Authors: Prachayasittikul, Virapong
Wanwimolruk, Sompon
Title: Variable inhibitory effect of herbal supplements of different brands on human P450 CYP1A2
Language (ISO): en
Abstract: Herbal supplements are not governed by the same regulations as prescription drugs, we hy-pothesize that the content of their active ingredients may vary largely among different manu-facturers. This may produce variable therapeutic outcomes. This study aims to examine this hypothesis on commonly used herbal supplements among cancer patients. CYP1A2 has been implicated in the activation of many carcinogens and alteration in its activity may be a mech-anism associated with the protective effect of herbal products. Activity of human CYP1A2 was used to determine the effect of four herbal supplements of different brands, namely, black cohosh (BC), ginseng, grape seed extract (GSE) and green tea extract (GTE). The herbal con-tent was extracted with methanol, and extract aliquots were used to determine their effect on CYP1A2. Human liver microsomes, the CYP1A2 probe (7-ethoxyresorufin) and NADPH in buffer were incubated with and without herbal extract. Metabolite (resorufin) formation was monitored by HPLC. Seven BC products caused a mild inhibition of CYP1A2, ranging from 2.4 % by GNC Plus to 21.9 % by Nature’s Resource. Among nine ginseng products tested, the inhibitory effect varied from 4.2 % by Imperial to 44.6 % by Solarays. The effect of nine GSE brands also varied, ranging from 1.7 % (Country Life) to 26.5 % (Veg Life). Of twelve GTE products, the inhibitory effect varied from 2.9 % by Henry’s to 46.6 % by GNC Plus. It ap-pears that the inhibition of selected herbal supplements on CYP1A2 activity varies considera-bly among different brands of the products. This may be due to variations in the herbal prod-ucts’ active ingredients content.
Subject Headings: black cohosh
CYP1A2
dietary supplements
drug interaction
ginseng
grape seed extract
green tea extract
URI: http://hdl.handle.net/2003/29621
http://dx.doi.org/10.17877/DE290R-4920
Issue Date: 2012-09-19
Appears in Collections:Original Articles

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