Abstract | AIMS: MAIN METHODS: Male C57Bl/6J mice were divided into four groups fed either a control diet alone (CT), or supplemented with simvastatin (0.1% w/w, Zocor®, MSD), or ezetimibe (0.021% w/w, Ezetrol®, MSD) or a combination of simvastatin and ezetimibe (0.1% and 0.021%, respectively) for one week. KEY FINDINGS: The combination of ezetimibe and simvastatin is required to observe a drop in cholesterolemia, linked to a huge activation of hepatic SREBP-2 and the consequent increased expression of genes involved in LDL cholesterol uptake and cholesterol synthesis. The gut microbiota analysis revealed no change in total bacteria, and in major Gram positive and Gram negative bacteria, but a selective significant increase in Lactobacillus spp. in mice treated with the ezetimibe and a decrease by the combination. The changes in lactobacilli level observed in ezetimibe or combination treated-mice are negatively correlated to expression of genes related to cholesterol metabolism. SIGNIFICANCE: The present study showed that ezetimibe taken alone is able to modify the composition of gut microbiota in favor of Lactobacillus spp. These results suggest that members of the genus Lactobacillus play an important role in cholesterol metabolism, even in normocholesterolemic mouse model.
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Authors | Emilie Catry, Barbara D Pachikian, Nuria Salazar, Audrey M Neyrinck, Patrice D Cani, Nathalie M Delzenne |
Journal | Life sciences
(Life Sci)
Vol. 132
Pg. 77-84
(Jul 01 2015)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 25916803
(Publication Type: Journal Article)
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Copyright | Copyright © 2015. Published by Elsevier Inc. |
Chemical References |
- Azetidines
- DNA Primers
- Srebf2 protein, mouse
- Sterol Regulatory Element Binding Protein 2
- Cholesterol
- Simvastatin
- Ezetimibe
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Topics |
- Analysis of Variance
- Animals
- Azetidines
(pharmacology)
- Blotting, Western
- Cholesterol
(biosynthesis, metabolism)
- DNA Primers
(genetics)
- Drug Evaluation, Preclinical
- Drug Therapy, Combination
- Ezetimibe
- Gastrointestinal Tract
(microbiology)
- Gene Expression Regulation
(drug effects, genetics)
- Lactobacillus
(drug effects, growth & development)
- Liver
(metabolism)
- Male
- Metabolic Networks and Pathways
(genetics)
- Mice
- Mice, Inbred C57BL
- Microbiota
(drug effects)
- Real-Time Polymerase Chain Reaction
- Simvastatin
(pharmacology)
- Sterol Regulatory Element Binding Protein 2
(metabolism)
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