Plasma arachidonic acid influences insulin-stimulated glucose uptake in healthy adult women
Background: Fatty acids can modulate lipid metabolism, this is related to insulin resistance (IR). This study evaluated the relationship of plasma fatty acid profile with IR, fuel oxidative metabolism and plasma lipid concentration in ‘healthy’ women. Methods: Sixteen ‘healthy’, sedentary and non-ob...
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Veröffentlicht in: | Annals of nutrition and metabolism 2007-01, Vol.51 (5), p.482-489 |
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description | Background: Fatty acids can modulate lipid metabolism, this is related to insulin resistance (IR). This study evaluated the relationship of plasma fatty acid profile with IR, fuel oxidative metabolism and plasma lipid concentration in ‘healthy’ women. Methods: Sixteen ‘healthy’, sedentary and non-obese women were evaluated under fasting conditions for fuel oxidation, plasma fatty acid profile, free fatty acids, triglycerides, glucose and insulin concentrations. IR, fuel oxidation and plasma lipids were measured under insulin-stimulated conditions. Using the Spearman test the correlation between relevant variables was assessed. Stepwise multiple regression analysis was done to identify the main clinical/metabolic and fatty acid determinants of IR. Results: Plasma arachidonic acid content (%) determined IR, and in combination with insulin-stimulated plasma triglyceride concentration explained 45% of the IR variance. IR was inversely related to physical fitness (rs = –0.48, p = 0.01). The latter was inversely associated to plasma saturated fatty acid content (%) (rs = –0.48, p < 0.01), but directly associated to plasma docosahexaenoic acid content (%) (rs = 0.40, p = 0.04). Conclusions: Support for the hypothesis that specific fatty acids influence IR is provided. Plasma arachidonic acid was associated to IR, independent on clinical/metabolic study variables. Docosahexaenoic and saturated fatty acids could potentially affect insulin action through modulating mitochondrial oxidative function. |
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This study evaluated the relationship of plasma fatty acid profile with IR, fuel oxidative metabolism and plasma lipid concentration in ‘healthy’ women. Methods: Sixteen ‘healthy’, sedentary and non-obese women were evaluated under fasting conditions for fuel oxidation, plasma fatty acid profile, free fatty acids, triglycerides, glucose and insulin concentrations. IR, fuel oxidation and plasma lipids were measured under insulin-stimulated conditions. Using the Spearman test the correlation between relevant variables was assessed. Stepwise multiple regression analysis was done to identify the main clinical/metabolic and fatty acid determinants of IR. Results: Plasma arachidonic acid content (%) determined IR, and in combination with insulin-stimulated plasma triglyceride concentration explained 45% of the IR variance. IR was inversely related to physical fitness (rs = –0.48, p = 0.01). The latter was inversely associated to plasma saturated fatty acid content (%) (rs = –0.48, p < 0.01), but directly associated to plasma docosahexaenoic acid content (%) (rs = 0.40, p = 0.04). Conclusions: Support for the hypothesis that specific fatty acids influence IR is provided. Plasma arachidonic acid was associated to IR, independent on clinical/metabolic study variables. Docosahexaenoic and saturated fatty acids could potentially affect insulin action through modulating mitochondrial oxidative function.</description><identifier>ISSN: 0250-6807</identifier><identifier>EISSN: 1421-9697</identifier><identifier>DOI: 10.1159/000111171</identifier><identifier>PMID: 18025824</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adult ; adults ; arachidonic acid ; Arachidonic Acid - administration & dosage ; Arachidonic Acid - blood ; blood chemistry ; blood glucose ; Blood Glucose - metabolism ; blood lipids ; docosahexaenoic acid ; fatty acid composition ; Fatty acids ; Female ; Glucose ; Humans ; Insulin ; Insulin - metabolism ; Insulin Resistance ; lipid metabolism ; Lipids ; Metabolism ; Mitochondria - drug effects ; Mitochondria - metabolism ; Nutrition ; Original Paper ; Oxidation ; Physical Fitness ; saturated fatty acids ; Women</subject><ispartof>Annals of nutrition and metabolism, 2007-01, Vol.51 (5), p.482-489</ispartof><rights>2007 S. Karger AG</rights><rights>2007 S. Karger AG, Basel</rights><rights>(c) 2007 S. Karger AG, Basel.