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The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation

BACKGROUND: Cranberry products have been implicated in several case reports to enhance the anticoagulant effect of warfarin. The mechanism could involve inhibition of the hepatic CYP2C9-mediated metabolic clearance of warfarin by components in cranberry. Because dietary/natural substances vary subst...

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Autores principales: Ngo, Ngoc, Brantley, Scott J, Carrizosa, Daniel R, Kashuba, Angela DM, Dees, E Claire, Kroll, David J, Oberlies, Nicholas H, Paine, Mary F
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943398/
https://www.ncbi.nlm.nih.gov/pubmed/20865058
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author Ngo, Ngoc
Brantley, Scott J
Carrizosa, Daniel R
Kashuba, Angela DM
Dees, E Claire
Kroll, David J
Oberlies, Nicholas H
Paine, Mary F
author_facet Ngo, Ngoc
Brantley, Scott J
Carrizosa, Daniel R
Kashuba, Angela DM
Dees, E Claire
Kroll, David J
Oberlies, Nicholas H
Paine, Mary F
author_sort Ngo, Ngoc
collection PubMed
description BACKGROUND: Cranberry products have been implicated in several case reports to enhance the anticoagulant effect of warfarin. The mechanism could involve inhibition of the hepatic CYP2C9-mediated metabolic clearance of warfarin by components in cranberry. Because dietary/natural substances vary substantially in bioactive ingredient composition, multiple cranberry products were evaluated in vitro before testing this hypothesis in vivo. METHODS: The inhibitory effects of five types of cranberry juices were compared with those of water on CYP2C9 activity (S-warfarin 7-hydroxylation) in human liver microsomes (HLM). The most potent juice was compared with water on S/R-warfarin pharmacokinetics in 16 healthy participants given a single dose of warfarin 10 mg. RESULTS: Only one juice inhibited S-warfarin 7-hydroxylation in HLM in a concentration-dependent manner (P < 0.05), from 20% to >95% at 0.05% to 0.5% juice (v/v), respectively. However, this juice had no effect on the geometric mean AUC(0–∞) and terminal half-life of S/R-warfarin in human subjects. CONCLUSIONS: A cranberry juice that inhibited warfarin metabolism in HLM had no effect on warfarin clearance in healthy participants. The lack of an in vitro–in vivo concordance likely reflects the fact that the site of warfarin metabolism (liver) is remote from the site of exposure to the inhibitory components in the cranberry juice (intestine).
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spelling pubmed-29433982010-09-21 The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation Ngo, Ngoc Brantley, Scott J Carrizosa, Daniel R Kashuba, Angela DM Dees, E Claire Kroll, David J Oberlies, Nicholas H Paine, Mary F J Exp Pharmacol Original Research BACKGROUND: Cranberry products have been implicated in several case reports to enhance the anticoagulant effect of warfarin. The mechanism could involve inhibition of the hepatic CYP2C9-mediated metabolic clearance of warfarin by components in cranberry. Because dietary/natural substances vary substantially in bioactive ingredient composition, multiple cranberry products were evaluated in vitro before testing this hypothesis in vivo. METHODS: The inhibitory effects of five types of cranberry juices were compared with those of water on CYP2C9 activity (S-warfarin 7-hydroxylation) in human liver microsomes (HLM). The most potent juice was compared with water on S/R-warfarin pharmacokinetics in 16 healthy participants given a single dose of warfarin 10 mg. RESULTS: Only one juice inhibited S-warfarin 7-hydroxylation in HLM in a concentration-dependent manner (P < 0.05), from 20% to >95% at 0.05% to 0.5% juice (v/v), respectively. However, this juice had no effect on the geometric mean AUC(0–∞) and terminal half-life of S/R-warfarin in human subjects. CONCLUSIONS: A cranberry juice that inhibited warfarin metabolism in HLM had no effect on warfarin clearance in healthy participants. The lack of an in vitro–in vivo concordance likely reflects the fact that the site of warfarin metabolism (liver) is remote from the site of exposure to the inhibitory components in the cranberry juice (intestine). Dove Medical Press 2010-07-03 /pmc/articles/PMC2943398/ /pubmed/20865058 Text en © 2010 Ngo et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Ngo, Ngoc
Brantley, Scott J
Carrizosa, Daniel R
Kashuba, Angela DM
Dees, E Claire
Kroll, David J
Oberlies, Nicholas H
Paine, Mary F
The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title_full The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title_fullStr The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title_full_unstemmed The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title_short The warfarin–cranberry juice interaction revisited: A systematic in vitro–in vivo evaluation
title_sort warfarin–cranberry juice interaction revisited: a systematic in vitro–in vivo evaluation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943398/
https://www.ncbi.nlm.nih.gov/pubmed/20865058
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