Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice
Statins are competitive inhibitors of HMG-CoA reductase, the rate-limiting enzyme of cholesterol synthesis. Statins reduce plasma cholesterol levels, but whether this is actually caused by inhibition of de novo cholesterol synthesis has not been clearly established. Using three different statins, we...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2016-08-01
|
Series: | Journal of Lipid Research |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520352172 |
id |
doaj-b3500345d1e24fb89a415e9be656e6dd |
---|---|
record_format |
Article |
spelling |
doaj-b3500345d1e24fb89a415e9be656e6dd2021-04-29T04:38:08ZengElsevierJournal of Lipid Research0022-22752016-08-0157814551464Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in miceMarleen Schonewille0Jan Freark de Boer1Laura Mele2Henk Wolters3Vincent W. Bloks4Justina C. Wolters5Jan A. Kuivenhoven6Uwe J.F. Tietge7Gemma Brufau8Albert K. Groen9To whom correspondence should be addressed; Department of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The Netherlands; To whom correspondence should be addressedDepartment of Pediatrics, Section Molecular Genetics,University Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of Pediatrics, Section Molecular Genetics,University Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of Pediatrics, Section Molecular Genetics,University Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The NetherlandsDepartment of PediatricsUniversity Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Department of Laboratory Medicine, Center for Liver, Digestive and Metabolic Diseases, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Amsterdam Diabetes Center, Department of Vascular Medicine,Academic Medical Center, The NetherlandsStatins are competitive inhibitors of HMG-CoA reductase, the rate-limiting enzyme of cholesterol synthesis. Statins reduce plasma cholesterol levels, but whether this is actually caused by inhibition of de novo cholesterol synthesis has not been clearly established. Using three different statins, we investigated the effects on cholesterol metabolism in mice in detail. Surprisingly, direct measurement of whole body cholesterol synthesis revealed that cholesterol synthesis was robustly increased in statin-treated mice. Measurement of organ-specific cholesterol synthesis demonstrated that the liver is predominantly responsible for the increase in cholesterol synthesis. Excess synthesized cholesterol did not accumulate in the plasma, as plasma cholesterol decreased. However, statin treatment led to an increase in cholesterol removal via the feces. Interestingly, enhanced cholesterol excretion in response to rosuvastatin and lovastatin treatment was mainly mediated via biliary cholesterol secretion, whereas atorvastatin mainly stimulated cholesterol removal via the transintestinal cholesterol excretion pathway. Moreover, we show that plasma cholesterol precursor levels do not reflect cholesterol synthesis rates during statin treatment in mice. In conclusion, cholesterol synthesis is paradoxically increased upon statin treatment in mice. However, statins potently stimulate the excretion of cholesterol from the body, which sheds new light on possible mechanisms underlying the cholesterol-lowering effects of statins.http://www.sciencedirect.com/science/article/pii/S0022227520352172cholesterol/absorptioncholesterol/biosynthesisliverintestinebiliary cholesteroltransintestinal cholesterol excretion |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marleen Schonewille Jan Freark de Boer Laura Mele Henk Wolters Vincent W. Bloks Justina C. Wolters Jan A. Kuivenhoven Uwe J.F. Tietge Gemma Brufau Albert K. Groen |
spellingShingle |
Marleen Schonewille Jan Freark de Boer Laura Mele Henk Wolters Vincent W. Bloks Justina C. Wolters Jan A. Kuivenhoven Uwe J.F. Tietge Gemma Brufau Albert K. Groen Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice Journal of Lipid Research cholesterol/absorption cholesterol/biosynthesis liver intestine biliary cholesterol transintestinal cholesterol excretion |
author_facet |
Marleen Schonewille Jan Freark de Boer Laura Mele Henk Wolters Vincent W. Bloks Justina C. Wolters Jan A. Kuivenhoven Uwe J.F. Tietge Gemma Brufau Albert K. Groen |
author_sort |
Marleen Schonewille |
title |
Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
title_short |
Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
title_full |
Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
title_fullStr |
Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
title_full_unstemmed |
Statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
title_sort |
statins increase hepatic cholesterol synthesis and stimulate fecal cholesterol elimination in mice |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
2016-08-01 |
description |
Statins are competitive inhibitors of HMG-CoA reductase, the rate-limiting enzyme of cholesterol synthesis. Statins reduce plasma cholesterol levels, but whether this is actually caused by inhibition of de novo cholesterol synthesis has not been clearly established. Using three different statins, we investigated the effects on cholesterol metabolism in mice in detail. Surprisingly, direct measurement of whole body cholesterol synthesis revealed that cholesterol synthesis was robustly increased in statin-treated mice. Measurement of organ-specific cholesterol synthesis demonstrated that the liver is predominantly responsible for the increase in cholesterol synthesis. Excess synthesized cholesterol did not accumulate in the plasma, as plasma cholesterol decreased. However, statin treatment led to an increase in cholesterol removal via the feces. Interestingly, enhanced cholesterol excretion in response to rosuvastatin and lovastatin treatment was mainly mediated via biliary cholesterol secretion, whereas atorvastatin mainly stimulated cholesterol removal via the transintestinal cholesterol excretion pathway. Moreover, we show that plasma cholesterol precursor levels do not reflect cholesterol synthesis rates during statin treatment in mice. In conclusion, cholesterol synthesis is paradoxically increased upon statin treatment in mice. However, statins potently stimulate the excretion of cholesterol from the body, which sheds new light on possible mechanisms underlying the cholesterol-lowering effects of statins. |
topic |
cholesterol/absorption cholesterol/biosynthesis liver intestine biliary cholesterol transintestinal cholesterol excretion |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520352172 |
work_keys_str_mv |
AT marleenschonewille statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT janfrearkdeboer statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT lauramele statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT henkwolters statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT vincentwbloks statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT justinacwolters statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT janakuivenhoven statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT uwejftietge statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT gemmabrufau statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice AT albertkgroen statinsincreasehepaticcholesterolsynthesisandstimulatefecalcholesteroleliminationinmice |
_version_ |
1721502262513106944 |