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Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice

OBJECTIVE—: To investigate the effect of gut microbiota and diet on atherogenesis. APPROACH AND RESULTS—: Here, we investigated the interaction between the gut microbiota and diet on atherosclerosis by feeding germ-free or conventionally raised Apoe(−/−) mice chow or Western diet alone or supplement...

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Autores principales: Lindskog Jonsson, Annika, Caesar, Robert, Akrami, Rozita, Reinhardt, Christoph, Fåk Hållenius, Frida, Borén, Jan, Bäckhed, Fredrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166703/
https://www.ncbi.nlm.nih.gov/pubmed/29903735
http://dx.doi.org/10.1161/ATVBAHA.118.311233
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author Lindskog Jonsson, Annika
Caesar, Robert
Akrami, Rozita
Reinhardt, Christoph
Fåk Hållenius, Frida
Borén, Jan
Bäckhed, Fredrik
author_facet Lindskog Jonsson, Annika
Caesar, Robert
Akrami, Rozita
Reinhardt, Christoph
Fåk Hållenius, Frida
Borén, Jan
Bäckhed, Fredrik
author_sort Lindskog Jonsson, Annika
collection PubMed
description OBJECTIVE—: To investigate the effect of gut microbiota and diet on atherogenesis. APPROACH AND RESULTS—: Here, we investigated the interaction between the gut microbiota and diet on atherosclerosis by feeding germ-free or conventionally raised Apoe(−/−) mice chow or Western diet alone or supplemented with choline (which is metabolized by the gut microbiota and host enzymes to trimethylamine N-oxide) for 12 weeks. We observed smaller aortic lesions and lower plasma cholesterol levels in conventionally raised mice compared with germ-free mice on a chow diet; these differences were not observed in mice on a Western diet. Choline supplementation increased plasma trimethylamine N-oxide levels in conventionally raised mice but not in germ-free mice. However, this treatment did not affect the size of aortic lesions or plasma cholesterol levels. Gut microbiota composition was analyzed by sequencing of 16S rRNA genes. As expected, the global community structure and relative abundance of many taxa differed between mice fed chow or a Western diet. Choline supplementation had minor effects on the community structure although the relative abundance of some taxa belonging to Clostridiales was altered. CONCLUSIONS—: In conclusion, the impact of the gut microbiota on atherosclerosis is dietary dependent and is associated with plasma cholesterol levels. Furthermore, the microbiota was required for trimethylamine N-oxide production from dietary choline, but this process could not be linked to increased atherosclerosis in this model.
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spelling pubmed-61667032018-10-12 Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice Lindskog Jonsson, Annika Caesar, Robert Akrami, Rozita Reinhardt, Christoph Fåk Hållenius, Frida Borén, Jan Bäckhed, Fredrik Arterioscler Thromb Vasc Biol Basic Sciences OBJECTIVE—: To investigate the effect of gut microbiota and diet on atherogenesis. APPROACH AND RESULTS—: Here, we investigated the interaction between the gut microbiota and diet on atherosclerosis by feeding germ-free or conventionally raised Apoe(−/−) mice chow or Western diet alone or supplemented with choline (which is metabolized by the gut microbiota and host enzymes to trimethylamine N-oxide) for 12 weeks. We observed smaller aortic lesions and lower plasma cholesterol levels in conventionally raised mice compared with germ-free mice on a chow diet; these differences were not observed in mice on a Western diet. Choline supplementation increased plasma trimethylamine N-oxide levels in conventionally raised mice but not in germ-free mice. However, this treatment did not affect the size of aortic lesions or plasma cholesterol levels. Gut microbiota composition was analyzed by sequencing of 16S rRNA genes. As expected, the global community structure and relative abundance of many taxa differed between mice fed chow or a Western diet. Choline supplementation had minor effects on the community structure although the relative abundance of some taxa belonging to Clostridiales was altered. CONCLUSIONS—: In conclusion, the impact of the gut microbiota on atherosclerosis is dietary dependent and is associated with plasma cholesterol levels. Furthermore, the microbiota was required for trimethylamine N-oxide production from dietary choline, but this process could not be linked to increased atherosclerosis in this model. Lippincott Williams & Wilkins 2018-10 2018-06-14 /pmc/articles/PMC6166703/ /pubmed/29903735 http://dx.doi.org/10.1161/ATVBAHA.118.311233 Text en © 2018 The Authors. Arteriosclerosis, Thrombosis, and Vascular Biology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Basic Sciences
Lindskog Jonsson, Annika
Caesar, Robert
Akrami, Rozita
Reinhardt, Christoph
Fåk Hållenius, Frida
Borén, Jan
Bäckhed, Fredrik
Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title_full Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title_fullStr Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title_full_unstemmed Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title_short Impact of Gut Microbiota and Diet on the Development of Atherosclerosis in Apoe(−/−) Mice
title_sort impact of gut microbiota and diet on the development of atherosclerosis in apoe(−/−) mice
topic Basic Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166703/
https://www.ncbi.nlm.nih.gov/pubmed/29903735
http://dx.doi.org/10.1161/ATVBAHA.118.311233
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