Effect of Diets on Plasma and Aorta Lipidome: A Study in the apoE Knockout Mouse Model
Scope Specific lipid molecules circulating in plasma at low concentrations have emerged as biomarkers of atherosclerotic risk. The aim of the present study is that of evaluating, in an athero‐prone mouse model, how different diets can affect plasma and aorta lipidome. Methods and results Thirty‐six...
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Veröffentlicht in: | Molecular nutrition & food research 2023-01, Vol.67 (2), p.e2200367-n/a |
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description | Scope
Specific lipid molecules circulating in plasma at low concentrations have emerged as biomarkers of atherosclerotic risk. The aim of the present study is that of evaluating, in an athero‐prone mouse model, how different diets can affect plasma and aorta lipidome.
Methods and results
Thirty‐six apoE knockout mice are divided in three groups and feed 12 weeks with diets differing for cholesterol and fatty acid content. Atherosclerosis is measured at the aortic sinus and aorta. Lipids are quantified in plasma and aorta with mass spectrometry. The cholesterol content of the diets is the main driver of lipid accumulation in plasma and aorta. The fatty acid composition of the diets affects plasma levels both of essential (linoleic acid) and nonessential (myristic and arachidonic acid) ones. Lipidomics show a comparable distribution, in plasma and aorta, of the main lipid components of oxidized LDL, including cholesteryl esters and lysophosphatidylcholines. Interestingly, lactosylceramide, glucosyl/galactosylceramide, and individual ceramide species are found to accumulate in diseased aortic segments.
Conclusion
Both the cholesterol and fatty acid content of the diets profoundly affect plasma lipidome. Aorta lipidome is likewise affected with the accumulation of specific lipids known as markers of atherosclerosis.
This study investigates, in atherosclerosis‐prone mice, how diets with different lipid contents can affect the amount and composition of lipids in plasma and atherosclerotic plaques. The study demonstrates that dietary cholesterol and fatty acid composition strongly affect plasma and aortic lipidome of mice. That should be carefully considered when running studies aimed at looking for lipid biomarkers of disease. |
doi_str_mv | 10.1002/mnfr.202200367 |
format | Article |
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Specific lipid molecules circulating in plasma at low concentrations have emerged as biomarkers of atherosclerotic risk. The aim of the present study is that of evaluating, in an athero‐prone mouse model, how different diets can affect plasma and aorta lipidome.
Methods and results
Thirty‐six apoE knockout mice are divided in three groups and feed 12 weeks with diets differing for cholesterol and fatty acid content. Atherosclerosis is measured at the aortic sinus and aorta. Lipids are quantified in plasma and aorta with mass spectrometry. The cholesterol content of the diets is the main driver of lipid accumulation in plasma and aorta. The fatty acid composition of the diets affects plasma levels both of essential (linoleic acid) and nonessential (myristic and arachidonic acid) ones. Lipidomics show a comparable distribution, in plasma and aorta, of the main lipid components of oxidized LDL, including cholesteryl esters and lysophosphatidylcholines. Interestingly, lactosylceramide, glucosyl/galactosylceramide, and individual ceramide species are found to accumulate in diseased aortic segments.
Conclusion
Both the cholesterol and fatty acid content of the diets profoundly affect plasma lipidome. Aorta lipidome is likewise affected with the accumulation of specific lipids known as markers of atherosclerosis.
This study investigates, in atherosclerosis‐prone mice, how diets with different lipid contents can affect the amount and composition of lipids in plasma and atherosclerotic plaques. The study demonstrates that dietary cholesterol and fatty acid composition strongly affect plasma and aortic lipidome of mice. That should be carefully considered when running studies aimed at looking for lipid biomarkers of disease.</description><identifier>ISSN: 1613-4125</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.202200367</identifier><identifier>PMID: 36419336</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Accumulation ; Animals ; Aorta ; Aorta - metabolism ; Apolipoprotein E ; Apolipoproteins E - genetics ; Arachidonic acid ; Arteriosclerosis ; Atherosclerosis ; Atherosclerosis - blood ; Atherosclerosis - metabolism ; Biomarkers ; Biomarkers - blood ; Biomarkers - metabolism ; Ceramide ; Cholesterol ; Cholesterol, Dietary - blood ; Cholesterol, Dietary - metabolism ; Coronary vessels ; Diet ; Esters ; Fatty acid composition ; Fatty acids ; Fatty Acids - blood ; Fatty Acids - metabolism ; Galactosylceramide ; Linoleic acid ; Lipidomics ; Lipids ; Low concentrations ; Low density lipoprotein ; Mass spectrometry ; Mass spectroscopy ; Mice ; Mice, Knockout ; mouse models ; Plasma ; Plasma levels</subject><ispartof>Molecular nutrition & food research, 2023-01, Vol.67 (2), p.e2200367-n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><rights>2022 Wiley-VCH GmbH.</rights><rights>2023 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2987-1063fc38ed8e3c91162baf301a8664cc0346834217e93b76f12c8ca69571ca953</citedby><cites>FETCH-LOGICAL-c2987-1063fc38ed8e3c91162baf301a8664cc0346834217e93b76f12c8ca69571ca953</cites><orcidid>0000-0003-3245-2872 ; 0000-0002-1232-2635</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmnfr.202200367$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmnfr.202200367$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36419336$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Busnelli, Marco</creatorcontrib><creatorcontrib>Manzini, Stefano</creatorcontrib><creatorcontrib>Colombo, Alice</creatorcontrib><creatorcontrib>Franchi, Elsa</creatorcontrib><creatorcontrib>Lääperi, Mitja</creatorcontrib><creatorcontrib>Laaksonen, Reijo</creatorcontrib><creatorcontrib>Chiesa, Giulia</creatorcontrib><title>Effect of Diets on Plasma and Aorta Lipidome: A Study in the apoE Knockout Mouse Model</title><title>Molecular nutrition & food research</title><addtitle>Mol Nutr Food Res</addtitle><description>Scope
Specific lipid molecules circulating in plasma at low concentrations have emerged as biomarkers of atherosclerotic risk. The aim of the present study is that of evaluating, in an athero‐prone mouse model, how different diets can affect plasma and aorta lipidome.
