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Vol. 14, No. 2, 2007
Issue release date: Published online first (Issue-in-Progress)
Forsch Komplementärmed 2007;14:70-80
Original Article · Originalarbeit

An Updated Systematic Review of the Pharmacology of Silymarin

Saller R.a · Melzer J.a · Reichling J.b · Brignoli R.c · Meier R.d
aInstitute of Complementary Medicine, Department of Internal Medicine, University Hospital Zurich, Switzerland bInstitute of Pharmacy and Molecular Biotechnology, Department of Biology, Ruprecht-Karls-University Heidelberg, Germany cClinical pharmacology – Tradyser GmbH, Rueschlikon ZH, dDepartment of Gastroenterology, University of Basel, Liestal, Switzerland


Recent years have seen an explosion of scientific papers that deal with drugs from the fruits of milk thistle and its active substances silymarin (standardized mixture of flavonolignanes), thus justifying an updated systematic review. Methods: Electronic databases identified silymarin, silibinin, silicristin or milk thistle as descriptors in >700 papers (34% published in last 5 years; 92% dealt with animal pharmacological). Only papers adequately reporting on experimental conditions, dosing, variables tested and statistics were analysed. Results: Silymarin was found to modify specifically the functions related to various transporters and receptors located in the cell membranes; that is, organic anion uptake transporter peptides (OATP), ABC transporters (P-gp), bile salt export pump, as well as TNF-a-dependent and possibly selectin-dependent phenomena. In the cytoplasm, some antioxidant properties and the inhibition of the lipoxygenase pathway seem quite selective and could concur to the antitoxic effects. Some effects like the inhibition of inducible nitric-oxide synthase, of nuclear factor κ B, and reduction of collagen synthesis are indicative of DNA/RNAmediated effects. Several studies using ‘in vitro’ and ‘in vivo’ cancer models suggest a potential of silymarin in such diseases. Topical and systemic silymarin has skin protective properties against UV-induced damage in epidermis and causes an up-regulation of tumour-suppressor genes p53- and p21CIP1. There were no data on hepatic viral replication, viremia or spontaneous tumours in the data examined. Conclusions: Data presented here do not solve the question about the complex mechanism(s) of action of the medicinal herbal drug silymarin. Silymarin may be a natural multi-functional and multi-target drug.

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