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 inMolecular nutrition & food research Vol. 62; no. 20
Main Authors Pignitter, Marc, Lindenmeier, Michael, Andersen, Gaby, Herrfurth, Cornelia, Beermann, Christopher, Schmitt, Joachim J., Feussner, Ivo, Fulda, Martin, Somoza, Veronika
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc 01.10.2018
John Wiley and Sons Inc
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ISSN1613-4125
1613-4133
DOI10.1002/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%.
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
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Snippet Scope 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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmnfr.201800271
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