INHIBITION OF CA2+-INDUCED AGGREGATION OF PORCINE INTESTINAL BRUSH-BORDER MEMBRANES BY LIPID-PEROXIDATION

被引:0
|
作者
OHYASHIKI, T
TAKINO, T
MATSUI, K
机构
[1] Department of Biochemistry, Faculty of Pharmaceutical Sciences, Hokuriku University, Kanazawa, Ishikawa 920-11, Kanagawa-machi
来源
JOURNAL OF BIOCHEMISTRY | 1994年 / 116卷 / 02期
关键词
INTESTINAL BRUSH-BORDER MEMBRANE; MEMBRANE AGGREGATION; MEMBRANE INTERACTION; OXIDATIVE DAMAGE;
D O I
10.1093/oxfordjournals.jbchem.a124531
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 effects of lipid peroxidation on Ca2+-induced aggregation of porcine intestinal brush-border membranes were examined using a system consisting of ascorbic acid/Fe2+/tert-butyl hydroperoxide (t-BuOOH). Incubation of the membranes with ascorbic acid/Fe2+/t-BuOOH resulted in inhibition of Ca2+-induced aggregation of the membranes with the formation of thiobarbituric acid-reactive substances, depending on the hydroperoxide concentration and the incubation time. The inhibition of the membrane aggregation associated with ascorbic acid/Fe2+/t-BuOOH treatment was effectively prevented by the addition of an antioxidant, 3(2)-tert-butyl-4-hydroxyanisole, to the reaction mixture. Studies with 8-anilino-1-naphthalenesulfonate (ANS) revealed that there is a linear relationship between the apparent dissociation constants (K-d) of ANS-membrane complexes and the aggregating efficiencies of the membranes with different levels of lipid peroxidation. This suggests that inhibition of the membrane aggregation by lipid peroxidation involves a change in the membrane surface charge density. Modification of the membranes with malondialdehyde also resulted in a decrease in the aggregating efficiency of the membranes with a decrease in the K-d value of ANS-membrane complex. In addition, the contribution of the lipid organization to membrane aggregation was examined by measuring the fluorescence anisotropy of diphenylhexatriene-labeled membranes in the presence of a lipid fluidizer, benzyl alcohol. The results are discussed in terms of peroxidation-induced inhibition of intramembrane interactions of the membranes.
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页码:351 / 356
页数:6
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