β-Carotene in the human body: metabolic bioactivation pathways – from digestion to tissue distribution and excretion
β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive carotenoid-metabolites can modulate the expression of specific genes mainly via the nuclear hormone receptors: retinoic acid receptor- and retinoid X receptor-...
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Published in | Proceedings of the Nutrition Society Vol. 78; no. 1; pp. 68 - 87 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge, UK
Cambridge University Press
01.02.2019
Cambridge University Press (CUP) |
Subjects | |
Online Access | Get full text |
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Abstract | β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive carotenoid-metabolites can modulate the expression of specific genes mainly via the nuclear hormone receptors: retinoic acid receptor- and retinoid X receptor-mediated signalling. To better understand the metabolic conversion of β-carotene, inter-individual differences regarding β-carotene bioavailability and bioactivity are key steps that determine its further metabolism and bioactivation and mediated signalling. Major carotenoid metabolites, the retinoids, can be stored as esters or further oxidised and excreted via phase 2 metabolism pathways. In this review, we aim to highlight the major critical control points that determine the fate of β-carotene in the human body, with a special emphasis on β-carotene oxygenase 1. The hypothesis that higher dietary β-carotene intake and serum level results in higher β-carotene-mediated signalling is partly questioned. Alternative autoregulatory mechanisms in β-carotene / retinoid-mediated signalling are highlighted to better predict and optimise nutritional strategies involving β-carotene-related health beneficial mediated effects. |
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AbstractList | β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive carotenoid-metabolites can modulate the expression of specific genes mainly via the nuclear hormone receptors: retinoic acid receptor- and retinoid X receptor-mediated signalling. To better understand the metabolic conversion of β-carotene, inter-individual differences regarding β-carotene bioavailability and bioactivity are key steps that determine its further metabolism and bioactivation and mediated signalling. Major carotenoid metabolites, the retinoids, can be stored as esters or further oxidised and excreted via phase 2 metabolism pathways. In this review, we aim to highlight the major critical control points that determine the fate of β-carotene in the human body, with a special emphasis on β-carotene oxygenase 1. The hypothesis that higher dietary β-carotene intake and serum level results in higher β-carotene-mediated signalling is partly questioned. Alternative autoregulatory mechanisms in β-carotene / retinoid-mediated signalling are highlighted to better predict and optimise nutritional strategies involving β-carotene-related health beneficial mediated effects. β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive carotenoid-metabolites can modulate the expression of specific genes mainly via the nuclear hormone receptors: retinoic acid receptor- and retinoid X receptor-mediated signalling. To better understand the metabolic conversion of β-carotene, inter-individual differences regarding β-carotene bioavailability and bioactivity are key steps that determine its further metabolism and bioactivation and mediated signalling. Major carotenoid metabolites, the retinoids, can be stored as esters or further oxidised and excreted via phase 2 metabolism pathways. In this review, we aim to highlight the major critical control points that determine the fate of β-carotene in the human body, with a special emphasis on β-carotene oxygenase 1. The hypothesis that higher dietary β-carotene intake and serum level results in higher β-carotene-mediated signalling is partly questioned. Alternative autoregulatory mechanisms in β-carotene / retinoid-mediated signalling are highlighted to better predict and optimise nutritional strategies involving β-carotene-related health beneficial mediated effects.β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive carotenoid-metabolites can modulate the expression of specific genes mainly via the nuclear hormone receptors: retinoic acid receptor- and retinoid X receptor-mediated signalling. To better understand the metabolic conversion of β-carotene, inter-individual differences regarding β-carotene bioavailability and bioactivity are key steps that determine its further metabolism and bioactivation and mediated signalling. Major carotenoid metabolites, the retinoids, can be stored as esters or further oxidised and excreted via phase 2 metabolism pathways. In this review, we aim to highlight the major critical control points that determine the fate of β-carotene in the human body, with a special emphasis on β-carotene oxygenase 1. The hypothesis that higher dietary β-carotene intake and serum level results in higher β-carotene-mediated signalling is partly questioned. Alternative