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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/).
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页码:768 / 774
页数:7
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