4.7 Article

Interaction of silymarin components and their sulfate metabolites with human serum albumin and cytochrome P450 (2C9, 2C19, 2D6, and 3A4) enzymes

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 138, 期 -, 页码 -

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2021.111459

关键词

Silymarin; Sulfate conjugates; Human serum albumin; Cytochrome P450; Pharmacokinetic interaction; Herb-drug interaction

资金

  1. New National Excellence Program of the Ministry for Innovation and Technology from the National Research, Development and Innovation Fund [UNKP-20-3-II]
  2. European Union
  3. Czech Science Foundation [18-00121S]
  4. European Social Fund [EFOP-3.6.1.-16-2016-00004]

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The study investigated the interactions of five silymarin components and their sulfate metabolites with human serum albumin and CYP enzymes. The results showed that each compound tested formed stable complexes with albumin, and certain components/metabolites could inhibit CYP enzymes, with 2,3-dehydrosilychristin-19-O-sulfate exhibiting the strongest inhibitory effect on CYP3A4. Hence, caution should be exercised when administering high doses of silymarin concurrently with medications, as interactions may interfere with drug therapy.
Silymarin is a mixture of flavonolignans isolated from the fruit of milk thistle (Silybum marianum (L.) Gaertner). Milk thistle extract is the active ingredient of several medications and dietary supplements to treat liver injury/ diseases. After the oral administration, flavonolignans are extensively biotransformed, resulting in the formation of sulfate and/or glucuronide metabolites. Previous studies demonstrated that silymarin components form stable complexes with serum albumin and can inhibit certain cytochrome P450 (CYP) enzymes. Nevertheless, in most of these investigations, silybin was tested; while no or only limited information is available regarding other silymarin components and metabolites. In this study, the interactions of five silymarin components (silybin A, silybin B, isosilybin A, silychristin, and 2,3-dehydrosilychristin) and their sulfate metabolites were examined with human serum albumin and CYP (2C9, 2C19, 2D6, and 3A4) enzymes. Our results demonstrate that each compound tested forms stable complexes with albumin, and certain silymarin components/metabolites can inhibit CYP enzymes. Most of the sulfate conjugates were less potent inhibitors of CYP enzymes, but 2,3-dehydrosilychristin-19-O-sulfate showed the strongest inhibitory effect on CYP3A4. Based on these observations, the simultaneous administration of high dose silymarin with medications should be carefully considered, because milk thistle flavonolignans and/or their sulfate metabolites may interfere with drug therapy.

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