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Plasmalogen metabolism-related enzymes in rat brain during aging: influence of n-3 fatty acid intake
Plasmalogens (Pls) are phospholipids containing a vinyl–ether bond at the sn-1 position of the glycerol backbone. They represent between 1/2 and 2/3 of the ethanolamine phospholipids in the brain. During aging, the Pls content in human brain falls down. However, the role of Pls metabolism-related en...
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Published in: | Biochimie 2006, Vol.88 (1), p.103-111 |
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description | Plasmalogens (Pls) are phospholipids containing a vinyl–ether bond at the
sn-1 position of the glycerol backbone. They represent between 1/2 and 2/3 of the ethanolamine phospholipids in the brain. During aging, the Pls content in human brain falls down. However, the role of Pls metabolism-related enzymes in the regulation of Pls levels remains to be determined. Dihydroxyacetone phosphate acyltransferase (DHAP-AT) is the enzyme involved in the first step of Pls biosynthesis. In the brain, a phospholipase A
2, which selectively acts on Pls, has been isolated (Pls-PLA
2s). In this work, we aimed to evaluate the impact of DHAP-AT (a key enzyme of Pls biosynthesis) and Pls-PLA
2 (a specific Pls degradation enzyme) on the evolution of Pls content in the rat brain during aging. The influence of n-3 fatty acid intake was also evaluated. Littermates from two generations of n-3 deficient rats were fed an equilibrated diet containing either α-LNA alone or with two doses of DHA. After weaning, 3, 9 or 21 months of diet, rats were sacrificed. Enzymatic assays were performed, Pls levels were assessed and the
sn-2 position of ethanolamine Pls was analyzed. DHAP-AT activity significantly increased between weaning and 3 months with a concomitant increase of brain Pls, which reached maximal levels after 9 months. Then, Pls levels and DHAP-AT activity significantly decreased while Pls-PLA
2s activity significantly increased. Dietary n-3 fatty acids had no effect on DHAP-AT activity and on Pls levels. In conclusion, the increase of brain Pls content in the first part of the life may be related to the high increase of DHAP-AT activity, probably stimulated by DHA. In aged animals, the decrease of Pls levels may mainly be caused to an increase of their degradation by Pls-PLA
2. Dietary DHA may not oppose the physiologic aging. |
doi_str_mv | 10.1016/j.biochi.2005.06.010 |
format | article |
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sn-1 position of the glycerol backbone. They represent between 1/2 and 2/3 of the ethanolamine phospholipids in the brain. During aging, the Pls content in human brain falls down. However, the role of Pls metabolism-related enzymes in the regulation of Pls levels remains to be determined. Dihydroxyacetone phosphate acyltransferase (DHAP-AT) is the enzyme involved in the first step of Pls biosynthesis. In the brain, a phospholipase A
2, which selectively acts on Pls, has been isolated (Pls-PLA
2s). In this work, we aimed to evaluate the impact of DHAP-AT (a key enzyme of Pls biosynthesis) and Pls-PLA
2 (a specific Pls degradation enzyme) on the evolution of Pls content in the rat brain during aging. The influence of n-3 fatty acid intake was also evaluated. Littermates from two generations of n-3 deficient rats were fed an equilibrated diet containing either α-LNA alone or with two doses of DHA. After weaning, 3, 9 or 21 months of diet, rats were sacrificed. Enzymatic assays were performed, Pls levels were assessed and the
sn-2 position of ethanolamine Pls was analyzed. DHAP-AT activity significantly increased between weaning and 3 months with a concomitant increase of brain Pls, which reached maximal levels after 9 months. Then, Pls levels and DHAP-AT activity significantly decreased while Pls-PLA
2s activity significantly increased. Dietary n-3 fatty acids had no effect on DHAP-AT activity and on Pls levels. In conclusion, the increase of brain Pls content in the first part of the life may be related to the high increase of DHAP-AT activity, probably stimulated by DHA. In aged animals, the decrease of Pls levels may mainly be caused to an increase of their degradation by Pls-PLA
