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Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans

Visceral obesity and fatty liver have been related to high synthesis and low absorption of cholesterol. This study aimed to investigate the associations of cholesterol metabolism with liver and visceral fat content in healthy humans. Another objective was to explore the effects of very-high-fructose...

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Autores principales: Silbernagel, Guenther, Lütjohann, Dieter, Machann, Juergen, Meichsner, Sabrina, Kantartzis, Konstantinos, Schick, Fritz, Häring, Hans-Ulrich, Stefan, Norbert, Fritsche, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235776/
https://www.ncbi.nlm.nih.gov/pubmed/22203835
http://dx.doi.org/10.1155/2012/361863
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author Silbernagel, Guenther
Lütjohann, Dieter
Machann, Juergen
Meichsner, Sabrina
Kantartzis, Konstantinos
Schick, Fritz
Häring, Hans-Ulrich
Stefan, Norbert
Fritsche, Andreas
author_facet Silbernagel, Guenther
Lütjohann, Dieter
Machann, Juergen
Meichsner, Sabrina
Kantartzis, Konstantinos
Schick, Fritz
Häring, Hans-Ulrich
Stefan, Norbert
Fritsche, Andreas
author_sort Silbernagel, Guenther
collection PubMed
description Visceral obesity and fatty liver have been related to high synthesis and low absorption of cholesterol. This study aimed to investigate the associations of cholesterol metabolism with liver and visceral fat content in healthy humans. Another objective was to explore the effects of very-high-fructose and very-high-glucose diets on cholesterol homeostasis. We report on a cohort of 20 people (12 males, 8 females; age 30.5 ± 2.0 years; body mass index 25.9 ± 0.5 kg/m(2)) who completed a four-week dietary intervention study. Between the baseline and the followup examination the study participants in addition to a balanced weight-maintaining diet received 150 g of either fructose or glucose per day. Visceral and liver fat were measured with magnetic resonance (MR) imaging and (1)H-MR spectroscopy, respectively. Cholesterol absorption and synthesis were estimated from the serum noncholesterol sterol concentrations. Performing cross-sectional analyses the lanosterol and desmosterol to cholesterol ratios were positively correlated with visceral and liver fat content (all P < .03). The lathosterol to cholesterol ratio decreased in response to high-fructose diet (P = .006) but not in response to high-glucose diet. To conclude, visceral and liver fat content are associated with cholesterol synthesis in healthy humans. Furthermore, cholesterol synthesis appears to be dependent on fructose/glucose intake.
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spelling pubmed-32357762011-12-27 Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans Silbernagel, Guenther Lütjohann, Dieter Machann, Juergen Meichsner, Sabrina Kantartzis, Konstantinos Schick, Fritz Häring, Hans-Ulrich Stefan, Norbert Fritsche, Andreas Exp Diabetes Res Research Article Visceral obesity and fatty liver have been related to high synthesis and low absorption of cholesterol. This study aimed to investigate the associations of cholesterol metabolism with liver and visceral fat content in healthy humans. Another objective was to explore the effects of very-high-fructose and very-high-glucose diets on cholesterol homeostasis. We report on a cohort of 20 people (12 males, 8 females; age 30.5 ± 2.0 years; body mass index 25.9 ± 0.5 kg/m(2)) who completed a four-week dietary intervention study. Between the baseline and the followup examination the study participants in addition to a balanced weight-maintaining diet received 150 g of either fructose or glucose per day. Visceral and liver fat were measured with magnetic resonance (MR) imaging and (1)H-MR spectroscopy, respectively. Cholesterol absorption and synthesis were estimated from the serum noncholesterol sterol concentrations. Performing cross-sectional analyses the lanosterol and desmosterol to cholesterol ratios were positively correlated with visceral and liver fat content (all P < .03). The lathosterol to cholesterol ratio decreased in response to high-fructose diet (P = .006) but not in response to high-glucose diet. To conclude, visceral and liver fat content are associated with cholesterol synthesis in healthy humans. Furthermore, cholesterol synthesis appears to be dependent on fructose/glucose intake. Hindawi Publishing Corporation 2012 2011-11-29 /pmc/articles/PMC3235776/ /pubmed/22203835 http://dx.doi.org/10.1155/2012/361863 Text en Copyright © 2012 Guenther Silbernagel 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
Silbernagel, Guenther
Lütjohann, Dieter
Machann, Juergen
Meichsner, Sabrina
Kantartzis, Konstantinos
Schick, Fritz
Häring, Hans-Ulrich
Stefan, Norbert
Fritsche, Andreas
Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title_full Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title_fullStr Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title_full_unstemmed Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title_short Cholesterol Synthesis Is Associated with Hepatic Lipid Content and Dependent on Fructose/Glucose Intake in Healthy Humans
title_sort cholesterol synthesis is associated with hepatic lipid content and dependent on fructose/glucose intake in healthy humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235776/
https://www.ncbi.nlm.nih.gov/pubmed/22203835
http://dx.doi.org/10.1155/2012/361863
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