Current status of acrolein as a lipid peroxidation product

被引:259
作者
Uchida, K [1 ]
机构
[1] Nagoya Univ, Grad Sch Bioagr Sci, Lab Food & Biodynam, Nagoya, Aichi 4648601, Japan
关键词
D O I
10.1016/S1050-1738(99)00016-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is increasing evidence that aldehydes generated endogenously during lipid peroxidation contribute to the pathophysiologic effects associated with oxidative stress in cells and tissues. A number of reactive lipid aldehydes, such as 4-hydroxy-2-alkenals and malondialdehyde, have been implicated as causative agents in cytotoxic processes initiated by the exposure of biologic systems to oxidizing agents. Recently, acrolein (CH2 = CH - CHO), a ubiquitous pollutant in the environment, was identified as a product of lipid peroxidation reactions. The basis for this finding is an experimental approach that provides a measure of acrolein bound to lysine residues of protein. The identification of acrolein as an endogenous lipid-derived product suggests an examination of the possible role of this aldehyde as a mediator of oxidative damage in a variety of human diseases. (Trends Cardiovasc Med 1999;9:109-113). (C) 1999, Elsevier Science Inc.
引用
收藏
页码:109 / 113
页数:5
相关论文
共 33 条
[1]   Human neutrophils employ the myeloperoxidase-hydrogen peroxide-chloride system to convert hydroxy-amino acids into glycolaldehyde, 2-hydroxypropanal, and acrolein - A mechanism for the generation of highly reactive alpha-hydroxy and alpha,beta-unsaturated aldehydes by phagocytes at sites of inflammation [J].
Anderson, MM ;
Hazen, SL ;
Hsu, FF ;
Heinecke, JW .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (03) :424-432
[2]   Histochemical detection of 4-hydroxynonenal protein in Alzheimer amyloid [J].
Ando, Y ;
Brännström, T ;
Uchida, K ;
Nyhlin, N ;
Näsman, B ;
Suhr, O ;
Yamashita, T ;
Olsson, T ;
El Salhy, M ;
Uchino, M ;
Ando, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 156 (02) :172-176
[3]   Oxidative stress is found in amyloid deposits in systemic amyloidosis [J].
Ando, Y ;
Nyhlin, N ;
Suhr, O ;
Holmgren, G ;
Uchida, K ;
ElSahly, M ;
Yamashita, T ;
Terasaki, H ;
Nakamura, M ;
Uchino, M ;
Ando, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 232 (02) :497-502
[4]   Introduction of carbonyl groups into proteins by the lipid peroxidation product, malondialdehyde [J].
Burcham, PC ;
Kuhan, YT .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 220 (03) :996-1001
[5]   Protein-bound acrolein: A novel marker of oxidative stress in Alzheimer's disease [J].
Calingasan, NY ;
Uchida, K ;
Gibson, GE .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (02) :751-756
[6]   SYNTHESIS AND CHARACTERIZATION OF FLUORESCENT PRODUCTS DERIVED FROM MALONALDEHYDE AND AMINO ACIDS [J].
CHIO, KS ;
TAPPEL, AL .
BIOCHEMISTRY, 1969, 8 (07) :2821-+
[7]   IDENTIFICATION OF N-EPSILON-(2-PROPENAL)LYSINE AS A MAJOR URINARY METABOLITE OF MALONDIALDEHYDE [J].
DRAPER, HH ;
HADLEY, M ;
LISSEMORE, L ;
LAING, NM ;
COLE, PD .
LIPIDS, 1988, 23 (06) :626-628
[8]   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
[9]   REACTION OF CYSTEINE WITH ALPHA,BETA-UNSATURATED ALDEHYDES [J].
ESTERBAUER, H ;
ERTL, A ;
SCHOLZ, N .
TETRAHEDRON, 1976, 32 (02) :285-289
[10]  
ESTERBAUER H, 1975, Z NATURFORSCH C, V30, P466