Loading…
Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice
► Enzymatic synthesis of phytosteryl docosahexaneates was successful. ► Structures of phytosteryl docosahexaneates were confirmed by IR and HPLC–MS. ► The phytosteryl docosahexaneates had anti-atherogenic effects in apo-E deficient mice. ► Phytosteryl docosahexaneates may be used as functional foods...
Saved in:
Published in: | Food chemistry 2012-10, Vol.134 (4), p.2097-2104 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43 |
---|---|
cites | cdi_FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43 |
container_end_page | 2104 |
container_issue | 4 |
container_start_page | 2097 |
container_title | Food chemistry |
container_volume | 134 |
creator | Tan, Zhuliang Le, Khuong Moghadasian, Mohammed Shahidi, Fereidoon |
description | ► Enzymatic synthesis of phytosteryl docosahexaneates was successful. ► Structures of phytosteryl docosahexaneates were confirmed by IR and HPLC–MS. ► The phytosteryl docosahexaneates had anti-atherogenic effects in apo-E deficient mice. ► Phytosteryl docosahexaneates may be used as functional foods ingredient/nutraceuticals.
Phytosterols have attracted much attention in recent years due to their health benefits, such as cholesterol lowering, anti-inflammatory, anti-atherogenicity, and anti-cancer potential. Docosahexaenoic acid (DHA) has been demonstrated to possess cardioprotective and immune-enhancing effects. Esterification of phytosterols with DHA may render improved physiochemical properties such as solubility, miscibility, oxidative stability and hence bioactivity and bioavailability. Thus, phytosteryl docosahexaneates (PS-DHA) may offer both the benefits of phytosterols and DHA, possibly in a synergistic manner. Here, we describe a method for enzymatic synthesis of phytosteryl docosahexaneates and evaluation of metabolic and cardiovascular benefits in apo-E deficient (apo E-KO) mice. The structures of phytosteryl docosahexaneates were confirmed by infrared (IR) and high performance liquid chromatography–mass spectrometry (HPLC–MS) using both normal and reverse phase chromatography. Apo E-KO mice were fed with an atherogenic diet containing 2% (w/w) PS-DHA for 7weeks. Plasma lipid levels and the extent and complexity of atherosclerotic lesions were examined and compared with those in the control group. The PS-DHA-treated mice had significantly lower plasma cholesterol levels and three times smaller atherosclerotic lesions in the aortic roots. This pilot study suggests cardiovascular benefits for PS-DHA. Further experimental and clinical studies are needed to confirm such benefits of PS-DHA. |
doi_str_mv | 10.1016/j.foodchem.2012.04.009 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1313425149</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0308814612006462</els_id><sourcerecordid>1313425149</sourcerecordid><originalsourceid>FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43</originalsourceid><addsrcrecordid>eNqFkMFuEzEQhi0EoqHwCpUvSFw2jNfejX0DVQEqVeICZ8trj4mj3XWwnYpFPDyOksKxpxmNvn_G_gi5YbBmwPr3-7WP0dkdTusWWLsGsQZQz8iKyQ1vNrBpn5MVcJCNZKK_Iq9y3gNAZeVLctVyIdq-ZyvyZzv_XiZTgqV5mcsOc8g0enrYLSXmgmkZqYs2ZrPDX2ZGUzBTMzuKD2Y81lycT3gNhlTnJTSm9in-wLmuRO_RlkzDTM0hNlvq0AcbcC50ChZfkxfejBnfXOo1-f5p--32S3P_9fPd7cf7xnIlS8OhN6A8dij44FrLhZJd62TnhRicUCCEHJREzqQynRL9YJw06IbBgQAv-DV5d957SPHnEXPRU8gWx7F-KB6zZpxx0XZMqIr2Z9SmmHNCrw8pTCYtmoE-mdd7_When8xrELqar8Gby43jMKH7F3tUXYG3F8Bka0afzGxD_s91qm9VLyv34cxhNfIQMOl8MmbRhVRlahfDU2_5C0gOp44</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1313425149</pqid></control><display><type>article</type><title>Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice</title><source>Elsevier</source><creator>Tan, Zhuliang ; Le, Khuong ; Moghadasian, Mohammed ; Shahidi, Fereidoon</creator><creatorcontrib>Tan, Zhuliang ; Le, Khuong ; Moghadasian, Mohammed ; Shahidi, Fereidoon</creatorcontrib><description>► Enzymatic synthesis of phytosteryl docosahexaneates was successful. ► Structures of phytosteryl docosahexaneates were confirmed by IR and HPLC–MS. ► The phytosteryl docosahexaneates had anti-atherogenic effects in apo-E deficient mice. ► Phytosteryl docosahexaneates may be used as functional foods ingredient/nutraceuticals.
