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脂质过氧化对钙离子诱导的猪小肠刷状缘膜聚集的抑制作用。

Inhibition of Ca(2+)-induced aggregation of porcine intestinal brush-border membranes by lipid peroxidation.

作者信息

Ohyashiki T, Takino T, Matsui K

机构信息

Department of Biochemistry, Faculty of Pharmaceutical Sciences, Hokuriku University, Ishikawa.

出版信息

J Biochem. 1994 Aug;116(2):351-6. doi: 10.1093/oxfordjournals.jbchem.a124531.

Abstract

The effects of lipid peroxidation on Ca(2+)-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 Ca(2+)-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 (Kd) 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 Kd 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.

摘要

使用由抗坏血酸/Fe²⁺/叔丁基过氧化氢(t-BuOOH)组成的系统,研究了脂质过氧化对猪小肠刷状缘膜Ca²⁺诱导聚集的影响。将膜与抗坏血酸/Fe²⁺/t-BuOOH一起孵育,会导致膜的Ca²⁺诱导聚集受到抑制,并形成硫代巴比妥酸反应性物质,这取决于氢过氧化物浓度和孵育时间。通过向反应混合物中添加抗氧化剂3(2)-叔丁基-4-羟基茴香醚,可有效防止与抗坏血酸/Fe²⁺/t-BuOOH处理相关的膜聚集抑制。用8-苯胺基-1-萘磺酸盐(ANS)进行的研究表明,ANS-膜复合物的表观解离常数(Kd)与具有不同脂质过氧化水平的膜的聚集效率之间存在线性关系。这表明脂质过氧化对膜聚集的抑制涉及膜表面电荷密度的变化。用丙二醛对膜进行修饰也导致膜的聚集效率降低,同时ANS-膜复合物的Kd值降低。此外,通过在脂质流化剂苄醇存在下测量二苯基己三烯标记膜的荧光各向异性,研究了脂质组织对膜聚集的贡献。根据过氧化诱导的膜内相互作用抑制来讨论结果。

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