEROBIC METABOLIC-RATE IN BIRDS [J].
BARJA, G ;
CADENAS, S ;
ROJAS, C ;
PEREZCAMPO, R ;
LOPEZTORRES, M .
FREE RADICAL RESEARCH, 1994, 21 (05) :317-327
[3]  
BEAL MF, 1994, NEUROBIOL AGING, V15, pS171
[4]   REDUCTION AND DESTRUCTION RATES OF NITROXIDE SPIN PROBES [J].
BELKIN, S ;
MEHLHORN, RJ ;
HIDEG, K ;
HANKOVSKY, O ;
PACKER, L .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 256 (01) :232-243
[5]  
BOVERIS A, 1984, METHOD ENZYMOL, V105, P429
[6]   SUPEROXIDE-DISMUTASE ACTIVITY, OXIDATIVE DAMAGE, AND MITOCHONDRIAL ENERGY-METABOLISM IN FAMILIAL AND SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS [J].
BOWLING, AC ;
SCHULZ, JB ;
BROWN, RH ;
BEAL, MF .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (06) :2322-2325
[7]   OXIDATIVE DAMAGE AND MITOCHONDRIAL DYSFUNCTION IN NEURODEGENERATIVE DISEASES [J].
BROWNE, SE ;
BEAL, MF .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1994, 22 (04) :1002-1006
[8]  
Butterfield D.A., 1997, ADV CELL AGING GERON, V2, P161
[9]   Free radical oxidation of brain proteins in accelerated senescence and its modulation by N-tert-butyl-alpha-phenylnitrone [J].
Butterfield, DA ;
Howard, BJ ;
Yatin, S ;
Allen, KL ;
Carney, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :674-678
[10]   beta-Amyloid-associated free radical oxidative stress and neurotoxicity: Implications for Alzheimer's disease [J].
Butterfield, DA .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (05) :495-506