Phytosterols have attracted much attention in recent years due to their health benefits, such as cholesterol lowering, anti-inflammatory, anti-atherogenicity, and anti-cancer potential. Docosahexaenoic acid (DHA) has been demonstrated to possess cardioprotective and immune-enhancing effects. Esterification of phytosterols with DHA may render improved physiochemical properties such as solubility, miscibility, oxidative stability and hence bioactivity and bioavailability. Thus, phytosteryl docosahexaneates (PS-DHA) may offer both the benefits of phytosterols and DHA, possibly in a synergistic manner. Here, we describe a method for enzymatic synthesis of phytosteryl docosahexaneates and evaluation of metabolic and cardiovascular benefits in apo-E deficient (apo E-KO) mice. The structures of phytosteryl docosahexaneates were confirmed by infrared (IR) and high performance liquid chromatography–mass spectrometry (HPLC–MS) using both normal and reverse phase chromatography. Apo E-KO mice were fed with an atherogenic diet containing 2% (w/w) PS-DHA for 7weeks. Plasma lipid levels and the extent and complexity of atherosclerotic lesions were examined and compared with those in the control group. The PS-DHA-treated mice had significantly lower plasma cholesterol levels and three times smaller atherosclerotic lesions in the aortic roots. This pilot study suggests cardiovascular benefits for PS-DHA. Further experimental and clinical studies are needed to confirm such benefits of PS-DHA.</description><identifier>ISSN: 0308-8146</identifier><identifier>EISSN: 1873-7072</identifier><identifier>DOI: 10.1016/j.foodchem.2012.04.009</identifier><identifier>PMID: 23442661</identifier><identifier>CODEN: FOCHDJ</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Animals ; Apolipoproteins E - deficiency ; Apolipoproteins E - genetics ; Atherosclerosis - drug therapy ; Atherosclerosis - etiology ; Atherosclerosis - metabolism ; Atherosclerosis - prevention & control ; Bioconversions. Hemisynthesis ; Biological and medical sciences ; Biotechnology ; Cholesterol lowering effect ; Diet, Atherogenic - adverse effects ; Docosahexaenoic Acids - administration & dosage ; Docosahexaenoic Acids - chemical synthesis ; Docosahexaenoic Acids - chemistry ; Enzymatic synthesis ; Esterification ; Food industries ; Fundamental and applied biological sciences. Psychology ; Humans ; Lipase - chemistry ; Lipids - blood ; Male ; Methods. Procedures. Technologies ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Molecular Structure ; Phytosterols - administration & dosage ; Phytosterols - chemical synthesis ; Phytosterols - chemistry ; Phytosteryl docosahexaneates</subject><ispartof>Food chemistry, 2012-10, Vol.134 (4), p.2097-2104</ispartof><rights>2012 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43</citedby><cites>FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25962968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23442661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tan, Zhuliang</creatorcontrib><creatorcontrib>Le, Khuong</creatorcontrib><creatorcontrib>Moghadasian, Mohammed</creatorcontrib><creatorcontrib>Shahidi, Fereidoon</creatorcontrib><title>Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice</title><title>Food chemistry</title><addtitle>Food Chem</addtitle><description>► Enzymatic synthesis of phytosteryl docosahexaneates was successful. ► Structures of phytosteryl docosahexaneates were confirmed by IR and HPLC–MS. ► The phytosteryl docosahexaneates had anti-atherogenic effects in apo-E deficient mice. ► Phytosteryl docosahexaneates may be used as functional foods ingredient/nutraceuticals.
