Effect of 1‐ and 2‐Month High‐Dose Alpha‐Linolenic Acid Treatment on 13C‐Labeled Alpha‐Linolenic Acid Incorporation and Conversion in Healthy Subjects
Scope The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA) conversion, and 2) whether ALA incorporation and conversion is saturable after administration of 13C‐labeled ALA‐rich linseed oil (LO). The...
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Published in | Molecular nutrition & food research Vol. 62; no. 20 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc
01.10.2018
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1613-4125 1613-4133 |
DOI | 10.1002/mnfr.201800271 |
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Abstract | Scope
The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA) conversion, and 2) whether ALA incorporation and conversion is saturable after administration of 13C‐labeled ALA‐rich linseed oil (LO). The effect of a daily intake of 7 g nonlabeled LO (>43% w/w ALA) for 1 month after bolus administration of 7 g 13C‐labeled LO on day 1, and for 2 months after bolus administration of 7 g 13C‐labeled LO on day 1 and day 29 on 13C‐ALA incorporation and conversion into its higher homologs is investigated in healthy volunteers.
Methods and results
Incorporation and conversion of LO‐derived 13C‐labeled ALA is quantified by applying compartmental modeling. After bolus administration, a fractional conversion of approximately 30% from 13C‐ALA to 13C‐DHA is calculated as reflected by the LDL compartment. Treatment with LO for 8 weeks induces a mean reduction of 13C‐ALA conversion to 13C‐DHA by 48% as reflected by the LDL compartment, and a mean reduction of the 13C‐ALA incorporation into LDL by 46%.
Conclusion
A 2‐month dietary intake of a high dose of LO is sufficient to reach saturation of ALA incorporation into LDL particles, which are responsible for ALA distribution in the body.
13C‐labeled linseed oil (LO) is used to study the incorporation and conversion of alpha‐linolenic acid in healthy subjects. LDL is identified as the most sensitive compartment compared to plasma phospholipids and erythrocytes to study alpha‐linolenic acid conversion to docosahexaenoic acid. Compartmental modeling reveals a fractional conversion of 30% from 13C‐alpha‐linolenic acid to 13C‐docosahexaenoic acid. Long‐term intake of LO markedly reduces the incorporation of 13C‐alpha‐linolenic acid by 46% and its conversion to 13C‐docosahexaenoic acid by 48%. |
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AbstractList | Scope
The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA) conversion, and 2) whether ALA incorporation and conversion is saturable after administration of 13C‐labeled ALA‐rich linseed oil (LO). The effect of a daily intake of 7 g nonlabeled LO (>43% w/w ALA) for 1 month after bolus administration of 7 g 13C‐labeled LO on day 1, and for 2 months after bolus administration of 7 g 13C‐labeled LO on day 1 and day 29 on 13C‐ALA incorporation and conversion into its higher homologs is investigated in healthy volunteers.
Methods and results
Incorporation and conversion of LO‐derived 13C‐labeled ALA is quantified by applying compartmental modeling. After bolus administration, a fractional conversion of approximately 30% from 13C‐ALA to 13C‐DHA is calculated as reflected by the LDL compartment. Treatment with LO for 8 weeks induces a mean reduction of 13C‐ALA conversion to 13C‐DHA by 48% as reflected by the LDL compartment, and a mean reduction of the 13C‐ALA incorporation into LDL by 46%.
Conclusion
A 2‐month dietary intake of a high dose of LO is sufficient to reach saturation of ALA incorporation into LDL particles, which are responsible for ALA distribution in the body.
