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n–3 fatty acids induce oxidative modifications in human erythrocytes depending on dose and duration of dietary supplementation
The present work was performed to study an optimal dose and duration of dietary n-3 polyunsaturated fatty acid (PUFA) supplementation that would not result in harmful modifications of oxidative cell metabolism. Forty healthy subjects were divided into four groups that received 2.5 g/d eicosapentaeno...
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Published in: | The American journal of clinical nutrition 1996-09, Vol.64 (3), p.297-304 |
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description | The present work was performed to study an optimal dose and duration of dietary n-3 polyunsaturated fatty acid (PUFA) supplementation that would not result in harmful modifications of oxidative cell metabolism. Forty healthy subjects were divided into four groups that received 2.5 g/d eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA), 5.1 g EPA + DHA/d, 7.7 g EPA + DHA/d, or placebo. Fatty acid composition, tocopherol status, and susceptibility to lipid peroxidation induced in vitro by 2,2′-azobis-(2-amidinopropane) (AAPH) were evaluated in human red blood cell (RBC) membranes on days 30 and 180. n-3 PUFA treatment increased EPA and DHA concentrations in RBC membranes in a time-dependent manner in all of the n-3 PUFA groups. These modifications occurred with concomitant dose- and time-dependent increases in the membrane unsaturation index. After 30 d of treatment with n-3 PUFAs, alpha-to-copherol significantly increased in RBC membranes of the intermediate- and high-dose groups. Because of the higher concentration of this antioxidant in these groups, the susceptibility of RBC membranes to peroxidation was decreased. However, after 180 d of treatment, alpha-tocopherol decreased to baseline values and AAPH-induced lipid peroxidation increased in a dose-dependent manner. These results show that high doses of dietary n-3 PUFAs, as well as long-time treatments, affect human RBC susceptibility to lipid peroxidation by changes in fatty acid composition and tocopherol content. |
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Forty healthy subjects were divided into four groups that received 2.5 g/d eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA), 5.1 g EPA + DHA/d, 7.7 g EPA + DHA/d, or placebo. Fatty acid composition, tocopherol status, and susceptibility to lipid peroxidation induced in vitro by 2,2′-azobis-(2-amidinopropane) (AAPH) were evaluated in human red blood cell (RBC) membranes on days 30 and 180. n-3 PUFA treatment increased EPA and DHA concentrations in RBC membranes in a time-dependent manner in all of the n-3 PUFA groups. These modifications occurred with concomitant dose- and time-dependent increases in the membrane unsaturation index. After 30 d of treatment with n-3 PUFAs, alpha-to-copherol significantly increased in RBC membranes of the intermediate- and high-dose groups. Because of the higher concentration of this antioxidant in these groups, the susceptibility of RBC membranes to peroxidation was decreased. However, after 180 d of treatment, alpha-tocopherol decreased to baseline values and AAPH-induced lipid peroxidation increased in a dose-dependent manner. These results show that high doses of dietary n-3 PUFAs, as well as long-time treatments, affect human RBC susceptibility to lipid peroxidation by changes in fatty acid composition and tocopherol content.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.1093/ajcn/64.3.297</identifier><identifier>PMID: 8780337</identifier><identifier>CODEN: AJCNAC</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Adult ; Amidines - pharmacology ; Biological and medical sciences ; Blood ; Diet ; Dietary Fats - pharmacology ; Docosahexaenoic Acids - pharmacology ; Dose-Response Relationship, Drug ; Eicosapentaenoic Acid - pharmacology ; Erythrocyte Membrane - drug effects ; Erythrocyte Membrane - metabolism ; Fatty Acids, Omega-3 - blood ; Fatty Acids, Omega-3 - pharmacology ; Feeding. Feeding behavior ; Female ; Food, Fortified ; Fundamental and applied biological sciences. Psychology ; Humans ; Lipid Peroxides - metabolism ; Male ; Middle Aged ; Nutrition ; Oils & fats ; Oxidation ; Oxidation-Reduction ; Time Factors ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vitamin E ; Vitamin E - blood</subject><ispartof>The American journal of clinical nutrition, 1996-09, Vol.64 (3), p.297-304</ispartof><rights>1996 American Society for Nutrition.</rights><rights>1996 INIST-CNRS</rights><rights>Copyright American Society for Clinical Nutrition, Inc. 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Forty healthy subjects were divided into four groups that received 2.5 g/d eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA), 5.1 g EPA + DHA/d, 7.7 g EPA + DHA/d, or placebo. Fatty acid composition, tocopherol status, and susceptibility to lipid peroxidation induced in vitro by 2,2′-azobis-(2-amidinopropane) (AAPH) were evaluated in human red blood cell (RBC) membranes on days 30 and 180. n-3 PUFA treatment increased EPA and DHA concentrations in RBC membranes in a time-dependent manner in all of the n-3 PUFA groups. These modifications occurred with concomitant dose- and time-dependent increases in the membrane unsaturation index. After 30 d of treatment with n-3 PUFAs, alpha-to-copherol significantly increased in RBC membranes of the intermediate- and high-dose groups. Because of the higher concentration of this antioxidant in these groups, the susceptibility of RBC membranes to peroxidation was decreased. However, after 180 d of treatment, alpha-tocopherol decreased to baseline values and AAPH-induced lipid peroxidation increased in a dose-dependent manner. These results show that high doses of dietary n-3 PUFAs, as well as long-time treatments, affect human RBC susceptibility to lipid peroxidation by changes in fatty acid composition and tocopherol content.