Plasma response to a single dose of dietary βcryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in adult human subjects: A comparative study

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dc.identifier.uri http://dx.doi.org/10.15488/2697
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/2723
dc.contributor.author Breithaupt, Dietmar E.
dc.contributor.author Weller, Philipp
dc.contributor.author Wolters, Maike
dc.contributor.author Hahn, Andreas
dc.date.accessioned 2018-01-29T14:13:19Z
dc.date.available 2018-01-29T14:13:19Z
dc.date.issued 2003
dc.identifier.citation Breithaupt, D.E.; Weller, P.; Wolters, M.; Hahn, A.: Plasma response to a single dose of dietary βcryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in adult human subjects: A comparative study. In: British Journal of Nutrition 90 (2003), Nr. 4, S. 795-801. DOI: https://doi.org/10.1079/BJN2003962
dc.description.abstract Many orange-coloured fruits contain β-cryptoxanthin in its non-esterified as well as its esterified form. Information concerning the absorption of β-cryptoxanthin, especially with regard to the metabolism of its fatty acid esters, is rather scarce. The present study assessed the plasma concentration reached after consumption of a single dose of native β-cryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in equal total amounts. In a randomized, single-blind crossover study, twelve subjects were served a portion of yoghurt containing esterified or non-esterified β-cryptoxanthin (1.3 mg absolute) together with a balanced breakfast. Between the two intervention days, there was a 2-week depletion period. After a fasting blood sample had been taken, futher samples were taken from the subjects at 3, 6, 9, 12 and 24 h. The concentration of non-esterified β-cryptoxanthin in the whole plasma was determined by HPLC; β-cryptoxanthin identification was confirmed by liquid chromatography-atmospheric pressure chemical ionization-MS analyses. Irrespective of the consumed diet, the plasma β-cryptoxanthin concentrations increased significantly (P=0.05) and peaked after 6-12h. The concentration curves, as well as the areas under the curves, were not distinguishable according to two-sided F and t tests (P=0.05). Standardization of β-cryptoxanthin concentrations to plasma triacylglycerol and cholesterol had no impact on the results. Thus, the present study indicates comparable bioavailability of both non-esterified β-cryptoxanthin and mixtures of β-cryptoxanthin esters. The results support the existence of an effective enzymatic cleavage system accepting various p-cryptoxanthin esters. eng
dc.language.iso eng
dc.publisher Cambridge : Cambridge University Press
dc.relation.ispartofseries British Journal of Nutrition 90 (2003), Nr. 4
dc.rights Es gilt deutsches Urheberrecht. Das Dokument darf zum eigenen Gebrauch kostenfrei genutzt, aber nicht im Internet bereitgestellt oder an Außenstehende weitergegeben werden. Dieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
dc.subject β-Cryptoxanthin eng
dc.subject Carotenoid ester eng
dc.subject Liquid chromatography-atmospheric pressure chemical ionization-mass spectroscopy eng
dc.subject Plasma carotenoid response eng
dc.subject beta cryptoxanthin eng
dc.subject cholesterol eng
dc.subject cryptoxanthin eng
dc.subject ester eng
dc.subject triacylglycerol eng
dc.subject unclassified drug eng
dc.subject yoghurt eng
dc.subject antineoplastic agent eng
dc.subject beta carotene eng
dc.subject cholesterol eng
dc.subject cryptoxanthin eng
dc.subject drug derivative eng
dc.subject triacylglycerol eng
dc.subject xanthophyll eng
dc.subject adult eng
dc.subject area under the curve eng
dc.subject article eng
dc.subject bioavailability eng
dc.subject blood level eng
dc.subject blood sampling eng
dc.subject cholesterol blood level eng
dc.subject clinical article eng
dc.subject clinical trial eng
dc.subject comparative study eng
dc.subject controlled clinical trial eng
dc.subject controlled study eng
dc.subject crossover procedure eng
dc.subject diet restriction eng
dc.subject dietary intake eng
dc.subject esterification eng
dc.subject female eng
dc.subject high performance liquid chromatography eng
dc.subject human eng
dc.subject human experiment eng
dc.subject male eng
dc.subject mass spectrometry eng
dc.subject meal eng
dc.subject normal human eng
dc.subject papaya eng
dc.subject randomized controlled trial eng
dc.subject single blind procedure eng
dc.subject standardization eng
dc.subject triacylglycerol blood level eng
dc.subject blood eng
dc.subject chemistry eng
dc.subject diet supplementation eng
dc.subject intestine absorption eng
dc.subject methodology eng
dc.subject papaya eng
dc.subject Carica eng
dc.subject Carica papaya eng
dc.subject Adult eng
dc.subject Anticarcinogenic Agents eng
dc.subject beta Carotene eng
dc.subject Carica eng
dc.subject Cholesterol eng
dc.subject Chromatography, High Pressure Liquid eng
dc.subject Cross-Over Studies eng
dc.subject Dietary Supplements eng
dc.subject Esters eng
dc.subject Female eng
dc.subject Humans eng
dc.subject Intestinal Absorption eng
dc.subject Male eng
dc.subject Single-Blind Method eng
dc.subject Triglycerides eng
dc.subject Xanthophylls eng
dc.subject Yogurt eng
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title Plasma response to a single dose of dietary βcryptoxanthin esters from papaya (Carica papaya L.) or non-esterified β-cryptoxanthin in adult human subjects: A comparative study
dc.type Article
dc.type Text
dc.relation.issn 0007-1145
dc.relation.doi https://doi.org/10.1079/BJN2003962
dc.bibliographicCitation.issue 4
dc.bibliographicCitation.volume 90
dc.bibliographicCitation.firstPage 795
dc.bibliographicCitation.lastPage 801
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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