</rights><rights>Copyright (c) 2007 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-7913b1a409b771bc11bc6b47da0431b7061a92133d27f87bf3dadd9cbb5eb0e83</citedby><cites>FETCH-LOGICAL-c377t-7913b1a409b771bc11bc6b47da0431b7061a92133d27f87bf3dadd9cbb5eb0e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/48507533$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/48507533$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,2422,27903,27904,57995,58228</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18025824$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Galgani, José E.</creatorcontrib><creatorcontrib>Aguirre, Carolina A.</creatorcontrib><creatorcontrib>Uauy, Ricardo D.</creatorcontrib><creatorcontrib>Díaz, Erik O.</creatorcontrib><title>Plasma arachidonic acid influences insulin-stimulated glucose uptake in healthy adult women</title><title>Annals of nutrition and metabolism</title><addtitle>Ann Nutr Metab</addtitle><description>Background: Fatty acids can modulate lipid metabolism, this is related to insulin resistance (IR). This study evaluated the relationship of plasma fatty acid profile with IR, fuel oxidative metabolism and plasma lipid concentration in ‘healthy’ women. Methods: Sixteen ‘healthy’, sedentary and non-obese women were evaluated under fasting conditions for fuel oxidation, plasma fatty acid profile, free fatty acids, triglycerides, glucose and insulin concentrations. IR, fuel oxidation and plasma lipids were measured under insulin-stimulated conditions. Using the Spearman test the correlation between relevant variables was assessed. Stepwise multiple regression analysis was done to identify the main clinical/metabolic and fatty acid determinants of IR. Results: Plasma arachidonic acid content (%) determined IR, and in combination with insulin-stimulated plasma triglyceride concentration explained 45% of the IR variance. IR was inversely related to physical fitness (rs = –0.48, p = 0.01). The latter was inversely associated to plasma saturated fatty acid content (%) (rs = –0.48, p < 0.01), but directly associated to plasma docosahexaenoic acid content (%) (rs = 0.40, p = 0.04). Conclusions: Support for the hypothesis that specific fatty acids influence IR is provided. Plasma arachidonic acid was associated to IR, independent on clinical/metabolic study variables. Docosahexaenoic and saturated fatty acids could potentially affect insulin action through modulating mitochondrial oxidative function.</description><subject>Adult</subject><subject>adults</subject><subject>arachidonic acid</subject><subject>Arachidonic Acid - administration & dosage</subject><subject>Arachidonic Acid - blood</subject><subject>blood chemistry</subject><subject>blood glucose</subject><subject>Blood Glucose - metabolism</subject><subject>blood lipids</subject><subject>docosahexaenoic acid</subject><subject>fatty acid composition</subject><subject>Fatty acids</subject><subject>Female</subject><subject>Glucose</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin Resistance</subject><subject>lipid metabolism</subject><subject>Lipids</subject><subject>Metabolism</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Nutrition</subject><subject>Original Paper</subject><subject>Oxidation</subject><subject>Physical Fitness</subject><subject>saturated fatty acids</subject><subject>Women</subject><issn>0250-6807</issn><issn>1421-9697</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpd0M1rFDEYBvAgil2rB-9-DB4ED6P5mknmKKVVoaCgPXkIbz5mN9vMZJtMkP73RmZ1wUBI4PnlJTwIPSf4PSHd8AFjTOoS5AHaEE5JO_SDeIg2mHa47SUWZ-hJzvuqqOTdY3RGZI0k5Rv081uAPEEDCczO2zh704DxtvHzGIqbjcv1mkvwc5sXP5UAi7PNNhQTs2vKYYFbV0WzcxCW3X0DtoSl-RUnNz9Fj0YI2T07nufo5uryx8Xn9vrrpy8XH69bw4RYWjEQpglwPGghiDak7l5zYQFzRrTAPYGBEsYsFaMUemQWrB2M1p3T2El2jt6ucw8p3hWXFzX5bFwIMLtYsuoHzBinXYVv_oP7WNJc_6Yoo1gw2dOK3q3IpJhzcqM6JD9BulcEqz91q391V_vqOLDoydmTPPZbwYsV3ELaunQCf9-_XON9XuIp5bLDomOs5q_XfISoYJt8VjffKSYMYym5rKX8Bj7rlfU</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Galgani, José E.</creator><creator>Aguirre, Carolina A.</creator><creator>Uauy, Ricardo D.</creator><creator>Díaz, Erik O.