</description><subject>Adult</subject><subject>Amidines - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Diet</subject><subject>Dietary Fats - pharmacology</subject><subject>Docosahexaenoic Acids - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Eicosapentaenoic Acid - pharmacology</subject><subject>Erythrocyte Membrane - drug effects</subject><subject>Erythrocyte Membrane - metabolism</subject><subject>Fatty Acids, Omega-3 - blood</subject><subject>Fatty Acids, Omega-3 - pharmacology</subject><subject>Feeding. 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Psychology</subject><subject>Humans</subject><subject>Lipid Peroxides - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nutrition</subject><subject>Oils & fats</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Time Factors</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vitamin E</subject><subject>Vitamin E - blood</subject><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp1kctuEzEUhi0EKqGwZIlkIbaT-jIZzyxRVS5SJTawtk6Oz1BHGXuwPRXZ9R14Q54Ep4m6Y2Ud_d-56DNjb6VYSzHoK9hhuOratV6rwTxjKznovtFKmOdsJYRQzSC7zUv2KuedEFK1fXfBLnrTC63Nij2Evw9_NB-hlAMH9C5zH9yCxONv76D4e-JTdH70WIsYjjG_WyYInNKh3KWIh0KZO5opOB9-8hi4i5k4BMfdkh67eBy581QgHXhe5nlPE4XyGL1mL0bYZ3pzfi_Zj08336-_NLffPn-9_njbYDuY0tAWyYxDC-BUp9CBMJ1UqtfSOCPRkDQIiMoIpwTAFjYCpB5og6RHB1t9yd6f5s4p_looF7uLSwp1pVVaDrLf9KZCzQnCFHNONNo5-alebaWwR9v2aNt2rdW22q78u_PQZTuRe6LPemv-4ZxDRtiPCQL6_ITVXxJ9rytmThhVAfeeks3oKSA5nwiLddH_54B_oSefpQ</recordid><startdate>19960901</startdate><enddate>19960901</enddate><creator>Palozza, P</creator><creator>Sgarlata, E</creator><creator>Luberto, C</creator><creator>Piccioni, E</creator><creator>Anti, M</creator><creator>Marra, G</creator><creator>Armelao, F</creator><creator>Franceschelli, P</creator><creator>Bartoli, GM</creator><general>Elsevier Inc</general><general>American Society for Clinical Nutrition</general><general>American Society for Clinical Nutrition, Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>7QP</scope><scope>7T7</scope><scope>7TS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>19960901</creationdate><title>n–3 fatty acids induce oxidative modifications in human erythrocytes depending on dose and duration of dietary supplementation</title><author>Palozza, P ; Sgarlata, E ; Luberto, C ; Piccioni, E ; Anti, M ; Marra, G ; Armelao, F ; Franceschelli, P ; Bartoli, GM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-ebce7f94aad262cda0761228317d71c7e17cacc270d20aaba50a139e5ce3fdab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Amidines - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Diet</topic><topic>Dietary Fats - pharmacology</topic><topic>Docosahexaenoic Acids - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Eicosapentaenoic Acid - pharmacology</topic><topic>Erythrocyte Membrane - drug effects</topic><topic>Erythrocyte Membrane - metabolism</topic><topic>Fatty Acids, Omega-3 - blood</topic><topic>Fatty Acids, Omega-3 - pharmacology</topic><topic>Feeding. 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Forty healthy subjects were divided into four groups that received 2.5 g/d eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA), 5.1 g EPA + DHA/d, 7.7 g EPA + DHA/d, or placebo. Fatty acid composition, tocopherol status, and susceptibility to lipid peroxidation induced in vitro by 2,2′-azobis-(2-amidinopropane) (AAPH) were evaluated in human red blood cell (RBC) membranes on days 30 and 180. n-3 PUFA treatment increased EPA and DHA concentrations in RBC membranes in a time-dependent manner in all of the n-3 PUFA groups. These modifications occurred with concomitant dose- and time-dependent increases in the membrane unsaturation index. After 30 d of treatment with n-3 PUFAs, alpha-to-copherol significantly increased in RBC membranes of the intermediate- and high-dose groups. Because of the higher concentration of this antioxidant in these groups, the susceptibility of RBC membranes to peroxidation was decreased. However, after 180 d of treatment, alpha-tocopherol decreased to baseline values and AAPH-induced lipid peroxidation increased in a dose-dependent manner. These results show that high doses of dietary n-3 PUFAs, as well as long-time treatments, affect human RBC susceptibility to lipid peroxidation by changes in fatty acid composition and tocopherol content.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>8780337</pmid><doi>10.1093/ajcn/64.3.297</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Amidines - pharmacology Biological and medical sciences Blood Diet Dietary Fats - pharmacology Docosahexaenoic Acids - pharmacology Dose-Response Relationship, Drug Eicosapentaenoic Acid - pharmacology Erythrocyte Membrane - drug effects Erythrocyte Membrane - metabolism Fatty Acids, Omega-3 - blood Fatty Acids, Omega-3 - pharmacology Feeding. Feeding behavior Female Food, Fortified Fundamental and applied biological sciences. Psychology Humans Lipid Peroxides - metabolism Male Middle Aged Nutrition Oils & fats Oxidation Oxidation-Reduction Time Factors Vertebrates: anatomy and physiology, studies on body, several organs or systems Vitamin E Vitamin E - blood |
title | n–3 fatty acids induce oxidative modifications in human erythrocytes depending on dose and duration of dietary supplementation |
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