2. Dietary DHA may not oppose the physiologic aging.</description><identifier>ISSN: 0300-9084</identifier><identifier>EISSN: 1638-6183</identifier><identifier>DOI: 10.1016/j.biochi.2005.06.010</identifier><identifier>PMID: 16046045</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Acyltransferases - metabolism ; Aging ; Aging - physiology ; Animals ; Biochemistry, Molecular Biology ; Brain ; Brain - enzymology ; Dietary Fats, Unsaturated - pharmacology ; Dihydroxyacetone phosphate acyltransferase ; Docosahexaenoic Acids - pharmacology ; Life Sciences ; Male ; Phospholipase A 2 ; Phospholipases A - metabolism ; Phospholipases A2 ; Plasmalogen ; Plasmalogens - metabolism ; Rats ; Rats, Wistar</subject><ispartof>Biochimie, 2006, Vol.88 (1), p.103-111</ispartof><rights>2005 Elsevier SAS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-90e542238066ccfac4ed741ea527d14ee69ce13758fc8fd1b06131c2b03de1583</citedby><cites>FETCH-LOGICAL-c425t-90e542238066ccfac4ed741ea527d14ee69ce13758fc8fd1b06131c2b03de1583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16046045$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02657082$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>André, A.</creatorcontrib><creatorcontrib>Juanéda, P.</creatorcontrib><creatorcontrib>Sébédio, J.L.</creatorcontrib><creatorcontrib>Chardigny, J.M.</creatorcontrib><title>Plasmalogen metabolism-related enzymes in rat brain during aging: influence of n-3 fatty acid intake</title><title>Biochimie</title><addtitle>Biochimie</addtitle><description>Plasmalogens (Pls) are phospholipids containing a vinyl–ether bond at the
sn-1 position of the glycerol backbone. They represent between 1/2 and 2/3 of the ethanolamine phospholipids in the brain. During aging, the Pls content in human brain falls down. However, the role of Pls metabolism-related enzymes in the regulation of Pls levels remains to be determined. Dihydroxyacetone phosphate acyltransferase (DHAP-AT) is the enzyme involved in the first step of Pls biosynthesis. In the brain, a phospholipase A
2, which selectively acts on Pls, has been isolated (Pls-PLA
2s). In this work, we aimed to evaluate the impact of DHAP-AT (a key enzyme of Pls biosynthesis) and Pls-PLA
2 (a specific Pls degradation enzyme) on the evolution of Pls content in the rat brain during aging. The influence of n-3 fatty acid intake was also evaluated. Littermates from two generations of n-3 deficient rats were fed an equilibrated diet containing either α-LNA alone or with two doses of DHA. After weaning, 3, 9 or 21 months of diet, rats were sacrificed. Enzymatic assays were performed, Pls levels were assessed and the
sn-2 position of ethanolamine Pls was analyzed. DHAP-AT activity significantly increased between weaning and 3 months with a concomitant increase of brain Pls, which reached maximal levels after 9 months. Then, Pls levels and DHAP-AT activity significantly decreased while Pls-PLA
2s activity significantly increased. Dietary n-3 fatty acids had no effect on DHAP-AT activity and on Pls levels. In conclusion, the increase of brain Pls content in the first part of the life may be related to the high increase of DHAP-AT activity, probably stimulated by DHA. In aged animals, the decrease of Pls levels may mainly be caused to an increase of their degradation by Pls-PLA
2. Dietary DHA may not oppose the physiologic aging.</description><subject>Acyltransferases - metabolism</subject><subject>Aging</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Biochemistry, Molecular Biology</subject><subject>Brain</subject><subject>Brain - enzymology</subject><subject>Dietary Fats, Unsaturated - pharmacology</subject><subject>Dihydroxyacetone phosphate acyltransferase</subject><subject>Docosahexaenoic Acids - pharmacology</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Phospholipase A 2</subject><subject>Phospholipases A - metabolism</subject><subject>Phospholipases A2</subject><subject>Plasmalogen</subject><subject>Plasmalogens - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>0300-9084</issn><issn>1638-6183</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkVGL1DAQx4Mo3nr6DUTyJPjQOkmTtOuDcBx6Jyzogz6HNJnuZU3bM0kP1k9vli7nm0KYhJnfTIb_n5DXDGoGTL0_1L2f7Z2vOYCsQdXA4AnZMNV0lWJd85RsoAGottCJC_IipQMUEPj2OblgCkQ5ckPct2DSaMK8x4mOmE0_B5_GKmIwGR3F6fdxxET9RKPJtI-mvNwS_bSnZl_ih1IawoKTRToPdKoaOpicj9RY70otm5_4kjwbTEj46nxfkh-fP32_vq12X2--XF_tKiu4zGVTlILzpgOlrB2MFehawdBI3jomENXWImta2Q22GxzrQbGGWd5D45DJrrkk79a5dybo--hHE496Nl7fXu30KQdcyRY6_sAK-3Zl7-P8a8GU9eiTxRDMhPOSdAusKAf_B3lRWQi5LaBYQRvnlCIOjysw0CfL9EGvlumTZRqULpaVtjfn-Us_ovvbdPaoAB9XAIt0Dx6jTtaf9HY-os3azf7fP_wBZI2oOA</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>André, A.</creator><creator>Juanéda, P.</creator><creator>Sébédio, J.L.