Down regulation of superoxide dismutases and glutathione peroxidase by reactive oxygen and nitrogen species

被引:53
作者
Fujii, J [1 ]
Taniguchi, N [1 ]
机构
[1] Osaka Univ, Sch Med, Dept Biochem, Suita, Osaka 5650871, Japan
关键词
apoptosis; diabetes; glycation; peroxide;
D O I
10.1080/10715769900300861
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
The levels of antioxidative enzymes are regulated by gene expressions as well as by post-translational modifications. Although their functions are to scavenge reactive oxygen (ROS) and nitrogen species (RNS), they may also be targets of various oxidants. When ROS and RNS modify the functions of antioxidative enzymes, especially glutathione peroxidase, they may induce apoptotic cell death in susceptible cells. It is conceivable, therefore, that at least a part of the apoptotic pathways mediated by ROS and RNS may be associated with modification of the redox regulation of cellular functions due to elevations of such substances. In this article we review recent findings about the effects of various oxidative conditions associated with alteration of these antioxidative enzymes and the concomitant cellular damage induced.
引用
收藏
页码:301 / 308
页数:8
相关论文
共 42 条
[1]   IMMUNOHISTOCHEMICAL EXPRESSION OF MANGANESE SUPEROXIDE-DISMUTASE IN HEPATOCELLULAR-CARCINOMA, USING A SPECIFIC MONOCLONAL-ANTIBODY [J].
AIDA, Y ;
MAEYAMA, S ;
TAKAKUWA, T ;
UCHIKOSHI, T ;
ENDO, Y ;
SUZUKI, K ;
TANIGUCHI, N .
JOURNAL OF GASTROENTEROLOGY, 1994, 29 (04) :443-449
[2]  
AMSTAD P, 1994, J BIOL CHEM, V269, P1606
[3]  
ARAI K, 1987, J BIOL CHEM, V262, P16969
[4]   Mitochondrial phospholipid hydroperoxide glutathione peroxidase plays a major role in preventing oxidative injury to cells [J].
Arai, M ;
Imai, H ;
Koumura, T ;
Yoshida, M ;
Emoto, K ;
Umeda, M ;
Chiba, N ;
Nakagawa, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (08) :4924-4933
[5]   INACTIVATION OF GLUTATHIONE-PEROXIDASE BY NITRIC-OXIDE - IMPLICATION FOR CYTOTOXICITY [J].
ASAHI, M ;
FUJII, J ;
SUZUKI, K ;
SEO, HG ;
KUZUYA, T ;
HORI, M ;
TADA, M ;
FUJII, S ;
TANIGUCHI, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (36) :21035-21039
[6]   The oxidation of selenocysteine is involved in the inactivation of glutathione peroxidase by nitric oxide donor [J].
Asahi, M ;
Fujii, J ;
Takao, T ;
Kuzuya, T ;
Hori, M ;
Shimonishi, Y ;
Taniguchi, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19152-19157
[7]   SUPEROXIDE-DISMUTASE-1 WITH MUTATIONS LINKED TO FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS POSSESSES SIGNIFICANT ACTIVITY [J].
BORCHELT, DR ;
LEE, MK ;
SLUNT, HS ;
GUARNIERI, M ;
XU, ZS ;
WONG, PC ;
BROWN, RH ;
PRICE, DL ;
SISODIA, SS ;
CLEVELAND, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :8292-8296
[8]   SOD1 aggregates in ALS: Cause, correlate or consequence? [J].
Brown, RH .
NATURE MEDICINE, 1998, 4 (12) :1362-1364
[9]   Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1 [J].
Bruijn, LI ;
Houseweart, MK ;
Kato, S ;
Anderson, KL ;
Anderson, SD ;
Ohama, E ;
Reaume, AG ;
Scott, RW ;
Cleveland, DW .
SCIENCE, 1998, 281 (5384) :1851-1854
[10]  
CHAE HZ, 1994, BIOFACTORS, V4, P177