Blanchflower W J, Walsh D M, Kennedy S, Kennedy D G
Department of Agriculture for Northern Ireland, Stormont, Belfast, United Kingdom.
Lipids. 1993 Mar;28(3):261-4. doi: 10.1007/BF02536650.
A method is presented for the determination of 4-hydroxynonenal (HNE) in tissue homogenates following in vitro lipid peroxidation induced by iron (Fe++). HNE is measured as the pentafluorobenzyl oxime derivative using liquid chromatography thermospray mass spectrometry. In vitro metabolism of HNE via the glutathione/glutathione-S-transferase pathway was inhibited using iodoacetic and iodobenzoic acids. The assay has been used as an indicator of the peroxidizability of tissue samples from animals both adequate in and depleted of alpha-tocopherol. The concentrations of HNE produced in tissues taken from animals depleted of alpha-tocopherol were found to be up to 8 times higher than those taken from animals supplemented with alpha-tocopherol.
本文介绍了一种测定铁(Fe++)诱导体外脂质过氧化后组织匀浆中4-羟基壬烯醛(HNE)的方法。采用液相色谱热喷雾质谱法将HNE作为五氟苄基肟衍生物进行测定。使用碘乙酸和碘苯甲酸抑制HNE通过谷胱甘肽/谷胱甘肽-S-转移酶途径的体外代谢。该测定法已被用作来自动物的组织样品过氧化能力的指标,这些动物的α-生育酚充足或缺乏。发现来自缺乏α-生育酚的动物的组织中产生的HNE浓度比来自补充α-生育酚的动物的组织中产生的HNE浓度高8倍。