</creator><creator>Chardigny, J.M.</creator><general>Elsevier Masson SAS</general><general>Elsevier</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>7TK</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>2006</creationdate><title>Plasmalogen metabolism-related enzymes in rat brain during aging: influence of n-3 fatty acid intake</title><author>André, A. ; Juanéda, P. ; Sébédio, J.L. ; Chardigny, J.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-90e542238066ccfac4ed741ea527d14ee69ce13758fc8fd1b06131c2b03de1583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acyltransferases - metabolism</topic><topic>Aging</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Biochemistry, Molecular Biology</topic><topic>Brain</topic><topic>Brain - enzymology</topic><topic>Dietary Fats, Unsaturated - pharmacology</topic><topic>Dihydroxyacetone phosphate acyltransferase</topic><topic>Docosahexaenoic Acids - pharmacology</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Phospholipase A 2</topic><topic>Phospholipases A - metabolism</topic><topic>Phospholipases A2</topic><topic>Plasmalogen</topic><topic>Plasmalogens - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>André, A.</creatorcontrib><creatorcontrib>Juanéda, P.</creatorcontrib><creatorcontrib>Sébédio, J.L.</creatorcontrib><creatorcontrib>Chardigny, J.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Biochimie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>André, A.</au><au>Juanéda, P.</au><au>Sébédio, J.L.</au><au>Chardigny, J.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasmalogen metabolism-related enzymes in rat brain during aging: influence of n-3 fatty acid intake</atitle><jtitle>Biochimie</jtitle><addtitle>Biochimie</addtitle><date>2006</date><risdate>2006</risdate><volume>88</volume><issue>1</issue><spage>103</spage><epage>111</epage><pages>103-111</pages><issn>0300-9084</issn><eissn>1638-6183</eissn><abstract>Plasmalogens (Pls) are phospholipids containing a vinyl–ether bond at the
sn-1 position of the glycerol backbone. They represent between 1/2 and 2/3 of the ethanolamine phospholipids in the brain. During aging, the Pls content in human brain falls down. However, the role of Pls metabolism-related enzymes in the regulation of Pls levels remains to be determined. Dihydroxyacetone phosphate acyltransferase (DHAP-AT) is the enzyme involved in the first step of Pls biosynthesis. In the brain, a phospholipase A
2, which selectively acts on Pls, has been isolated (Pls-PLA
2s). In this work, we aimed to evaluate the impact of DHAP-AT (a key enzyme of Pls biosynthesis) and Pls-PLA
2 (a specific Pls degradation enzyme) on the evolution of Pls content in the rat brain during aging. The influence of n-3 fatty acid intake was also evaluated. Littermates from two generations of n-3 deficient rats were fed an equilibrated diet containing either α-LNA alone or with two doses of DHA. After weaning, 3, 9 or 21 months of diet, rats were sacrificed. Enzymatic assays were performed, Pls levels were assessed and the
sn-2 position of ethanolamine Pls was analyzed. DHAP-AT activity significantly increased between weaning and 3 months with a concomitant increase of brain Pls, which reached maximal levels after 9 months. Then, Pls levels and DHAP-AT activity significantly decreased while Pls-PLA
2s activity significantly increased. Dietary n-3 fatty acids had no effect on DHAP-AT activity and on Pls levels. In conclusion, the increase of brain Pls content in the first part of the life may be related to the high increase of DHAP-AT activity, probably stimulated by DHA. In aged animals, the decrease of Pls levels may mainly be caused to an increase of their degradation by Pls-PLA
2. Dietary DHA may not oppose the physiologic aging.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>16046045</pmid><doi>10.1016/j.biochi.2005.06.010</doi><tpages>9</tpages></addata></record> |
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subjects | Acyltransferases - metabolism Aging Aging - physiology Animals Biochemistry, Molecular Biology Brain Brain - enzymology Dietary Fats, Unsaturated - pharmacology Dihydroxyacetone phosphate acyltransferase Docosahexaenoic Acids - pharmacology Life Sciences Male Phospholipase A 2 Phospholipases A - metabolism Phospholipases A2 Plasmalogen Plasmalogens - metabolism Rats Rats, Wistar |
title | Plasmalogen metabolism-related enzymes in rat brain during aging: influence of n-3 fatty acid intake |
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