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首页> 外文期刊>Chemical research in toxicology >Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation.
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Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation.

机译:表征4-氧代-2-壬烯醛作为脂质过氧化的新产物。

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Fe(II)-mediated decomposition of 13-[S-(Z,E)]-9, 11-hydroperoxyoctadecadienoic (hydroperoxylinoleic) acid resulted in the formation of three alpha,beta-unsaturated aldehydes. At low Fe(II) concentrations or at early time points after the addition of Fe(II), two major products were observed. The least polar product had chromatographic properties that were identical with those of 4-oxo-2-nonenal. Conversion of this product to its bis-oxime derivative with hydroxylamine hydrochloride resulted in two syn- and two anti-oxime isomers that had chromatographic and mass spectral properties identical with the properties of products derived from an authentic standard of 4-oxo-2-nonenal. This confirmed for the first time that 4-oxo-2-nonenal is a major product of the Fe(II)-mediated breakdown of lipid hydroperoxides. The more polar product had chromatographic properties that were similar to those of 4-hydroperoxy-2-nonenal. LC/MS analysis of its syn- and anti-oxime isomers confirmed this structural assignment. Thus, 4-hydroperoxy-2-nonenal is a previously unrecognized major product of lipid hydroperoxide decomposition. At high Fe(II) concentrations and at longer incubation times, a third more polar product was observed with chromatographic properties that were identical to those of 4-hydroxy-2-nonenal. The syn- and anti-oxime isomers had chromatographic and mass spectral properties identical with the properties of products derived from an authentic standard of 4-hydroxy-2-nonenal. It appears that 4-hydroperoxy-2-nonenal is formed initially and that it is then converted to 4-hydroxy-2-nonenal in the presence of high Fe(II) concentrations or by extended incubations in the presence of low Fe(II) concentrations. It is conceivable that some of the 4-hydroperoxy-2-nonenal is also converted to 4-oxo-2-nonenal. However, we cannot rule out the possibility that it is also formed by a concerted mechanism from a rearrangement product of 13-[S-(Z,E)]-9, 11-hydroperoxyoctadecadienoic acid.
机译:Fe(II)介导的13- [S-(Z,E)]-9,11-氢过氧十八碳二烯酸(氢过氧亚油酸)的分解导致形成三个α,β-不饱和醛。在低Fe(II)浓度或添加Fe(II)之后的早期时间点,观察到两种主要产物。极性最小的产物具有与4-氧-2-壬烯醛相同的色谱性质。用盐酸羟胺将该产物转化为其双肟衍生物,得到两种顺式和两种抗肟异构体,其异构体的色谱和质谱性质与真实的4-氧代-2-壬烯醛标准品的性质相同。 。这首次证实4-氧代-2-壬烯醛是Fe(II)介导的脂质氢过氧化物分解的主要产物。极性更大的产物具有与4-氢过氧-2-壬烯类似的色谱性质。 LC / MS分析其合成和抗肟异构体证实了这种结构。因此,4-氢过氧-2-壬烯醛是脂质氢过氧化物分解的先前未被认识的主要产物。在高Fe(II)浓度和更长的孵育时间下,观察到第三种极性更大的产物,其色谱性质与4-羟基-2-壬烯醛相同。顺式和反式肟异构体的色谱和质谱性质与衍生自真实标准4-羟基-2-壬烯醛的产品的性质相同。似乎最初形成了4-hydroperoxy-2-nonenal,然后在高Fe(II)浓度下或在低Fe(II)的条件下进行了长时间孵育,将其转化为4-羟基-2-壬烯醛。浓度。可以想象一些4-氢过氧-2-壬烯醛也被转化为4-氧代-2-壬烯醛。但是,我们不能排除它也可能是由13- [S-(Z,E)]-9,11-氢过氧十八碳二烯酸的重排产物通过协同机制形成的。

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