Carbonylated proteins in aging and exercise: immunoblot approaches

被引:88
作者
Goto, S
Nakamura, A
Radak, Z
Nakamoto, H
Takahashi, R
Yasuda, K
Sakurai, Y
Ishii, N
机构
[1] Toho Univ, Sch Pharmaceut Sci, Dept Biochem, Funabashi, Chiba 2748510, Japan
[2] Hungarian Univ Phys Educ, H-1123 Budapest, Hungary
[3] Tokai Univ, Sch Med, Dept Mol Life Sci, Isehara, Kanagawa 2570811, Japan
关键词
protein oxidation; protein carbonyl; aging; exercise; nematode; vitellogenin;
D O I
10.1016/S0047-6374(98)00133-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Protein carbonyls were studied in aging and exercise by immunoblot followed by one- or two-dimensional polyacrylamide gel electrophoresis using antibodies against 2,4-dinitrophenylhydrazones. Proteins of rat kidneys exhibited significant age-related increase in the amount of carbonyl while those of the brain and liver did not. Major carbonylated proteins in the kidney included serum albumin. In nematodes in which protein carbonyls increased with age, one of the carbonylated proteins was identified as vitellogenin, an egg-yolk protein. A possible biological significance of this protein present in abundance even after egg-laying stages is discussed in terms of protection against oxidative stress. Exhaustive exercise induced significant increase in the carbonylation of selected but unidentified proteins in the lung. This oxidative stress might be caused by xanthine oxidase in this tissue and hypoxanthine derived from ATP-depleted muscles. Exercise at high altitude caused higher carbonylation of the skeletal muscle proteins, most notably a protein likely to be actin, than that at sea level but no significant difference was observed in lipid peroxidation. These studies emphasize the value of immunoblot analysis of tissue protein carbonyls in a variety of situations where oxidative stress is likely involved. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / 253
页数:9
相关论文
共 53 条
[1]   Effects of oxygen on protein carbonyl and aging in Caenorhabditis elegans mutants with long (age-1) and short (mev-1) life spans [J].
Adachi, H ;
Fujiwara, Y ;
Ishii, N .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1998, 53 (04) :B240-B244
[2]  
AMES BN, 1993, P NATL ACAD SCI USA, V90, P79515
[3]   GLYCATION OF ALBUMIN WITH AGING AND DIABETES IN RATS - CHANGES IN ITS RENAL HANDLING [J].
BAKALA, H ;
VERBEKE, P ;
PERICHON, M ;
CORMAN, B ;
SCHAEVERBEKE, J .
MECHANISMS OF AGEING AND DEVELOPMENT, 1995, 78 (01) :63-71
[4]   CHANGES IN PHYSICAL-FITNESS AND ALL-CAUSE MORTALITY - A PROSPECTIVE-STUDY OF HEALTHY AND UNHEALTHY MEN [J].
BLAIR, SN ;
KOHL, HW ;
BARLOW, CE ;
PAFFENBARGER, RS ;
GIBBONS, LW ;
MACERA, CA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (14) :1093-1098
[5]   Molecular and cellular adaptation of muscle in response to physical training [J].
Booth, FW ;
Tseng, BS ;
Flück, M ;
Carson, JA .
ACTA PHYSIOLOGICA SCANDINAVICA, 1998, 162 (03) :343-350
[6]   LOCALIZATION OF ALPHA-2U-GLOBULIN WITHIN PROTEIN DROPLETS OF MALE-RAT KIDNEY - IMMUNOHISTOCHEMISTRY USING PERFUSION-FIXED, GMA-EMBEDDED TISSUE-SECTIONS [J].
BURNETT, VL ;
SHORT, BG ;
SWENBERG, JA .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1989, 37 (06) :813-818
[7]   Proteins but not nucleic acids are molecular targets for the free radical attack during reoxygenation of rat hepatocytes [J].
Caraceni, P ;
DeMaria, N ;
Ryu, HS ;
Colantoni, A ;
Roberts, L ;
Maidt, ML ;
Pye, Q ;
Bernardi, M ;
VanThiel, DH ;
Floyd, RA .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (02) :339-344
[8]   FREE-RADICALS AND TISSUE-DAMAGE PRODUCED BY EXERCISE [J].
DAVIES, KJA ;
QUINTANILHA, AT ;
BROOKS, GA ;
PACKER, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 107 (04) :1198-1205
[9]  
DAVIES KJA, 1987, J BIOL CHEM, V262, P9902
[10]   CHEMISTRY AND BIOCHEMISTRY OF 4-HYDROXYNONENAL, MALONALDEHYDE AND RELATED ALDEHYDES [J].
ESTERBAUER, H ;
SCHAUR, RJ ;
ZOLLNER, H .
FREE RADICAL BIOLOGY AND MEDICINE, 1991, 11 (01) :81-128