</creator><general>S. Karger AG</general><scope>FBQ</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0K</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20070101</creationdate><title>Plasma arachidonic acid influences insulin-stimulated glucose uptake in healthy adult women</title><author>Galgani, José E. ; Aguirre, Carolina A. ; Uauy, Ricardo D. ; Díaz, Erik O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-7913b1a409b771bc11bc6b47da0431b7061a92133d27f87bf3dadd9cbb5eb0e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>adults</topic><topic>arachidonic acid</topic><topic>Arachidonic Acid - administration & dosage</topic><topic>Arachidonic Acid - blood</topic><topic>blood chemistry</topic><topic>blood glucose</topic><topic>Blood Glucose - metabolism</topic><topic>blood lipids</topic><topic>docosahexaenoic acid</topic><topic>fatty acid composition</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Glucose</topic><topic>Humans</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Insulin Resistance</topic><topic>lipid metabolism</topic><topic>Lipids</topic><topic>Metabolism</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Nutrition</topic><topic>Original Paper</topic><topic>Oxidation</topic><topic>Physical Fitness</topic><topic>saturated fatty acids</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Galgani, José E.</creatorcontrib><creatorcontrib>Aguirre, Carolina A.</creatorcontrib><creatorcontrib>Uauy, Ricardo D.</creatorcontrib><creatorcontrib>Díaz, Erik O.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of nutrition and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Galgani, José E.</au><au>Aguirre, Carolina A.</au><au>Uauy, Ricardo D.</au><au>Díaz, Erik O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma arachidonic acid influences insulin-stimulated glucose uptake in healthy adult women</atitle><jtitle>Annals of nutrition and metabolism</jtitle><addtitle>Ann Nutr Metab</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>51</volume><issue>5</issue><spage>482</spage><epage>489</epage><pages>482-489</pages><issn>0250-6807</issn><eissn>1421-9697</eissn><abstract>Background: Fatty acids can modulate lipid metabolism, this is related to insulin resistance (IR). This study evaluated the relationship of plasma fatty acid profile with IR, fuel oxidative metabolism and plasma lipid concentration in ‘healthy’ women. Methods: Sixteen ‘healthy’, sedentary and non-obese women were evaluated under fasting conditions for fuel oxidation, plasma fatty acid profile, free fatty acids, triglycerides, glucose and insulin concentrations. IR, fuel oxidation and plasma lipids were measured under insulin-stimulated conditions. Using the Spearman test the correlation between relevant variables was assessed. Stepwise multiple regression analysis was done to identify the main clinical/metabolic and fatty acid determinants of IR. Results: Plasma arachidonic acid content (%) determined IR, and in combination with insulin-stimulated plasma triglyceride concentration explained 45% of the IR variance. IR was inversely related to physical fitness (rs = –0.48, p = 0.01). The latter was inversely associated to plasma saturated fatty acid content (%) (rs = –0.48, p < 0.01), but directly associated to plasma docosahexaenoic acid content (%) (rs = 0.40, p = 0.04). Conclusions: Support for the hypothesis that specific fatty acids influence IR is provided. Plasma arachidonic acid was associated to IR, independent on clinical/metabolic study variables. Docosahexaenoic and saturated fatty acids could potentially affect insulin action through modulating mitochondrial oxidative function.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>18025824</pmid><doi>10.1159/000111171</doi><tpages>8</tpages></addata></record> |
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subjects | Adult adults arachidonic acid Arachidonic Acid - administration & dosage Arachidonic Acid - blood blood chemistry blood glucose Blood Glucose - metabolism blood lipids docosahexaenoic acid fatty acid composition Fatty acids Female Glucose Humans Insulin Insulin - metabolism Insulin Resistance lipid metabolism Lipids Metabolism Mitochondria - drug effects Mitochondria - metabolism Nutrition Original Paper Oxidation Physical Fitness saturated fatty acids Women |
title | Plasma arachidonic acid influences insulin-stimulated glucose uptake in healthy adult women |
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