Phytosterols have attracted much attention in recent years due to their health benefits, such as cholesterol lowering, anti-inflammatory, anti-atherogenicity, and anti-cancer potential. Docosahexaenoic acid (DHA) has been demonstrated to possess cardioprotective and immune-enhancing effects. Esterification of phytosterols with DHA may render improved physiochemical properties such as solubility, miscibility, oxidative stability and hence bioactivity and bioavailability. Thus, phytosteryl docosahexaneates (PS-DHA) may offer both the benefits of phytosterols and DHA, possibly in a synergistic manner. Here, we describe a method for enzymatic synthesis of phytosteryl docosahexaneates and evaluation of metabolic and cardiovascular benefits in apo-E deficient (apo E-KO) mice. The structures of phytosteryl docosahexaneates were confirmed by infrared (IR) and high performance liquid chromatography–mass spectrometry (HPLC–MS) using both normal and reverse phase chromatography. Apo E-KO mice were fed with an atherogenic diet containing 2% (w/w) PS-DHA for 7weeks. Plasma lipid levels and the extent and complexity of atherosclerotic lesions were examined and compared with those in the control group. The PS-DHA-treated mice had significantly lower plasma cholesterol levels and three times smaller atherosclerotic lesions in the aortic roots. This pilot study suggests cardiovascular benefits for PS-DHA. Further experimental and clinical studies are needed to confirm such benefits of PS-DHA.</description><subject>Animals</subject><subject>Apolipoproteins E - deficiency</subject><subject>Apolipoproteins E - genetics</subject><subject>Atherosclerosis - drug therapy</subject><subject>Atherosclerosis - etiology</subject><subject>Atherosclerosis - metabolism</subject><subject>Atherosclerosis - prevention & control</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cholesterol lowering effect</subject><subject>Diet, Atherogenic - adverse effects</subject><subject>Docosahexaenoic Acids - administration & dosage</subject><subject>Docosahexaenoic Acids - chemical synthesis</subject><subject>Docosahexaenoic Acids - chemistry</subject><subject>Enzymatic synthesis</subject><subject>Esterification</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Lipase - chemistry</subject><subject>Lipids - blood</subject><subject>Male</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Molecular Structure</subject><subject>Phytosterols - administration & dosage</subject><subject>Phytosterols - chemical synthesis</subject><subject>Phytosterols - chemistry</subject><subject>Phytosteryl docosahexaneates</subject><issn>0308-8146</issn><issn>1873-7072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkMFuEzEQhi0EoqHwCpUvSFw2jNfejX0DVQEqVeICZ8trj4mj3XWwnYpFPDyOksKxpxmNvn_G_gi5YbBmwPr3-7WP0dkdTusWWLsGsQZQz8iKyQ1vNrBpn5MVcJCNZKK_Iq9y3gNAZeVLctVyIdq-ZyvyZzv_XiZTgqV5mcsOc8g0enrYLSXmgmkZqYs2ZrPDX2ZGUzBTMzuKD2Y81lycT3gNhlTnJTSm9in-wLmuRO_RlkzDTM0hNlvq0AcbcC50ChZfkxfejBnfXOo1-f5p--32S3P_9fPd7cf7xnIlS8OhN6A8dij44FrLhZJd62TnhRicUCCEHJREzqQynRL9YJw06IbBgQAv-DV5d957SPHnEXPRU8gWx7F-KB6zZpxx0XZMqIr2Z9SmmHNCrw8pTCYtmoE-mdd7_When8xrELqar8Gby43jMKH7F3tUXYG3F8Bka0afzGxD_s91qm9VLyv34cxhNfIQMOl8MmbRhVRlahfDU2_5C0gOp44</recordid><startdate>20121015</startdate><enddate>20121015</enddate><creator>Tan, Zhuliang</creator><creator>Le, Khuong</creator><creator>Moghadasian, Mohammed</creator><creator>Shahidi, Fereidoon</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20121015</creationdate><title>Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice</title><author>Tan, Zhuliang ; Le, Khuong ; Moghadasian, Mohammed ; Shahidi, Fereidoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Apolipoproteins E - deficiency</topic><topic>Apolipoproteins E - genetics</topic><topic>Atherosclerosis - drug therapy</topic><topic>Atherosclerosis - etiology</topic><topic>Atherosclerosis - metabolism</topic><topic>Atherosclerosis - prevention & control</topic><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cholesterol lowering effect</topic><topic>Diet, Atherogenic - adverse effects</topic><topic>Docosahexaenoic Acids - administration & dosage</topic><topic>Docosahexaenoic Acids - chemical synthesis</topic><topic>Docosahexaenoic Acids - chemistry</topic><topic>Enzymatic synthesis</topic><topic>Esterification</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Lipase - chemistry</topic><topic>Lipids - blood</topic><topic>Male</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Molecular Structure</topic><topic>Phytosterols - administration & dosage</topic><topic>Phytosterols - chemical synthesis</topic><topic>Phytosterols - chemistry</topic><topic>Phytosteryl docosahexaneates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, Zhuliang</creatorcontrib><creatorcontrib>Le, Khuong</creatorcontrib><creatorcontrib>Moghadasian, Mohammed</creatorcontrib><creatorcontrib>Shahidi, Fereidoon</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, Zhuliang</au><au>Le, Khuong</au><au>Moghadasian, Mohammed</au><au>Shahidi, Fereidoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice</atitle><jtitle>Food chemistry</jtitle><addtitle>Food Chem</addtitle><date>2012-10-15</date><risdate>2012</risdate><volume>134</volume><issue>4</issue><spage>2097</spage><epage>2104</epage><pages>2097-2104</pages><issn>0308-8146</issn><eissn>1873-7072</eissn><coden>FOCHDJ</coden><abstract>► Enzymatic synthesis of phytosteryl docosahexaneates was successful. ► Structures of phytosteryl docosahexaneates were confirmed by IR and HPLC–MS. ► The phytosteryl docosahexaneates had anti-atherogenic effects in apo-E deficient mice. ► Phytosteryl docosahexaneates may be used as functional foods ingredient/nutraceuticals.
