Effect of aluminium on lipid peroxidation of human high density lipoproteins

被引:26
作者
Ferretti, G
Marchionni, C
Bacchetti, T
Galeazzi, T
Dousset, N
机构
[1] Univ Ancona, Inst Biochem, Fac Med, I-60131 Ancona, Italy
[2] Univ Toulouse 3, FR 1744, F-31062 Toulouse, France
关键词
aluminium; high density lipoproteins; iron; lipid peroxidation; physico-chemical properties; neurological diseases;
D O I
10.1080/1071576031000083125
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
We investigated the effect of aluminium (Al3+) on lipid peroxidation and physico-chemical properties of high density lipoproteins (HDL) isolated from human plasma. Our results demonstrated that Al3+ enhances lipid peroxidation of human HDL as shown by the significant increase in lipid hydroperoxides in Al-treated HDL with respect to control HDL. The oxidative effect was higher at acid pH (pH 5.5) with respect to pH 7.4. Moreover, a stimulating effect of Al3+ on iron-induced lipid peroxidation of HDL was demonstrated. The study of the effect of Al3+ on the physico-chemical properties of HDL, using the fluorescence polarization (Pf) of the probes TMA-DPH (1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene iodide) and DPH (1,6diphenyl-1,3,5-hexatriene), showed a significant decrease of Pf in Al-treated HDL with respect to control. These results suggest that Al3+ induces a decrease of molecular order at the lipoprotein surface. Moreover, the study of tryptophan (Trp) fluorescence demonstrated that aluminium induces structural modifications of HDL apoproteins and on HDL physico-chemical properties. The effect of Al3+ on lipid peroxidation of HDL was observed at aluminium concentrations similar to those observed in the brain of patients affected by neurological diseases. Aluminium-induced oxidative damage of HDL could be involved in the development of neurological diseases.
引用
收藏
页码:515 / 521
页数:7
相关论文
共 42 条
[1]   Modification of the lipid-protein interaction in human low-density lipoprotein destabilizes ApoB-100 and decreases oxidizability [J].
Abuja, PM ;
Lohner, K ;
Prassl, R .
BIOCHEMISTRY, 1999, 38 (11) :3401-3408
[2]   METABOLISM AND TOXICITY OF ALUMINUM IN RENAL-FAILURE [J].
ALFREY, AC ;
HEGG, A ;
CRASWELL, P .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1980, 33 (07) :1509-1516
[3]   Cerebrospinal fluid lipoproteins are more vulnerable to oxidation in Alzheimer's disease and are neurotoxic when oxidized ex vivo [J].
Bassett, CN ;
Neely, MD ;
Sidell, KR ;
Markesbery, WR ;
Swift, LL ;
Montine, TJ .
LIPIDS, 1999, 34 (12) :1273-1280
[4]  
Bassett CN, 2000, MICROSC RES TECHNIQ, V50, P282, DOI 10.1002/1097-0029(20000815)50:4<282::AID-JEMT6>3.0.CO
[5]  
2-T
[6]   CHARACTERIZATION OF THE CORE AND SURFACE OF HUMAN PLASMA-LIPOPROTEINS - A STUDY BASED ON THE USE OF 5 FLUOROPHORES [J].
BENYASHAR, V ;
BARENHOLZ, Y .
CHEMISTRY AND PHYSICS OF LIPIDS, 1991, 60 (01) :1-14
[7]  
BLASS JP, 1991, REV NEUROL, V147, P513
[8]   Estradiol enhances the resistance of LDL to oxidation by stabilizing apoB-100 conformation [J].
Brunelli, R ;
Mei, G ;
Krasnowska, EK ;
Pierucci, F ;
Zichella, L ;
Ursini, F ;
Parasassi, T .
BIOCHEMISTRY, 2000, 39 (45) :13897-13903
[9]   Oxidative stress and Alzheimer disease [J].
Christen, Y .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2000, 71 (02) :621S-629S
[10]  
CHUNG BH, 1986, METHOD ENZYMOL, V128, P181