autoregulatory mechanisms in β-carotene / retinoid-mediated signalling are highlighted to better predict and optimise nutritional strategies involving β-carotene-related health beneficial mediated effects. β-Carotene intake and tissue/blood concentrations have been associated with reduced inci-dence of several chronic diseases. Further bioactive carotenoid-metabolites can modulatethe expression of specific genes mainly via the nuclear hormone receptors: retinoic acidreceptor- and retinoid X receptor-mediated signalling. To better understand the metabolicconversion of β-carotene, inter-individual differences regarding β-carotene bioavailabilityand bioactivity are key steps that determine its further metabolism and bioactivation andmediated signalling. Major carotenoid metabolites, the retinoids, can be stored as estersor further oxidised and excreted via phase 2 metabolism pathways. In this review, we aimto highlight the major critical control points that determine the fate of β-carotene in thehuman body, with a special emphasis on β-carotene oxygenase 1. The hypothesis that higherdietary β-carotene intake and serum level results in higher β-carotene-mediated signalling ispartly questioned. Alternative autoregulatory mechanisms in β-carotene / retinoid-mediatedsignalling are highlighted to better predict and optimise nutritional strategies involving β-carotene-related health beneficial mediated effects. |
Author | Keijer, Jaap Desmarchelier, Charles Rühl, Ralph van Schothorst, Evert Bohn, Torsten El, Sedef N. Borel, Patrick |
Author_xml | – sequence: 1 givenname: Torsten surname: Bohn fullname: Bohn, Torsten organization: 1Luxembourg Institute of Health, rue 1 A-B Thomas Edison, L-1445 Strassen, Luxembourg – sequence: 2 givenname: Charles surname: Desmarchelier fullname: Desmarchelier, Charles organization: 2C2VN, Aix-Marseille Univ., INRA, INSERM, Marseille, France – sequence: 3 givenname: Sedef N. surname: El fullname: El, Sedef N. organization: 3Engineering Faculty, Food Engineering Department, Ege University, Izmir, Turkey – sequence: 4 givenname: Jaap surname: Keijer fullname: Keijer, Jaap organization: 4Human and Animal Physiology, Wageningen University, Wageningen, The Netherlands – sequence: 5 givenname: Evert surname: van Schothorst fullname: van Schothorst, Evert organization: 4Human and Animal Physiology, Wageningen University, Wageningen, The Netherlands – sequence: 6 givenname: Ralph surname: Rühl fullname: Rühl, Ralph email: ralphruehl@web.de organization: 5Paprika Bioanalytics BT, Debrecen, Hungary – sequence: 7 givenname: Patrick orcidid: 0000-0001-9977-3238 surname: Borel fullname: Borel, Patrick organization: 2C2VN, Aix-Marseille Univ., INRA, INSERM, Marseille, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30747092$$D View this record in MEDLINE/PubMed https://amu.hal.science/hal-02487119$$DView record in HAL |
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DocumentTitleAlternate | T. Bohn et al. β-Carotene bioactivation pathway |
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Issue | 1 |
Keywords | Vitamin A Nuclear hormone receptor Absorption SNPs Apo-carotenoids Micellisation Retinoic acid |
Language | English |
License | https://www.cambridge.org/core/terms Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0 |
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PublicationDate | 20190200 2019-02-00 20190201 2019-02 |
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PublicationTitle | Proceedings of the Nutrition Society |
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PublicationYear | 2019 |
Publisher | Cambridge University Press Cambridge University Press (CUP) |
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Snippet | β-Carotene intake and tissue/blood concentrations have been associated with reduced incidence of several chronic diseases. Further bioactive... β-Carotene intake and tissue/blood concentrations have been associated with reduced inci-dence of several chronic diseases. Further bioactive... |
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SubjectTerms | beta Carotene - metabolism beta-carotene bioactive properties Bioavailability Biological activity Biological Availability blood serum Carotene Carotenoids chronic diseases Conference on ‘Nutrient–nutrient interaction’ critical control points Diabetes Digestion - physiology Enzymes Esters Excretion Fatty acids Food Food and Nutrition Gene expression genes hormone receptors Human body Human subjects Humans Life Sciences Ligands Lipids Metabolic Networks and Pathways - physiology Metabolism Metabolites Nuclear receptors Nutrition Society Scottish Section Meeting 2018 Oxygenase Particle size Physiology Receptors Retinoic acid retinoic acid receptors Retinoids Signal transduction Signaling Studies Symposium 2: Nutrient interactions and their role in protection from chronic diseases tissue distribution Tissue Distribution - physiology Vitamin A β-Carotene |
Title | β-Carotene in the human body: metabolic bioactivation pathways – from digestion to tissue distribution and excretion |
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