Suppr超能文献

胆汁酸对脂质过氧化的影响:铁的作用。

Effect of bile acids on lipid peroxidation: the role of iron.

作者信息

Sreejayan N, von Ritter C

机构信息

Department of Medicine II, Klinikum Grosshadern, Ludwig-Maximilians-University, Munich, Germany.

出版信息

Free Radic Biol Med. 1998 Jul 1;25(1):50-6. doi: 10.1016/s0891-5849(98)00045-8.

Abstract

The toxic effect of hydrophobic bile acids is claimed to be in part mediated by lipid peroxidation. Conversely, antioxidant properties of tauroursodeoxycholic acid (TUDC), a hydrophilic bile acid, have been suggested as a possible mechanism by which TUDC confers its beneficial effect in a variety of diseases. We have investigated the effect of taurodeoxycholic acid (TDC), a hydrophobic bile acid and TUDC on lipid peroxidation using a pure lipid system both in the presence and absence of iron ions. Neither TDC nor TUDC showed any effect on spontaneous lipid peroxidation of phosphatidylcholine liposomes or sodium arachidonate solution. This lack of effect excludes the possibility of direct prooxidant or antioxidant properties for TDC and TUDC. Addition of ferrous ions (0.1 mM) to the lipid system brought about a linear increase in lipid peroxidation with time. The presence of TDC caused an increase in the rate and extent of iron-stimulated lipid peroxidation. The propensity of bile acids to increase iron-induced lipid peroxidation was related to hydrophobicity of the individual bile acids, with the highest effect observed with taurolithocholic acid, whereas TUDC did not have any influence. The TDC-induced increase in the iron-stimulated lipid peroxidation was concentration dependent. Addition of TUDC (10 mM) completely abolished the effect of TDC (2 mM) on iron-induced lipid peroxidation. This finding suggests that TUDC does not function as an antioxidant per se but may prevent lipid peroxidation caused by TDC. In conclusion, only in the presence of iron ions, hydrophobic bile acids may enhance lipid peroxidation. TUDC has no antioxidant activity per se but may counter the TDC-induced increase in iron-stimulated lipid peroxidation.

摘要

疏水胆汁酸的毒性作用据称部分是由脂质过氧化介导的。相反,牛磺熊去氧胆酸(TUDC)作为一种亲水胆汁酸,其抗氧化特性被认为是TUDC在多种疾病中发挥有益作用的一种可能机制。我们使用纯脂质系统,在有和没有铁离子的情况下,研究了疏水胆汁酸牛磺脱氧胆酸(TDC)和TUDC对脂质过氧化的影响。TDC和TUDC对磷脂酰胆碱脂质体或花生四烯酸钠溶液的自发脂质过氧化均无任何影响。这种无影响排除了TDC和TUDC具有直接促氧化或抗氧化特性的可能性。向脂质系统中加入亚铁离子(0.1 mM)会导致脂质过氧化随时间呈线性增加。TDC的存在导致铁刺激的脂质过氧化速率和程度增加。胆汁酸增加铁诱导的脂质过氧化的倾向与各个胆汁酸的疏水性有关,牛磺石胆酸的作用最为明显,而TUDC没有任何影响。TDC诱导的铁刺激的脂质过氧化增加具有浓度依赖性。加入TUDC(10 mM)完全消除了TDC(2 mM)对铁诱导的脂质过氧化的影响。这一发现表明,TUDC本身并不作为抗氧化剂起作用,但可能预防由TDC引起的脂质过氧化。总之,只有在存在铁离子的情况下,疏水胆汁酸才可能增强脂质过氧化。TUDC本身没有抗氧化活性,但可能抵消TDC诱导的铁刺激的脂质过氧化增加。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验