Phytosterols have attracted much attention in recent years due to their health benefits, such as cholesterol lowering, anti-inflammatory, anti-atherogenicity, and anti-cancer potential. Docosahexaenoic acid (DHA) has been demonstrated to possess cardioprotective and immune-enhancing effects. Esterification of phytosterols with DHA may render improved physiochemical properties such as solubility, miscibility, oxidative stability and hence bioactivity and bioavailability. Thus, phytosteryl docosahexaneates (PS-DHA) may offer both the benefits of phytosterols and DHA, possibly in a synergistic manner. Here, we describe a method for enzymatic synthesis of phytosteryl docosahexaneates and evaluation of metabolic and cardiovascular benefits in apo-E deficient (apo E-KO) mice. The structures of phytosteryl docosahexaneates were confirmed by infrared (IR) and high performance liquid chromatography–mass spectrometry (HPLC–MS) using both normal and reverse phase chromatography. Apo E-KO mice were fed with an atherogenic diet containing 2% (w/w) PS-DHA for 7weeks. Plasma lipid levels and the extent and complexity of atherosclerotic lesions were examined and compared with those in the control group. The PS-DHA-treated mice had significantly lower plasma cholesterol levels and three times smaller atherosclerotic lesions in the aortic roots. This pilot study suggests cardiovascular benefits for PS-DHA. Further experimental and clinical studies are needed to confirm such benefits of PS-DHA.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>23442661</pmid><doi>10.1016/j.foodchem.2012.04.009</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0308-8146 |
ispartof | Food chemistry, 2012-10, Vol.134 (4), p.2097-2104 |
issn | 0308-8146 1873-7072 |
language | eng |
recordid | cdi_proquest_miscellaneous_1313425149 |
source | Elsevier |
subjects | Animals Apolipoproteins E - deficiency Apolipoproteins E - genetics Atherosclerosis - drug therapy Atherosclerosis - etiology Atherosclerosis - metabolism Atherosclerosis - prevention & control Bioconversions. Hemisynthesis Biological and medical sciences Biotechnology Cholesterol lowering effect Diet, Atherogenic - adverse effects Docosahexaenoic Acids - administration & dosage Docosahexaenoic Acids - chemical synthesis Docosahexaenoic Acids - chemistry Enzymatic synthesis Esterification Food industries Fundamental and applied biological sciences. Psychology Humans Lipase - chemistry Lipids - blood Male Methods. Procedures. Technologies Mice Mice, Inbred C57BL Mice, Knockout Molecular Structure Phytosterols - administration & dosage Phytosterols - chemical synthesis Phytosterols - chemistry Phytosteryl docosahexaneates |
title | Enzymatic synthesis of phytosteryl docosahexaneates and evaluation of their anti-atherogenic effects in apo-E deficient mice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A31%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Enzymatic%20synthesis%20of%20phytosteryl%20docosahexaneates%20and%20evaluation%20of%20their%20anti-atherogenic%20effects%20in%20apo-E%20deficient%20mice&rft.jtitle=Food%20chemistry&rft.au=Tan,%20Zhuliang&rft.date=2012-10-15&rft.volume=134&rft.issue=4&rft.spage=2097&rft.epage=2104&rft.pages=2097-2104&rft.issn=0308-8146&rft.eissn=1873-7072&rft.coden=FOCHDJ&rft_id=info:doi/10.1016/j.foodchem.2012.04.009&rft_dat=%3Cproquest_cross%3E1313425149%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c398t-306a09fe5e43bd2c349852d85f44bd490448b98e3189a5946bad8aedbbd040f43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1313425149&rft_id=info:pmid/23442661&rfr_iscdi=true |