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
Hauptverfasser: Wielinga, Peter Y., Harthoorn, Lucien F., Verschuren, Lars, Schoemaker, Marieke H., Jouni, Zeina E., van Tol, Eric A.F., Kleemann, Robert, Kooistra, Teake
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container_end_page 1089
container_issue 7
container_start_page 1081
container_title Molecular nutrition & food research
container_volume 56
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
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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 &amp; control ; Hypolipidemic Agents - therapeutic use ; Macrophages - immunology ; Macrophages - pathology ; Male ; Mice ; Mice, Transgenic ; Obesity ; Obesity - blood ; Obesity - immunology ; Obesity - pathology ; Obesity - prevention &amp; 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 &amp; food research, 2012-07, Vol.56 (7), p.1081-1089</ispartof><rights>2012 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2015 INIST-CNRS</rights><rights>2012 WILEY-VCH Verlag GmbH &amp; Co. 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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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