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人中性粒细胞微粒体形成脂氧素A4的一种新型20-羟基化代谢物。

Formation of a novel 20-hydroxylated metabolite of lipoxin A4 by human neutrophil microsomes.

作者信息

Sumimoto H, Isobe R, Mizukami Y, Minakami S

机构信息

Department of Biochemistry, Kyushu University School of Medicine, Fukuoka, Japan.

出版信息

FEBS Lett. 1993 Jan 11;315(3):205-10. doi: 10.1016/0014-5793(93)81165-v.

Abstract

Lipoxin A4 (LXA4) is a biologically active compound produced from arachidonic acid via interactions of lipoxygenases. Incubation of LXA4 either with human neutrophils or with the neutrophil microsomes leads to formation of a polar compound on a reverse-phase high-performance liquid chromatography. We have identified the metabolite as 20-hydroxy-LXA4, a novel metabolite of arachidonic acid, on the basis of ultraviolet spectrometry and gas chromatography-mass spectrometry. The LXA4 omega-hydroxylation requires both molecular oxygen and NADPH, and is inhibited by carbon monoxide, by antibodies raised against NADPH-cytochrome P-450 reductase, or competitively by leukotriene B4 (LTB4) and LTB5, substrates of LTB4 omega-hydroxylase. These findings indicate that the formation of 20-hydroxy-LXA4 is catalyzed by a neutrophil cytochrome P-450, the LTB4 omega-hydroxylase.

摘要

脂氧素A4(LXA4)是一种通过脂氧合酶相互作用由花生四烯酸产生的生物活性化合物。将LXA4与人中性粒细胞或中性粒细胞微粒体一起孵育会导致在反相高效液相色谱上形成一种极性化合物。基于紫外光谱法和气相色谱 - 质谱法,我们已将该代谢物鉴定为20 - 羟基 - LXA4,一种花生四烯酸的新型代谢物。LXA4的ω - 羟基化需要分子氧和NADPH,并且受到一氧化碳、针对NADPH - 细胞色素P - 450还原酶产生的抗体的抑制,或者被白三烯B4(LTB4)和LTB5竞争性抑制,LTB4和LTB5是LTB4 ω - 羟化酶的底物基团。这些发现表明20 - 羟基 - LXA4的形成是由中性粒细胞细胞色素P - 450(即LTB4 ω - 羟化酶)催化的。

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