Oxysterols in the brain of the cholesterol 24-hydroxylase knockout mouse

被引:39
作者
Meljon, Anna [1 ]
Wang, Yuqin [1 ]
Griffiths, William J. [1 ]
机构
[1] Swansea Univ, Coll Med, Inst Mass Spectrometry, Swansea SA2 8PP, W Glam, Wales
基金
英国生物技术与生命科学研究理事会;
关键词
24S-Hydroxycholesterol; 24R-Hydroxycholesterol; 24S; 25-Epoxycholesterol; Oxysterol; Brain; Cyp46a1; LIVER X RECEPTORS; MASS-SPECTROMETRY; ALZHEIMERS-DISEASE; METABOLISM; TURNOVER; CELLS; BILE; 24S-HYDROXYCHOLESTEROL; 25-HYDROXYCHOLESTEROL; HOMEOSTASIS;
D O I
10.1016/j.bbrc.2014.01.153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxysterols are oxidised forms of cholesterol or its precursors. In this study we utilised the cholesterol 24-hydroxylase knockout mouse (Cyp46a1-/-) to study the sterol and oxysterol content of brain. Despite a great reduction in the abundance of 24S-hydroxycholesterol, the dominant metabolite of cholesterol in wild type brain, no other cholesterol metabolite was found to quantitatively replace this oxysterol in the Cyp46a1-/- mouse. Only minor amounts of other side-chain oxysterols including 22R-, 24R-, 25- and (25R),26-hydroxycholesterols were detected. In line with earlier studies, levels of cholesterol were similar in Cyp46a1-/- and wild type animals. However, the level of the cholesterol precursor, desomsterol, and its parallel metabolite formed via a shut of the mevalonate pathway, 24S,25-epoxycholesterol, were reduced in the Cyp46a1-/- mouse. The reduction in abundance of 24S,25-epoxycholesterol is interesting in light of a recent report indicating that this oxysterol promotes dopaminergic neurogenesis. (C) 2014 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
引用
收藏
页码:768 / 774
页数:7
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