Pb2+ promotes lipid oxidation and alterations in membrane physical properties

被引:101
作者
Adonaylo, VN [1 ]
Oteiza, PI [1 ]
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, CONICET, Inst Quim & Fisicoquim Biol, RA-1113 Buenos Aires, DF, Argentina
关键词
lead; lipid oxidation; iron; free radicals; phase separation;
D O I
10.1016/S0300-483X(98)00134-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Experimental evidence suggests that cellular damage mediated by oxidants could be involved in the pathology associated with lead (Pb) toxicity. We investigated the effect of Pb2+ on lipid oxidation in liposomes using different initiators. In the presence of Fe2+ Pb2+ (12.5-200 mu M) Stimulated lipid oxidation in phosphatidylcholine:phosphatidylserine-containing liposomes, measured as 2-thiobarbituric acid-reactive substances (TBARS) and conjugated dienes. This stimulatory effect depended on the presence of membrane negative charges and on bilayer integrity. Pb2+ did not stimulate TEARS formation in the presence of 25 mM 2,2'-azo-bis (2,4 dimethylvaleronitrile (AMVN) and 2,2' azobis (2-amidinopropane) (AAPH). Pb2+ significantly stimulated TEARS production and NADH oxidation in the presence of photoactivated rose Bengal. The use of specific inhibitors indicated that several reactive oxygen species were involved in the pro-oxidant action of Pb2+. Pb2+ (12.5-200 mu M) caused membrane lateral phase separation and this effect was positively correlated with its capacity to stimulate Fe2+ and rose Bengal-initiated TEARS production. Pb2+ could bind to the membrane and act to stimulate lipid oxidation by causing changes in membrane physical properties. Through this mechanism Pb2+ would favor the propagation of lipid oxidation. By causing lateral phase separation and/or by increasing lipid oxidation rates, Pb2+ could be cytotoxic by altering membrane-related processes. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:19 / 32
页数:14
相关论文
共 28 条
[1]   THE MECHANISM OF INITIATION OF LIPID-PEROXIDATION - EVIDENCE AGAINST A REQUIREMENT FOR AN IRON(II) IRON(III) COMPLEX [J].
ARUOMA, OI ;
HALLIWELL, B ;
LAUGHTON, MJ ;
QUINLAN, GJ ;
GUTTERIDGE, JMC .
BIOCHEMICAL JOURNAL, 1989, 258 (02) :617-620
[2]  
Bechara EJH, 1993, QUIM NOVA, V16, P385
[3]  
BIELSKY BHJ, 1983, J BIOL CHEM, V253, P4759
[4]   STUDIES ON PEROXIDATION OF ARACHIDONIC-ACID IN DIFFERENT LIPOSOMES BELOW AND ABOVE PHASE-TRANSITION TEMPERATURE [J].
CERVATO, G ;
VIANI, P ;
MASSERINI, M ;
DIIORIO, C ;
CESTARO, B .
CHEMISTRY AND PHYSICS OF LIPIDS, 1988, 49 (1-2) :135-139
[5]   MICRODETERMINATION OF PHOSPHORUS [J].
CHEN, PS ;
TORIBARA, TY ;
WARNER, H .
ANALYTICAL CHEMISTRY, 1956, 28 (11) :1756-1758
[6]   FE2+-INDUCED LIPID-PEROXIDATION KINETICS IN LIPOSOMES - THE ROLE OF SURFACE FE2+ CONCENTRATION IN SWITCHING THE REACTION FROM ACCELERATION TO DECAY [J].
DRIOMINA, ES ;
SHAROV, VS ;
VLADIMIROV, YA .
FREE RADICAL BIOLOGY AND MEDICINE, 1993, 15 (03) :239-247
[7]  
FOLCH PIJ, 1957, J BIOL CHEM, V266, P499
[8]   ARE FREE-RADICALS INVOLVED IN LEAD-POISONING [J].
HERMESLIMA, M ;
PEREIRA, B ;
BECHARA, EJH .
XENOBIOTICA, 1991, 21 (08) :1085-1090
[10]   LIPID-PEROXIDATION IN WORKERS EXPOSED TO LEAD [J].
JIUN, YS ;
HSIEN, LT .
ARCHIVES OF ENVIRONMENTAL HEALTH, 1994, 49 (04) :256-259