Methods and results
Thirty‐six apoE knockout mice are divided in three groups and feed 12 weeks with diets differing for cholesterol and fatty acid content. Atherosclerosis is measured at the aortic sinus and aorta. Lipids are quantified in plasma and aorta with mass spectrometry. The cholesterol content of the diets is the main driver of lipid accumulation in plasma and aorta. The fatty acid composition of the diets affects plasma levels both of essential (linoleic acid) and nonessential (myristic and arachidonic acid) ones. Lipidomics show a comparable distribution, in plasma and aorta, of the main lipid components of oxidized LDL, including cholesteryl esters and lysophosphatidylcholines. Interestingly, lactosylceramide, glucosyl/galactosylceramide, and individual ceramide species are found to accumulate in diseased aortic segments.
Conclusion
Both the cholesterol and fatty acid content of the diets profoundly affect plasma lipidome. Aorta lipidome is likewise affected with the accumulation of specific lipids known as markers of atherosclerosis.
This study investigates, in atherosclerosis‐prone mice, how diets with different lipid contents can affect the amount and composition of lipids in plasma and atherosclerotic plaques. The study demonstrates that dietary cholesterol and fatty acid composition strongly affect plasma and aortic lipidome of mice. That should be carefully considered when running studies aimed at looking for lipid biomarkers of disease.</description><subject>Accumulation</subject><subject>Animals</subject><subject>Aorta</subject><subject>Aorta - metabolism</subject><subject>Apolipoprotein E</subject><subject>Apolipoproteins E - genetics</subject><subject>Arachidonic acid</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - blood</subject><subject>Atherosclerosis - metabolism</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - metabolism</subject><subject>Ceramide</subject><subject>Cholesterol</subject><subject>Cholesterol, Dietary - blood</subject><subject>Cholesterol, Dietary - metabolism</subject><subject>Coronary vessels</subject><subject>Diet</subject><subject>Esters</subject><subject>Fatty acid composition</subject><subject>Fatty acids</subject><subject>Fatty Acids - blood</subject><subject>Fatty Acids - metabolism</subject><subject>Galactosylceramide</subject><subject>Linoleic acid</subject><subject>Lipidomics</subject><subject>Lipids</subject><subject>Low concentrations</subject><subject>Low density lipoprotein</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>mouse models</subject><subject>Plasma</subject><subject>Plasma levels</subject><issn>1613-4125</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0D1PwzAQBmALgWgprIzIEgtLiu1z7IStKi0gWkB8rZHr2CIliUOcCPXfk6qlAwvL-YbHr04vQqeUDCkh7LIobT1khDFCQMg91KeCQsApwP5uZ2EPHXm_7AhlHA5RDwSnMYDoo_eJtUY32Fl8nZnGY1fip1z5QmFVpnjk6kbhWVZlqSvMFR7hl6ZNVzgrcfNhsKrcBN-XTn-6tsFz13rTzdTkx-jAqtybk-07QG_Tyev4Npg93tyNR7NAsziSASUCrIbIpJEBHVMq2EJZIFRFQnCtCXARAWdUmhgWUljKdKSViENJtYpDGKCLTW5Vu6_W-CYpMq9NnqvSdNckTEIsORC-pud_6NK1ddld1ykhQQKDqFPDjdK18742NqnqrFD1KqEkWTeerBtPdo13H862se2iMOmO_1bcAb4B31luVv_EJfOH6TOHUMIP7T2IuA</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Busnelli, Marco</creator><creator>Manzini, Stefano</creator><creator>Colombo, Alice</creator><creator>Franchi, Elsa</creator><creator>Lääperi, Mitja</creator><creator>Laaksonen, Reijo</creator><creator>Chiesa, Giulia</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3245-2872</orcidid><orcidid>https://orcid.org/0000-0002-1232-2635</orcidid></search><sort><creationdate>202301</creationdate><title>Effect of Diets on Plasma and Aorta Lipidome: A Study in the apoE Knockout Mouse Model</title><author>Busnelli, Marco ; Manzini, Stefano ; Colombo, Alice ; Franchi, Elsa ; Lääperi, Mitja ; Laaksonen, Reijo ; Chiesa, Giulia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2987-1063fc38ed8e3c91162baf301a8664cc0346834217e93b76f12c8ca69571ca953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Accumulation</topic><topic>Animals</topic><topic>Aorta</topic><topic>Aorta - metabolism</topic><topic>Apolipoprotein E</topic><topic>Apolipoproteins E - genetics</topic><topic>Arachidonic acid</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - blood</topic><topic>Atherosclerosis - metabolism</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - metabolism</topic><topic>Ceramide</topic><topic>Cholesterol</topic><topic>Cholesterol, Dietary - blood</topic><topic>Cholesterol, Dietary - metabolism</topic><topic>Coronary vessels</topic><topic>Diet</topic><topic>Esters</topic><topic>Fatty acid composition</topic><topic>Fatty acids</topic><topic>Fatty Acids - blood</topic><topic>Fatty Acids - metabolism</topic><topic>Galactosylceramide</topic><topic>Linoleic acid</topic><topic>Lipidomics</topic><topic>Lipids</topic><topic>Low concentrations</topic><topic>Low density lipoprotein</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>mouse models</topic><topic>Plasma</topic><topic>Plasma levels</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Busnelli, Marco</creatorcontrib><creatorcontrib>Manzini, Stefano</creatorcontrib><creatorcontrib>Colombo, Alice</creatorcontrib><creatorcontrib>Franchi, Elsa</creatorcontrib><creatorcontrib>Lääperi, Mitja</creatorcontrib><creatorcontrib>Laaksonen, Reijo</creatorcontrib><creatorcontrib>Chiesa, Giulia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular nutrition & food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Busnelli, Marco</au><au>Manzini, Stefano</au><au>Colombo, Alice</au><au>Franchi, Elsa</au><au>Lääperi, Mitja</au><au>Laaksonen, Reijo</au><au>Chiesa, Giulia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Diets on Plasma and Aorta Lipidome: A Study in the apoE Knockout Mouse Model</atitle><jtitle>Molecular nutrition & food research</jtitle><addtitle>Mol Nutr Food Res</addtitle><date>2023-01</date><risdate>2023</risdate><volume>67</volume><issue>2</issue><spage>e2200367</spage><epage>n/a</epage><pages>e2200367-n/a</pages><issn>1613-4125</issn><eissn>1613-4133</eissn><abstract>Scope
Specific lipid molecules circulating in plasma at low concentrations have emerged as biomarkers of atherosclerotic risk. The aim of the present study is that of evaluating, in an athero‐prone mouse model, how different diets can affect plasma and aorta lipidome.
Methods and results
Thirty‐six apoE knockout mice are divided in three groups and feed 12 weeks with diets differing for cholesterol and fatty acid content. Atherosclerosis is measured at the aortic sinus and aorta. Lipids are quantified in plasma and aorta with mass spectrometry. The cholesterol content of the diets is the main driver of lipid accumulation in plasma and aorta. The fatty acid composition of the diets affects plasma levels both of essential (linoleic acid) and nonessential (myristic and arachidonic acid) ones. Lipidomics show a comparable distribution, in plasma and aorta, of the main lipid components of oxidized LDL, including cholesteryl esters and lysophosphatidylcholines. Interestingly, lactosylceramide, glucosyl/galactosylceramide, and individual ceramide species are found to accumulate in diseased aortic segments.
Conclusion
Both the cholesterol and fatty acid content of the diets profoundly affect plasma lipidome. Aorta lipidome is likewise affected with the accumulation of specific lipids known as markers of atherosclerosis.
This study investigates, in atherosclerosis‐prone mice, how diets with different lipid contents can affect the amount and composition of lipids in plasma and atherosclerotic plaques. The study demonstrates that dietary cholesterol and fatty acid composition strongly affect plasma and aortic lipidome of mice. That should be carefully considered when running studies aimed at looking for lipid biomarkers of disease.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36419336</pmid><doi>10.1002/mnfr.202200367</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-3245-2872</orcidid><orcidid>https://orcid.org/0000-0002-1232-2635</orcidid></addata></record> |
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subjects | Accumulation Animals Aorta Aorta - metabolism Apolipoprotein E Apolipoproteins E - genetics Arachidonic acid Arteriosclerosis Atherosclerosis Atherosclerosis - blood Atherosclerosis - metabolism Biomarkers Biomarkers - blood Biomarkers - metabolism Ceramide Cholesterol Cholesterol, Dietary - blood Cholesterol, Dietary - metabolism Coronary vessels Diet Esters Fatty acid composition Fatty acids Fatty Acids - blood Fatty Acids - metabolism Galactosylceramide Linoleic acid Lipidomics Lipids Low concentrations Low density lipoprotein Mass spectrometry Mass spectroscopy Mice Mice, Knockout mouse models Plasma Plasma levels |
title | Effect of Diets on Plasma and Aorta Lipidome: A Study in the apoE Knockout Mouse Model |
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