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Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial

Plant lignans and their microbial metabolites, e.g., enterolactone (ENL), may affect bile acid (BA) metabolism through interaction with hepatic receptors. We evaluated the effects of a flaxseed lignan extract (50 mg/day secoisolariciresinol diglucoside) compared to a placebo for 60 days each on plas...

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Autores principales: Navarro, Sandi L., Levy, Lisa, Curtis, Keith R., Elkon, Isaac, Kahsai, Orsalem J., Ammar, Hamza S., Randolph, Timothy W., Hong, Natalie N., Carnevale Neto, Fausto, Raftery, Daniel, Chapkin, Robert S., Lampe, Johanna W., Hullar, Meredith A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374341/
https://www.ncbi.nlm.nih.gov/pubmed/32575611
http://dx.doi.org/10.3390/nu12061837
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author Navarro, Sandi L.
Levy, Lisa
Curtis, Keith R.
Elkon, Isaac
Kahsai, Orsalem J.
Ammar, Hamza S.
Randolph, Timothy W.
Hong, Natalie N.
Carnevale Neto, Fausto
Raftery, Daniel
Chapkin, Robert S.
Lampe, Johanna W.
Hullar, Meredith A. J.
author_facet Navarro, Sandi L.
Levy, Lisa
Curtis, Keith R.
Elkon, Isaac
Kahsai, Orsalem J.
Ammar, Hamza S.
Randolph, Timothy W.
Hong, Natalie N.
Carnevale Neto, Fausto
Raftery, Daniel
Chapkin, Robert S.
Lampe, Johanna W.
Hullar, Meredith A. J.
author_sort Navarro, Sandi L.
collection PubMed
description Plant lignans and their microbial metabolites, e.g., enterolactone (ENL), may affect bile acid (BA) metabolism through interaction with hepatic receptors. We evaluated the effects of a flaxseed lignan extract (50 mg/day secoisolariciresinol diglucoside) compared to a placebo for 60 days each on plasma BA concentrations in 46 healthy men and women (20–45 years) using samples from a completed randomized, crossover intervention. Twenty BA species were measured in fasting plasma using LC-MS. ENL was measured in 24-h urines by GC-MS. We tested for (a) effects of the intervention on BA concentrations overall and stratified by ENL excretion; and (b) cross-sectional associations between plasma BA and ENL. We also explored the overlap in bacterial metabolism at the genus level and conducted in vitro anaerobic incubations of stool with lignan substrate to identify genes that are enriched in response to lignan metabolism. There were no intervention effects, overall or stratified by ENL at FDR < 0.05. In the cross-sectional analysis, irrespective of treatment, five secondary BAs were associated with ENL excretion (FDR < 0.05). In vitro analyses showed positive associations between ENL production and bacterial gene expression of the bile acid-inducible gene cluster and hydroxysteroid dehydrogenases. These data suggest overlap in community bacterial metabolism of secondary BA and ENL.
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spelling pubmed-73743412020-08-06 Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial Navarro, Sandi L. Levy, Lisa Curtis, Keith R. Elkon, Isaac Kahsai, Orsalem J. Ammar, Hamza S. Randolph, Timothy W. Hong, Natalie N. Carnevale Neto, Fausto Raftery, Daniel Chapkin, Robert S. Lampe, Johanna W. Hullar, Meredith A. J. Nutrients Article Plant lignans and their microbial metabolites, e.g., enterolactone (ENL), may affect bile acid (BA) metabolism through interaction with hepatic receptors. We evaluated the effects of a flaxseed lignan extract (50 mg/day secoisolariciresinol diglucoside) compared to a placebo for 60 days each on plasma BA concentrations in 46 healthy men and women (20–45 years) using samples from a completed randomized, crossover intervention. Twenty BA species were measured in fasting plasma using LC-MS. ENL was measured in 24-h urines by GC-MS. We tested for (a) effects of the intervention on BA concentrations overall and stratified by ENL excretion; and (b) cross-sectional associations between plasma BA and ENL. We also explored the overlap in bacterial metabolism at the genus level and conducted in vitro anaerobic incubations of stool with lignan substrate to identify genes that are enriched in response to lignan metabolism. There were no intervention effects, overall or stratified by ENL at FDR < 0.05. In the cross-sectional analysis, irrespective of treatment, five secondary BAs were associated with ENL excretion (FDR < 0.05). In vitro analyses showed positive associations between ENL production and bacterial gene expression of the bile acid-inducible gene cluster and hydroxysteroid dehydrogenases. These data suggest overlap in community bacterial metabolism of secondary BA and ENL. MDPI 2020-06-19 /pmc/articles/PMC7374341/ /pubmed/32575611 http://dx.doi.org/10.3390/nu12061837 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Navarro, Sandi L.
Levy, Lisa
Curtis, Keith R.
Elkon, Isaac
Kahsai, Orsalem J.
Ammar, Hamza S.
Randolph, Timothy W.
Hong, Natalie N.
Carnevale Neto, Fausto
Raftery, Daniel
Chapkin, Robert S.
Lampe, Johanna W.
Hullar, Meredith A. J.
Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title_full Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title_fullStr Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title_full_unstemmed Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title_short Effect of a Flaxseed Lignan Intervention on Circulating Bile Acids in a Placebo-Controlled Randomized, Crossover Trial
title_sort effect of a flaxseed lignan intervention on circulating bile acids in a placebo-controlled randomized, crossover trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7374341/
https://www.ncbi.nlm.nih.gov/pubmed/32575611
http://dx.doi.org/10.3390/nu12061837
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