Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE3Leiden mice
Scope This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden‐transgenic mic...
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Veröffentlicht in: | Molecular nutrition & food research 2012-07, Vol.56 (7), p.1081-1089 |
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creator | Wielinga, Peter Y. Harthoorn, Lucien F. Verschuren, Lars Schoemaker, Marieke H. Jouni, Zeina E. van Tol, Eric A.F. Kleemann, Robert Kooistra, Teake |
description | Scope
This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden‐transgenic mice, a humanized model for hyperlipidemia and mild obesity.
Methods and results
Four‐week‐old male ApoE*3Leiden mice were fed chow diet with or without a mixture of ARA (0.129 wt%) and DHA (0.088 wt%) or Omacor (0.30 wt% EPA, 0.25 wt% DHA). At age 12 weeks, mice were fed high‐fat/high‐carbohydrate (HFHC) diet without above supplements until age 20 weeks. Control mice received chow diet throughout the study. Mice receiving ARA/DHA gained less body weight compared to control and this effect was sustained when fed HFHC. Omacor had no significant effect on body weight gain. Plasma cholesterol and triglycerides were significantly lowered by both supplementations. At 20 weeks, epididymal fat mass was less in ARA/DHA‐supplemented mice, while Omacor had no significant effect on fat mass. Both ARA/DHA and Omacor reduced inguinal adipocyte cell size; only ARA/DHA significantly reduced epididymal macrophage infiltration.
Conclusion
This study shows that early life ARA/DHA, but not Omacor supplementation improves body weight gain later in life. ARA/DHA and to a lesser extent Omacor both improved adipose tissue quality. |
doi_str_mv | 10.1002/mnfr.201100762 |
format | Article |
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This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden‐transgenic mice, a humanized model for hyperlipidemia and mild obesity.
Methods and results
Four‐week‐old male ApoE*3Leiden mice were fed chow diet with or without a mixture of ARA (0.129 wt%) and DHA (0.088 wt%) or Omacor (0.30 wt% EPA, 0.25 wt% DHA). At age 12 weeks, mice were fed high‐fat/high‐carbohydrate (HFHC) diet without above supplements until age 20 weeks. Control mice received chow diet throughout the study. Mice receiving ARA/DHA gained less body weight compared to control and this effect was sustained when fed HFHC. Omacor had no significant effect on body weight gain. Plasma cholesterol and triglycerides were significantly lowered by both supplementations. At 20 weeks, epididymal fat mass was less in ARA/DHA‐supplemented mice, while Omacor had no significant effect on fat mass. Both ARA/DHA and Omacor reduced inguinal adipocyte cell size; only ARA/DHA significantly reduced epididymal macrophage infiltration.
Conclusion
This study shows that early life ARA/DHA, but not Omacor supplementation improves body weight gain later in life. ARA/DHA and to a lesser extent Omacor both improved adipose tissue quality.</description><identifier>ISSN: 1613-4125</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.201100762</identifier><identifier>PMID: 22611002</identifier><language>eng</language><publisher>Weinheim: Blackwell Publishing Ltd</publisher><subject>Adipose Tissue, White - immunology ; Adipose Tissue, White - pathology ; Adiposity ; Animals ; Anti-Obesity Agents - therapeutic use ; ApoE3Leiden mice ; Apolipoprotein E3 - genetics ; Apolipoprotein E3 - metabolism ; Arachidonic Acid - therapeutic use ; Biological and medical sciences ; Cell Size ; Cholesterol - blood ; Dietary Supplements ; Docosahexaenoic Acids - therapeutic use ; Early life ; Feeding. Feeding behavior ; Food industries ; Fundamental and applied biological sciences. Psychology ; Hyperlipidemias - blood ; Hyperlipidemias - immunology ; Hyperlipidemias - pathology ; Hyperlipidemias - prevention & control ; Hypolipidemic Agents - therapeutic use ; Macrophages - immunology ; Macrophages - pathology ; Male ; Mice ; Mice, Transgenic ; Obesity ; Obesity - blood ; Obesity - immunology ; Obesity - pathology ; Obesity - prevention & control ; PUFA ; Specific Pathogen-Free Organisms ; Triglycerides - blood ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Weight Gain</subject><ispartof>Molecular nutrition & food research, 2012-07, Vol.56 (7), p.1081-1089</ispartof><rights>2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2015 INIST-CNRS</rights><rights>2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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.201100762$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmnfr.201100762$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26163404$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22611002$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wielinga, Peter Y.</creatorcontrib><creatorcontrib>Harthoorn, Lucien F.</creatorcontrib><creatorcontrib>Verschuren, Lars</creatorcontrib><creatorcontrib>Schoemaker, Marieke H.</creatorcontrib><creatorcontrib>Jouni, Zeina E.</creatorcontrib><creatorcontrib>van Tol, Eric A.F.</creatorcontrib><creatorcontrib>Kleemann, Robert</creatorcontrib><creatorcontrib>Kooistra, Teake</creatorcontrib><title>Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE3Leiden mice</title><title>Molecular nutrition & food research</title><addtitle>Mol. Nutr. Food Res</addtitle><description>Scope
This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden‐transgenic mice, a humanized model for hyperlipidemia and mild obesity.
