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Abstract / Description of output
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 0.4-1.4μg/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 20μg/g, while that of cholesterol in mouse was 10-20mg/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.
Original language | English |
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Pages (from-to) | 229–234 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 449 |
Issue number | 2 |
Early online date | 14 May 2014 |
DOIs | |
Publication status | Published - 2014 |
Keywords / Materials (for Non-textual outputs)
- 24S,25-Epoxycholesterol
- 24S-hydroxycholesterol
- 3β,7α-Dihydroxycholest-5-en-24S,25-epoxide
- Brain
- Cytochrome P450 7b1
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