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24S,25-Epoxycholesterol in mouse and rat brain
24S,25-Epoxycholesterol is formed in a shunt of the mevalonate pathway that produces cholesterol. It is one of the most potent known activators of the liver X receptors and can inhibit sterol regulatory element-binding protein processing. Until recently analysis of 24S,25-epoxycholesterol at high se...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053837/ https://www.ncbi.nlm.nih.gov/pubmed/24832732 http://dx.doi.org/10.1016/j.bbrc.2014.05.012 |
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author | Wang, Yuchen Karu, Kersti Meljon, Anna Turton, John Yau, Joyce L. Seckl, Jonathan R. Wang, Yuqin Griffiths, William J. |
author_facet | Wang, Yuchen Karu, Kersti Meljon, Anna Turton, John Yau, Joyce L. Seckl, Jonathan R. Wang, Yuqin Griffiths, William J. |
author_sort | Wang, Yuchen |
collection | PubMed |
description | 24S,25-Epoxycholesterol is formed in a shunt of the mevalonate pathway that produces cholesterol. It is one of the most potent known activators of the liver X receptors and can inhibit sterol regulatory element-binding protein processing. Until recently analysis of 24S,25-epoxycholesterol at high sensitivity has been precluded by its thermal lability and lack of a strong chromophore. Here we report on the analysis of 24S,25-epoxycholesterol in rodent brain where its level was determined to be of the order of 0.4–1.4 μg/g wet weight in both adult mouse and rat. For comparison the level of 24S-hydroxycholesterol in brain of both rodents was of the order of 20 μg/g, while that of cholesterol in mouse was 10–20 mg/g. By exploiting knockout mice for the enzyme oxysterol 7α-hydroxylase (Cyp7b1) we show that this enzymes is important for the subsequent metabolism of the 24S,25-epoxide. |
format | Online Article Text |
id | pubmed-4053837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40538372014-06-27 24S,25-Epoxycholesterol in mouse and rat brain Wang, Yuchen Karu, Kersti Meljon, Anna Turton, John Yau, Joyce L. Seckl, Jonathan R. Wang, Yuqin Griffiths, William J. Biochem Biophys Res Commun Article 24S,25-Epoxycholesterol is formed in a shunt of the mevalonate pathway that produces cholesterol. It is one of the most potent known activators of the liver X receptors and can inhibit sterol regulatory element-binding protein processing. Until recently analysis of 24S,25-epoxycholesterol at high sensitivity has been precluded by its thermal lability and lack of a strong chromophore. Here we report on the analysis of 24S,25-epoxycholesterol in rodent brain where its level was determined to be of the order of 0.4–1.4 μg/g wet weight in both adult mouse and rat. For comparison the level of 24S-hydroxycholesterol in brain of both rodents was of the order of 20 μg/g, while that of cholesterol in mouse was 10–20 mg/g. By exploiting knockout mice for the enzyme oxysterol 7α-hydroxylase (Cyp7b1) we show that this enzymes is important for the subsequent metabolism of the 24S,25-epoxide. Academic Press 2014-06-27 /pmc/articles/PMC4053837/ /pubmed/24832732 http://dx.doi.org/10.1016/j.bbrc.2014.05.012 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Wang, Yuchen Karu, Kersti Meljon, Anna Turton, John Yau, Joyce L. Seckl, Jonathan R. Wang, Yuqin Griffiths, William J. 24S,25-Epoxycholesterol in mouse and rat brain |
title | 24S,25-Epoxycholesterol in mouse and rat brain |
title_full | 24S,25-Epoxycholesterol in mouse and rat brain |
title_fullStr | 24S,25-Epoxycholesterol in mouse and rat brain |
title_full_unstemmed | 24S,25-Epoxycholesterol in mouse and rat brain |
title_short | 24S,25-Epoxycholesterol in mouse and rat brain |
title_sort | 24s,25-epoxycholesterol in mouse and rat brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053837/ https://www.ncbi.nlm.nih.gov/pubmed/24832732 http://dx.doi.org/10.1016/j.bbrc.2014.05.012 |
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