Methods and results
Four‐week‐old male ApoE*3Leiden mice were fed chow diet with or without a mixture of ARA (0.129 wt%) and DHA (0.088 wt%) or Omacor (0.30 wt% EPA, 0.25 wt% DHA). At age 12 weeks, mice were fed high‐fat/high‐carbohydrate (HFHC) diet without above supplements until age 20 weeks. Control mice received chow diet throughout the study. Mice receiving ARA/DHA gained less body weight compared to control and this effect was sustained when fed HFHC. Omacor had no significant effect on body weight gain. Plasma cholesterol and triglycerides were significantly lowered by both supplementations. At 20 weeks, epididymal fat mass was less in ARA/DHA‐supplemented mice, while Omacor had no significant effect on fat mass. Both ARA/DHA and Omacor reduced inguinal adipocyte cell size; only ARA/DHA significantly reduced epididymal macrophage infiltration.
Conclusion
This study shows that early life ARA/DHA, but not Omacor supplementation improves body weight gain later in life. ARA/DHA and to a lesser extent Omacor both improved adipose tissue quality.</description><subject>Adipose Tissue, White - immunology</subject><subject>Adipose Tissue, White - pathology</subject><subject>Adiposity</subject><subject>Animals</subject><subject>Anti-Obesity Agents - therapeutic use</subject><subject>ApoE3Leiden mice</subject><subject>Apolipoprotein E3 - genetics</subject><subject>Apolipoprotein E3 - metabolism</subject><subject>Arachidonic Acid - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cell Size</subject><subject>Cholesterol - blood</subject><subject>Dietary Supplements</subject><subject>Docosahexaenoic Acids - therapeutic use</subject><subject>Early life</subject><subject>Feeding. Feeding behavior</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hyperlipidemias - blood</subject><subject>Hyperlipidemias - immunology</subject><subject>Hyperlipidemias - pathology</subject><subject>Hyperlipidemias - prevention & control</subject><subject>Hypolipidemic Agents - therapeutic use</subject><subject>Macrophages - immunology</subject><subject>Macrophages - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Obesity - immunology</subject><subject>Obesity - pathology</subject><subject>Obesity - prevention & control</subject><subject>PUFA</subject><subject>Specific Pathogen-Free Organisms</subject><subject>Triglycerides - blood</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Weight Gain</subject><issn>1613-4125</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUtv1DAUhSMEoqWwZYm8QWLRtH5NHstRH9NK06IiEEvrjn3dMThOaidq82f4rWSUYVjZ9_o75-r6ZNlHRs8Ypfy8CTaeccqmoiz4q-yYFUzkkgnx-nDni6PsXUq_KBWMS_E2O-K82Cn4cfZnGUFvnWmD0wS0M-em1W2CLb4AhnbfzNPQdR4bDD0aYhz2xAWCEP1IvLNIIppBYyKb1ozkGd3jtieP4MIp6TykBiaqcyadEgiGgHFdm1w_7kw89Bhnk6ladu2VWKMzGEjjNL7P3ljwCT_sz5Psx_XV94ubfP11dXuxXOdOFLLKoZagZc1x2ktby9BSURTCVghYVaUuq7qSTG5qRsGUnFthalMVBoXlWJUbcZJ9mX272D4NmHrVuKTRewjYDkkxysVCiLKsJvTTHh02DRrVRddAHNW_P52Az3sAkgZvIwTt0n-uYIWQVE6cnLln53E8vDOqdjZql6w6JKvu7q-_sXl-Pstc6vHlIIP4WxWlKBfq5_1KLVYP9d364VJdir_x_abk</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Wielinga, Peter Y.</creator><creator>Harthoorn, Lucien F.</creator><creator>Verschuren, Lars</creator><creator>Schoemaker, Marieke H.</creator><creator>Jouni, Zeina E.</creator><creator>van Tol, Eric A.F.</creator><creator>Kleemann, Robert</creator><creator>Kooistra, Teake</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201207</creationdate><title>Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE3Leiden mice</title><author>Wielinga, Peter Y. ; Harthoorn, Lucien F. ; Verschuren, Lars ; Schoemaker, Marieke H. ; Jouni, Zeina E. ; van Tol, Eric A.F. ; Kleemann, Robert ; Kooistra, Teake</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3648-a94ac492e261cff1ef03663f8eae887c7898414b910ad722f3d9d86de3f2e87b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adipose Tissue, White - immunology</topic><topic>Adipose Tissue, White - pathology</topic><topic>Adiposity</topic><topic>Animals</topic><topic>Anti-Obesity Agents - therapeutic use</topic><topic>ApoE3Leiden mice</topic><topic>Apolipoprotein E3 - genetics</topic><topic>Apolipoprotein E3 - metabolism</topic><topic>Arachidonic Acid - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cell Size</topic><topic>Cholesterol - blood</topic><topic>Dietary Supplements</topic><topic>Docosahexaenoic Acids - therapeutic use</topic><topic>Early life</topic><topic>Feeding. Feeding behavior</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hyperlipidemias - blood</topic><topic>Hyperlipidemias - immunology</topic><topic>Hyperlipidemias - pathology</topic><topic>Hyperlipidemias - prevention & control</topic><topic>Hypolipidemic Agents - therapeutic use</topic><topic>Macrophages - immunology</topic><topic>Macrophages - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Obesity</topic><topic>Obesity - blood</topic><topic>Obesity - immunology</topic><topic>Obesity - pathology</topic><topic>Obesity - prevention & control</topic><topic>PUFA</topic><topic>Specific Pathogen-Free Organisms</topic><topic>Triglycerides - blood</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Weight Gain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wielinga, Peter Y.</creatorcontrib><creatorcontrib>Harthoorn, Lucien F.</creatorcontrib><creatorcontrib>Verschuren, Lars</creatorcontrib><creatorcontrib>Schoemaker, Marieke H.</creatorcontrib><creatorcontrib>Jouni, Zeina E.</creatorcontrib><creatorcontrib>van Tol, Eric A.F.</creatorcontrib><creatorcontrib>Kleemann, Robert</creatorcontrib><creatorcontrib>Kooistra, Teake</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular nutrition & food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wielinga, Peter Y.</au><au>Harthoorn, Lucien F.</au><au>Verschuren, Lars</au><au>Schoemaker, Marieke H.</au><au>Jouni, Zeina E.</au><au>van Tol, Eric A.F.</au><au>Kleemann, Robert</au><au>Kooistra, Teake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE3Leiden mice</atitle><jtitle>Molecular nutrition & food research</jtitle><addtitle>Mol. Nutr. Food Res</addtitle><date>2012-07</date><risdate>2012</risdate><volume>56</volume><issue>7</issue><spage>1081</spage><epage>1089</epage><pages>1081-1089</pages><issn>1613-4125</issn><eissn>1613-4133</eissn><abstract>Scope
This study addresses whether early life arachidonic acid (ARA)/docosahexaenoic acid (DHA) supplementation or eicosapentaenoic acid (EPA)/DHA (Omacor) supplementation affects body weight gain, lipid metabolism, and adipose tissue quantity and quality in later life in ApoE*3Leiden‐transgenic mice, a humanized model for hyperlipidemia and mild obesity.
Methods and results
Four‐week‐old male ApoE*3Leiden mice were fed chow diet with or without a mixture of ARA (0.129 wt%) and DHA (0.088 wt%) or Omacor (0.30 wt% EPA, 0.25 wt% DHA). At age 12 weeks, mice were fed high‐fat/high‐carbohydrate (HFHC) diet without above supplements until age 20 weeks. Control mice received chow diet throughout the study. Mice receiving ARA/DHA gained less body weight compared to control and this effect was sustained when fed HFHC. Omacor had no significant effect on body weight gain. Plasma cholesterol and triglycerides were significantly lowered by both supplementations. At 20 weeks, epididymal fat mass was less in ARA/DHA‐supplemented mice, while Omacor had no significant effect on fat mass. Both ARA/DHA and Omacor reduced inguinal adipocyte cell size; only ARA/DHA significantly reduced epididymal macrophage infiltration.
Conclusion
This study shows that early life ARA/DHA, but not Omacor supplementation improves body weight gain later in life. ARA/DHA and to a lesser extent Omacor both improved adipose tissue quality.</abstract><cop>Weinheim</cop><pub>Blackwell Publishing Ltd</pub><pmid>22611002</pmid><doi>10.1002/mnfr.201100762</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Tissue, White - immunology Adipose Tissue, White - pathology Adiposity Animals Anti-Obesity Agents - therapeutic use ApoE3Leiden mice Apolipoprotein E3 - genetics Apolipoprotein E3 - metabolism Arachidonic Acid - therapeutic use Biological and medical sciences Cell Size Cholesterol - blood Dietary Supplements Docosahexaenoic Acids - therapeutic use Early life Feeding. Feeding behavior Food industries Fundamental and applied biological sciences. Psychology Hyperlipidemias - blood Hyperlipidemias - immunology Hyperlipidemias - pathology Hyperlipidemias - prevention & control Hypolipidemic Agents - therapeutic use Macrophages - immunology Macrophages - pathology Male Mice Mice, Transgenic Obesity Obesity - blood Obesity - immunology Obesity - pathology Obesity - prevention & control PUFA Specific Pathogen-Free Organisms Triglycerides - blood Vertebrates: anatomy and physiology, studies on body, several organs or systems Weight Gain |
title | Arachidonic acid/docosahexaenoic acid-supplemented diet in early life reduces body weight gain, plasma lipids, and adiposity in later life in ApoE3Leiden mice |
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