The oxysterols 7 beta-hydroxycholesterol and 7-ketocholesterol are cholesterol autoxidation products. These two oxysterols are formed as a result of low density lipoprotein oxidation and in a study on biomarkers for oxidative stress in patients with atherosclerosis, 7 beta-hydroxycholesterol was found to be the strongest predictor of progression of carotid atherosclerosis. Interconversion of 7 beta-hydroxycholesterol and 7-ketocholesterol in vitro has been reported recently, using recombinant 11 beta-hydroxysteroid dehydrogenase or rodent liver microsomes. In this study deuterium-labeled 7 beta-hydroxycholesterol or 7-ketocholesterol was administered intravenously to two healthy volunteers and blood samples were collected at different time points. The mean half-life for elimination of 7 beta-hydroxycholesterol from the circulation was estimated to be 1.9 h. The corresponding half-life for 7-ketocholesterol was estimated to be 1.5 h. Infusion of deuterium-labeled 7-ketocholesterol resulted in labeling of 7 beta-hydroxycholesterol and vice versa. In addition, the biological within-day and between-day variations of the two oxysterols were determined. In summary, the present investigation clearly shows an interconversion of 7 beta-hydroxycholesterol and 7-ketocholesterol in humans.

In vivo interconversion of 7beta-hydroxycholesterol and 7-ketocholesterol, potential surrogate markers for oxidative stress / Larsson, H; Böttiger, Y; Iuliano, Luigi; Diczfalusy, U.. - In: FREE RADICAL BIOLOGY & MEDICINE. - ISSN 0891-5849. - STAMPA. - 43:(2007), pp. 695-701. [10.1016/j.freeradbiomed.2007.04.033]

In vivo interconversion of 7beta-hydroxycholesterol and 7-ketocholesterol, potential surrogate markers for oxidative stress

IULIANO, Luigi;
2007

Abstract

The oxysterols 7 beta-hydroxycholesterol and 7-ketocholesterol are cholesterol autoxidation products. These two oxysterols are formed as a result of low density lipoprotein oxidation and in a study on biomarkers for oxidative stress in patients with atherosclerosis, 7 beta-hydroxycholesterol was found to be the strongest predictor of progression of carotid atherosclerosis. Interconversion of 7 beta-hydroxycholesterol and 7-ketocholesterol in vitro has been reported recently, using recombinant 11 beta-hydroxysteroid dehydrogenase or rodent liver microsomes. In this study deuterium-labeled 7 beta-hydroxycholesterol or 7-ketocholesterol was administered intravenously to two healthy volunteers and blood samples were collected at different time points. The mean half-life for elimination of 7 beta-hydroxycholesterol from the circulation was estimated to be 1.9 h. The corresponding half-life for 7-ketocholesterol was estimated to be 1.5 h. Infusion of deuterium-labeled 7-ketocholesterol resulted in labeling of 7 beta-hydroxycholesterol and vice versa. In addition, the biological within-day and between-day variations of the two oxysterols were determined. In summary, the present investigation clearly shows an interconversion of 7 beta-hydroxycholesterol and 7-ketocholesterol in humans.
2007
LOW-DENSITY-LIPOPROTEIN; RAPID HEPATIC-METABOLISM; STEROL 27-HYDROXYLASE; 11-BETA-HYDROXYSTEROID DEHYDROGENASE; DIABETES-MELLITUS; VITAMIN-E; 7-ALPHA-HYDROXYCHOLESTEROL DEHYDROGENASE; MASS-SPECTROMETRY; PLASMA-LEVELS; CHOLESTEROL
01 Pubblicazione su rivista::01a Articolo in rivista
In vivo interconversion of 7beta-hydroxycholesterol and 7-ketocholesterol, potential surrogate markers for oxidative stress / Larsson, H; Böttiger, Y; Iuliano, Luigi; Diczfalusy, U.. - In: FREE RADICAL BIOLOGY & MEDICINE. - ISSN 0891-5849. - STAMPA. - 43:(2007), pp. 695-701. [10.1016/j.freeradbiomed.2007.04.033]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/109048
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