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Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine

BACKGROUND AND AIM: Impaired vasodilatation has been suggested to be caused by inhibition of nitric oxide generation by the recently described asymmetric dimethylarginine (ADMA). In the present study we wanted to explore whether n-3 polyunsaturated fatty acid (PUFA) supplementation and/or diet inter...

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Autores principales: Eid, Hilde MA, Arnesen, Harald, Hjerkinn, Elsa M, Lyberg, Torstein, Ellingsen, Ingrid, Seljeflot, Ingebjørg
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1343562/
https://www.ncbi.nlm.nih.gov/pubmed/16396682
http://dx.doi.org/10.1186/1743-7075-3-4
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author Eid, Hilde MA
Arnesen, Harald
Hjerkinn, Elsa M
Lyberg, Torstein
Ellingsen, Ingrid
Seljeflot, Ingebjørg
author_facet Eid, Hilde MA
Arnesen, Harald
Hjerkinn, Elsa M
Lyberg, Torstein
Ellingsen, Ingrid
Seljeflot, Ingebjørg
author_sort Eid, Hilde MA
collection PubMed
description BACKGROUND AND AIM: Impaired vasodilatation has been suggested to be caused by inhibition of nitric oxide generation by the recently described asymmetric dimethylarginine (ADMA). In the present study we wanted to explore whether n-3 polyunsaturated fatty acid (PUFA) supplementation and/or diet intervention have beneficial influence on endothelial function assessed as plasma levels of ADMA and L-arginine. METHODS: A male population (n = 563, age 70 ± 6 yrs) with long-standing hyperlipidemia, characterized as high risk individuals in 1970–72, was included, randomly allocated to receive placebo n-3 PUFA capsules (corn oil) and no dietary advice (control group), dietary advice (Mediterranean type), n-3 PUFA capsules, or dietary advice and n-3 PUFA combined and followed for 3 years. Fasting blood samples were drawn at baseline and the end of the study. RESULTS: Compliance with both intervention regimens were demonstrated by changes in serum fatty acids and by recordings from a food frequency questionnaire. No influence of either regimens on ADMA levels were obtained. However, n-3 PUFA supplementation was accompanied by a significant increase in L-arginine levels, different from the decrease observed in the placebo group (p < 0.05). In individuals with low body mass index (<26 kg/m(2)), the decrease in L-arginine on placebo was strengthened (p = 0.01), and the L-arginine/ADMA ratio was also significantly reduced (p = 0.04). CONCLUSION: In this rather large randomized intervention study, ADMA levels were not influenced by n-3 PUFA supplementation or dietary counselling. n-3 PUFA did, however, counteract the age-related reduction in L-arginine seen on placebo, especially in lean individuals, which might be discussed as an improvement of endothelial function.
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spelling pubmed-13435622006-01-21 Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine Eid, Hilde MA Arnesen, Harald Hjerkinn, Elsa M Lyberg, Torstein Ellingsen, Ingrid Seljeflot, Ingebjørg Nutr Metab (Lond) Research BACKGROUND AND AIM: Impaired vasodilatation has been suggested to be caused by inhibition of nitric oxide generation by the recently described asymmetric dimethylarginine (ADMA). In the present study we wanted to explore whether n-3 polyunsaturated fatty acid (PUFA) supplementation and/or diet intervention have beneficial influence on endothelial function assessed as plasma levels of ADMA and L-arginine. METHODS: A male population (n = 563, age 70 ± 6 yrs) with long-standing hyperlipidemia, characterized as high risk individuals in 1970–72, was included, randomly allocated to receive placebo n-3 PUFA capsules (corn oil) and no dietary advice (control group), dietary advice (Mediterranean type), n-3 PUFA capsules, or dietary advice and n-3 PUFA combined and followed for 3 years. Fasting blood samples were drawn at baseline and the end of the study. RESULTS: Compliance with both intervention regimens were demonstrated by changes in serum fatty acids and by recordings from a food frequency questionnaire. No influence of either regimens on ADMA levels were obtained. However, n-3 PUFA supplementation was accompanied by a significant increase in L-arginine levels, different from the decrease observed in the placebo group (p < 0.05). In individuals with low body mass index (<26 kg/m(2)), the decrease in L-arginine on placebo was strengthened (p = 0.01), and the L-arginine/ADMA ratio was also significantly reduced (p = 0.04). CONCLUSION: In this rather large randomized intervention study, ADMA levels were not influenced by n-3 PUFA supplementation or dietary counselling. n-3 PUFA did, however, counteract the age-related reduction in L-arginine seen on placebo, especially in lean individuals, which might be discussed as an improvement of endothelial function. BioMed Central 2006-01-05 /pmc/articles/PMC1343562/ /pubmed/16396682 http://dx.doi.org/10.1186/1743-7075-3-4 Text en Copyright © 2006 Eid et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Eid, Hilde MA
Arnesen, Harald
Hjerkinn, Elsa M
Lyberg, Torstein
Ellingsen, Ingrid
Seljeflot, Ingebjørg
Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title_full Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title_fullStr Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title_full_unstemmed Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title_short Effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
title_sort effect of diet and omega-3 fatty acid intervention on asymmetric dimethylarginine
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1343562/
https://www.ncbi.nlm.nih.gov/pubmed/16396682
http://dx.doi.org/10.1186/1743-7075-3-4
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