13C‐labeled linseed oil (LO) is used to study the incorporation and conversion of alpha‐linolenic acid in healthy subjects. LDL is identified as the most sensitive compartment compared to plasma phospholipids and erythrocytes to study alpha‐linolenic acid conversion to docosahexaenoic acid. Compartmental modeling reveals a fractional conversion of 30% from 13C‐alpha‐linolenic acid to 13C‐docosahexaenoic acid. Long‐term intake of LO markedly reduces the incorporation of 13C‐alpha‐linolenic acid by 46% and its conversion to 13C‐docosahexaenoic acid by 48%. SCOPE: The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA) conversion, and 2) whether ALA incorporation and conversion is saturable after administration of ¹³C‐labeled ALA‐rich linseed oil (LO). The effect of a daily intake of 7 g nonlabeled LO (>43% w/w ALA) for 1 month after bolus administration of 7 g ¹³C‐labeled LO on day 1, and for 2 months after bolus administration of 7 g ¹³C‐labeled LO on day 1 and day 29 on ¹³C‐ALA incorporation and conversion into its higher homologs is investigated in healthy volunteers. METHODS AND RESULTS: Incorporation and conversion of LO‐derived ¹³C‐labeled ALA is quantified by applying compartmental modeling. After bolus administration, a fractional conversion of approximately 30% from ¹³C‐ALA to ¹³C‐DHA is calculated as reflected by the LDL compartment. Treatment with LO for 8 weeks induces a mean reduction of ¹³C‐ALA conversion to ¹³C‐DHA by 48% as reflected by the LDL compartment, and a mean reduction of the ¹³C‐ALA incorporation into LDL by 46%. CONCLUSION: A 2‐month dietary intake of a high dose of LO is sufficient to reach saturation of ALA incorporation into LDL particles, which are responsible for ALA distribution in the body. ScopeThe study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA) conversion, and 2) whether ALA incorporation and conversion is saturable after administration of 13C‐labeled ALA‐rich linseed oil (LO). The effect of a daily intake of 7 g nonlabeled LO (>43% w/w ALA) for 1 month after bolus administration of 7 g 13C‐labeled LO on day 1, and for 2 months after bolus administration of 7 g 13C‐labeled LO on day 1 and day 29 on 13C‐ALA incorporation and conversion into its higher homologs is investigated in healthy volunteers.Methods and resultsIncorporation and conversion of LO‐derived 13C‐labeled ALA is quantified by applying compartmental modeling. After bolus administration, a fractional conversion of approximately 30% from 13C‐ALA to 13C‐DHA is calculated as reflected by the LDL compartment. Treatment with LO for 8 weeks induces a mean reduction of 13C‐ALA conversion to 13C‐DHA by 48% as reflected by the LDL compartment, and a mean reduction of the 13C‐ALA incorporation into LDL by 46%.ConclusionA 2‐month dietary intake of a high dose of LO is sufficient to reach saturation of ALA incorporation into LDL particles, which are responsible for ALA distribution in the body. |
Author | Lindenmeier, Michael Andersen, Gaby Schmitt, Joachim J. Fulda, Martin Herrfurth, Cornelia Pignitter, Marc Somoza, Veronika Beermann, Christopher Feussner, Ivo |
AuthorAffiliation | 3 Department for Plant Biochemistry, Albrecht‐von‐Haller‐Institute for Plant Sciences Georg‐August‐University Goettingen Germany 1 Department of Physiological Chemistry, Faculty of Chemistry University of Vienna Austria 4 Department of Food Technology University of Applied Sciences Fulda Germany 2 German Research Center of Food Chemistry Freising Germany |
AuthorAffiliation_xml | – name: 1 Department of Physiological Chemistry, Faculty of Chemistry University of Vienna Austria – name: 2 German Research Center of Food Chemistry Freising Germany – name: 4 Department of Food Technology University of Applied Sciences Fulda Germany – name: 3 Department for Plant Biochemistry, Albrecht‐von‐Haller‐Institute for Plant Sciences Georg‐August‐University Goettingen Germany |
Author_xml | – sequence: 1 givenname: Marc surname: Pignitter fullname: Pignitter, Marc organization: University of Vienna – sequence: 2 givenname: Michael surname: Lindenmeier fullname: Lindenmeier, Michael organization: German Research Center of Food Chemistry – sequence: 3 givenname: Gaby surname: Andersen fullname: Andersen, Gaby organization: German Research Center of Food Chemistry – sequence: 4 givenname: Cornelia surname: Herrfurth fullname: Herrfurth, Cornelia organization: Georg‐August‐University – sequence: 5 givenname: Christopher surname: Beermann fullname: Beermann, Christopher organization: University of Applied Sciences – sequence: 6 givenname: Joachim J. surname: Schmitt fullname: Schmitt, Joachim J. organization: University of Applied Sciences – sequence: 7 givenname: Ivo surname: Feussner fullname: Feussner, Ivo organization: Georg‐August‐University – sequence: 8 givenname: Martin surname: Fulda fullname: Fulda, Martin organization: Georg‐August‐University – sequence: 9 givenname: Veronika surname: Somoza fullname: Somoza, Veronika email: veronika.somoza@univie.ac.at organization: German Research Center of Food Chemistry |
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The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA)... ScopeThe study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid (ALA)... SCOPE: The study aims at identifying 1) the most sensitive compartment among plasma phospholipids, erythrocytes, and LDL for studying alpha‐linolenic acid... |
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SubjectTerms | acid treatment ALA conversion alpha-linolenic acid carbon Carbon 13 compartment model Conversion Diet Dietary intake Erythrocytes Fish oils food intake Homology isotope labeling LDL Linolenic acid Linseed oil Low density lipoprotein Oils & fats omega‐3 fatty acids Phospholipids Reduction stable isotopes |
Title | Effect of 1‐ and 2‐Month High‐Dose Alpha‐Linolenic Acid Treatment on 13C‐Labeled Alpha‐Linolenic Acid Incorporation and Conversion in Healthy Subjects |
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