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肠道黏膜脂质过氧化抑制剂的纯化及化学特性分析

Purification and chemical characterisation of the inhibitor of lipid peroxidation from intestinal mucosa.

作者信息

Diplock A T, Balasubramanian K A, Manohar M, Mathan V I, Ashton D

机构信息

Division of Biochemistry, United Medical School, London, U.K.

出版信息

Biochim Biophys Acta. 1988 Sep 2;962(1):42-50. doi: 10.1016/0005-2760(88)90093-8.

Abstract

The antioxidant previously isolated from intestinal mucosa has been subjected to further purification and identification. Although this inhibitor moved as a single spot on thin-layer chromatography in a number of different solvent systems, it proved to be a mixture of free carboxylic acids whose relative composition was similar in different batches. Detailed studies involving the use of high-pressure liquid chromatography, combined gas chromatography-mass spectrometry, high-field 360 MHz proton nuclear magnetic resonance spectroscopy, fast atom bombardment mass spectrometry and other techniques established that the inhibitor was a mixture of carboxylic acids of the following identity and relative composition (the major components comprising 92% of the total fatty acids): palmitic acid, 14.8%; palmitoleic acid, 3.6%; stearic acid, 7.0%; oleic acid, 21.0%; linoleic acid, 27.6% arachidonic acid, 18.0%. Mixtures of authentic fatty acids of the same relative concentration showed inhibition of peroxidation, comparable with the purified inhibitor from intestinal mucosa. A study of the inhibitory activity of the components of the mixture using malonaldehyde estimation, diene conjugation and arachidonic acid estimation showed that the inhibitory activity was due to palmitoleic and oleic acids only, the latter being the major component.

摘要

先前从肠黏膜中分离出的抗氧化剂已进行了进一步的纯化和鉴定。尽管这种抑制剂在多种不同的溶剂系统中,在薄层色谱上均呈现为单一斑点,但事实证明它是游离羧酸的混合物,其相对组成在不同批次中相似。涉及使用高压液相色谱、气相色谱 - 质谱联用、高场360兆赫质子核磁共振光谱、快原子轰击质谱等技术的详细研究表明,该抑制剂是具有以下特性和相对组成的羧酸混合物(主要成分占总脂肪酸的92%):棕榈酸,14.8%;棕榈油酸,3.6%;硬脂酸,7.0%;油酸,21.0%;亚油酸,27.6%;花生四烯酸,18.0%。具有相同相对浓度的真实脂肪酸混合物显示出与从肠黏膜纯化得到的抑制剂相当的过氧化抑制作用。使用丙二醛测定、二烯共轭和花生四烯酸测定对混合物成分的抑制活性进行的研究表明,抑制活性仅归因于棕榈油酸和油酸,其中油酸是主要成分。

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