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CYP3A4 and CYP2D6 inhibitory activities of Indonesian medicinal plants
Thirty samples of Indonesian medicinal plants were analyzed for their capacity to inhibit in vitro metabolism by human cytochrome P450 3A4 (CYP3A4) and CYP2D6 with a radiometric assay. The MeOH-soluble fractions of 25 samples, prepared from water extracts, demonstrated inhibitory activity more than...
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Published in: | Phytomedicine (Stuttgart) 2006-01, Vol.13 (1), p.67-73 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Thirty samples of Indonesian medicinal plants were analyzed for their capacity to inhibit
in vitro metabolism by human cytochrome P450 3A4 (CYP3A4) and CYP2D6 with a radiometric assay. The MeOH-soluble fractions of 25 samples, prepared from water extracts, demonstrated inhibitory activity more than 50% on the metabolism mediated by CYP3A4, and 21 samples on the metabolism mediated by CYP2D6. Among the MeOH-soluble fractions,
Piper nigrum leaf showed the highest inhibitory activity against CYP3A4 (91.7%), and
Punica granatum against CYP2D6 (98.1%). The water extracts of which MeOH-soluble fraction showed inhibitory activity more than 70% were fractionated with EtOAc. From the EtOAc-soluble fractions,
Curcuma heyneana (67.0%),
Pi. cubeba (75.0%),
Pi. nigrum fruit (84.0%),
Pi. nigrum leaf (85.8%), and
Zingiber aromaticum (75.3%) demonstrated inhibitory activity more than 50% on the metabolism mediated by CYP3A4, but only
Pi. nigrum fruit (72.8%) and
Pi. nigrum leaf (69.1%) showed strong inhibitory activity against CYP2D6. For samples that showed more than 70% inhibition, their IC
50 values were determined. The most potent inhibitory activity against CYP3A4 (IC
50 value of 25
μg/ml) was found for the extract of
Pi. nigrum leaf, while that of
Catharanthus roseus showed the most potent inhibitory effect against CYP2D6 (IC
50 value of 11
μg/ml). These results should indicate once more the possibility of potential medicinal plant–drug interactions. |
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ISSN: | 0944-7113 1618-095X |
DOI: | 10.1016/j.phymed.2004.06.022 |