Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities

Abstract Background European mistletoe (Viscum album) products used in cancer therapy are frequently combined with other anti-cancer-drugs. Hence, potential herb-drug interactions have become a major safety concern in mistletoe therapy. Methods Three European mistletoe products (Helixor® A, Helixor®...

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Main Authors: Michael Schink, Oliver Dehus
Format: Article
Language:English
Published: BMC 2017-12-01
Series:BMC Complementary and Alternative Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12906-017-2028-1
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spelling doaj-19ea85cdf5df4e1dabbc40ac9872d86a2020-11-25T02:47:08ZengBMCBMC Complementary and Alternative Medicine1472-68822017-12-011711810.1186/s12906-017-2028-1Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activitiesMichael Schink0Oliver Dehus1Helixor Heilmittel GmbHHelixor Heilmittel GmbHAbstract Background European mistletoe (Viscum album) products used in cancer therapy are frequently combined with other anti-cancer-drugs. Hence, potential herb-drug interactions have become a major safety concern in mistletoe therapy. Methods Three European mistletoe products (Helixor® A, Helixor® M and Helixor® P from mistletoe grown on firs, apple trees and pines, respectively) were tested for inhibition of nine major cytochrome P450 (CYP) isoenzymes in a test system using pooled human liver microsomes and for induction of five CYP isoforms in human hepatocytes cultivated in vitro according to the relevant guideline. Results Major inhibition did not occur in any of the CYP marker reactions. For some CYP isoenzymes, a minor or intermediate inhibition could be observed, but without dose effect relationship. Induction activity (≥ 1.5-fold increase) was not found with any of the three mistletoe products. Conclusion Since no induction capacity was found and major inhibition above 50% did not occur even with the highest concentration used, which is approximately 100,000-fold higher than the clinically relevant dose in plasma, a clinically relevant herb-drug interaction is not expected for Helixor® A, M, and P.http://link.springer.com/article/10.1186/s12906-017-2028-1CancerCytochrome P450Helixor®InteractionMistletoeViscum album
collection DOAJ
language English
format Article
sources DOAJ
author Michael Schink
Oliver Dehus
spellingShingle Michael Schink
Oliver Dehus
Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
BMC Complementary and Alternative Medicine
Cancer
Cytochrome P450
Helixor®
Interaction
Mistletoe
Viscum album
author_facet Michael Schink
Oliver Dehus
author_sort Michael Schink
title Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
title_short Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
title_full Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
title_fullStr Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
title_full_unstemmed Effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome P450 activities
title_sort effects of mistletoe products on pharmacokinetic drug turnover by inhibition and induction of cytochrome p450 activities
publisher BMC
series BMC Complementary and Alternative Medicine
issn 1472-6882
publishDate 2017-12-01
description Abstract Background European mistletoe (Viscum album) products used in cancer therapy are frequently combined with other anti-cancer-drugs. Hence, potential herb-drug interactions have become a major safety concern in mistletoe therapy. Methods Three European mistletoe products (Helixor® A, Helixor® M and Helixor® P from mistletoe grown on firs, apple trees and pines, respectively) were tested for inhibition of nine major cytochrome P450 (CYP) isoenzymes in a test system using pooled human liver microsomes and for induction of five CYP isoforms in human hepatocytes cultivated in vitro according to the relevant guideline. Results Major inhibition did not occur in any of the CYP marker reactions. For some CYP isoenzymes, a minor or intermediate inhibition could be observed, but without dose effect relationship. Induction activity (≥ 1.5-fold increase) was not found with any of the three mistletoe products. Conclusion Since no induction capacity was found and major inhibition above 50% did not occur even with the highest concentration used, which is approximately 100,000-fold higher than the clinically relevant dose in plasma, a clinically relevant herb-drug interaction is not expected for Helixor® A, M, and P.
topic Cancer
Cytochrome P450
Helixor®
Interaction
Mistletoe
Viscum album
url http://link.springer.com/article/10.1186/s12906-017-2028-1
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