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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2010
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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). |
format | Text |
id | pubmed-2943398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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