Cargando…

Mechanism of Resistance to Dietary Cholesterol

Background. Alterations in expression of hepatic genes that could contribute to resistance to dietary cholesterol were investigated in Sprague-Dawley rats, which are known to be resistant to the serum cholesterol raising action of dietary cholesterol. Methods. Microarray analysis was used to provide...

Descripción completa

Detalles Bibliográficos
Autores principales: Boone, Lindsey R., Brooks, Patricia A., Niesen, Melissa I., Ness, Gene C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189572/
https://www.ncbi.nlm.nih.gov/pubmed/22007308
http://dx.doi.org/10.1155/2011/101242
_version_ 1782213481603268608
author Boone, Lindsey R.
Brooks, Patricia A.
Niesen, Melissa I.
Ness, Gene C.
author_facet Boone, Lindsey R.
Brooks, Patricia A.
Niesen, Melissa I.
Ness, Gene C.
author_sort Boone, Lindsey R.
collection PubMed
description Background. Alterations in expression of hepatic genes that could contribute to resistance to dietary cholesterol were investigated in Sprague-Dawley rats, which are known to be resistant to the serum cholesterol raising action of dietary cholesterol. Methods. Microarray analysis was used to provide a comprehensive analysis of changes in hepatic gene expression in rats in response to dietary cholesterol. Changes were confirmed by RT-PCR analysis. Western blotting was employed to measure changes in hepatic cholesterol 7α hydroxylase protein. Results. Of the 28,000 genes examined using the Affymetrix rat microarray, relatively few were significantly altered. As expected, decreases were observed for several genes that encode enzymes of the cholesterol biosynthetic pathway. The largest decreases were seen for squalene epoxidase and lanosterol 14α demethylase (CYP 51A1). These changes were confirmed by quantitative RT-PCR. LDL receptor expression was not altered by dietary cholesterol. Critically, the expression of cholesterol 7α hydroxylase, which catalyzes the rate-limiting step in bile acid synthesis, was increased over 4-fold in livers of rats fed diets containing 1% cholesterol. In contrast, mice, which are not resistant to dietary cholesterol, exhibited lower hepatic cholesterol 7α hydroxylase (CYP7A1) protein levels, which were not increased in response to diets containing 2% cholesterol.
format Online
Article
Text
id pubmed-3189572
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-31895722011-10-17 Mechanism of Resistance to Dietary Cholesterol Boone, Lindsey R. Brooks, Patricia A. Niesen, Melissa I. Ness, Gene C. J Lipids Research Article Background. Alterations in expression of hepatic genes that could contribute to resistance to dietary cholesterol were investigated in Sprague-Dawley rats, which are known to be resistant to the serum cholesterol raising action of dietary cholesterol. Methods. Microarray analysis was used to provide a comprehensive analysis of changes in hepatic gene expression in rats in response to dietary cholesterol. Changes were confirmed by RT-PCR analysis. Western blotting was employed to measure changes in hepatic cholesterol 7α hydroxylase protein. Results. Of the 28,000 genes examined using the Affymetrix rat microarray, relatively few were significantly altered. As expected, decreases were observed for several genes that encode enzymes of the cholesterol biosynthetic pathway. The largest decreases were seen for squalene epoxidase and lanosterol 14α demethylase (CYP 51A1). These changes were confirmed by quantitative RT-PCR. LDL receptor expression was not altered by dietary cholesterol. Critically, the expression of cholesterol 7α hydroxylase, which catalyzes the rate-limiting step in bile acid synthesis, was increased over 4-fold in livers of rats fed diets containing 1% cholesterol. In contrast, mice, which are not resistant to dietary cholesterol, exhibited lower hepatic cholesterol 7α hydroxylase (CYP7A1) protein levels, which were not increased in response to diets containing 2% cholesterol. Hindawi Publishing Corporation 2011 2011-10-05 /pmc/articles/PMC3189572/ /pubmed/22007308 http://dx.doi.org/10.1155/2011/101242 Text en Copyright © 2011 Lindsey R. Boone et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Boone, Lindsey R.
Brooks, Patricia A.
Niesen, Melissa I.
Ness, Gene C.
Mechanism of Resistance to Dietary Cholesterol
title Mechanism of Resistance to Dietary Cholesterol
title_full Mechanism of Resistance to Dietary Cholesterol
title_fullStr Mechanism of Resistance to Dietary Cholesterol
title_full_unstemmed Mechanism of Resistance to Dietary Cholesterol
title_short Mechanism of Resistance to Dietary Cholesterol
title_sort mechanism of resistance to dietary cholesterol
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189572/
https://www.ncbi.nlm.nih.gov/pubmed/22007308
http://dx.doi.org/10.1155/2011/101242
work_keys_str_mv AT boonelindseyr mechanismofresistancetodietarycholesterol
AT brookspatriciaa mechanismofresistancetodietarycholesterol
AT niesenmelissai mechanismofresistancetodietarycholesterol
AT nessgenec mechanismofresistancetodietarycholesterol