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Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on September 3, 2003; DOI: 10.1124/jpet.103.054460


0022-3565/03/3071-254-261$20.00
JPET 307:254-261, 2003
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INFLAMMATION AND IMMUNOPHARMACOLOGY

Anti-Inflammatory Actions of St. John's Wort: Inhibition of Human Inducible Nitric-Oxide Synthase Expression by Down-Regulating Signal Transducer and Activator of Transcription-1{alpha} (STAT-1{alpha}) Activation

Elisa Tedeschi, Marta Menegazzi, Daniela Margotto, Hisanori Suzuki, Ulrich Förstermann, and Hartmut Kleinert

Biochemistry Section, Department of Neuroscience and Vision, University of Verona, Verona, Italy (E.T., M.M., D.M., H.S.); Department of Pharmacology, Johannes Gutenberg University, Mainz, Germany (U.F., H.K.)

St. John's wort (SJW) has been described to show anti-inflammatory properties due to its inhibitory effects on the expression of pro-inflammatory genes like cyclooxygenase-2, interleukin-6, and inducible nitric-oxide synthase (iNOS). Since iNOS plays a critical role in chronic inflammatory diseases, we have focused our attention on the regulation of iNOS expression by SJW in two different human epithelial cell lines, alveolar A549/8 and colon DLD-1 cells. SJW extract concentration dependently inhibited human iNOS expression evaluated by measuring the amounts of iNOS mRNA, iNOS protein, and NO production in both cell lines. This inhibitory effect resulted from transcriptional inhibition as shown in reporter gene experiments. With electrophoretic mobility shift experiments, we found a SJW-mediated down-regulation of the DNA binding activity of the transcription factor signal transducer and activator of transcription-1{alpha} (STAT-1{alpha}), but not of nuclear factor-{kappa}B. This down-regulation of the STAT-1{alpha} DNA binding was shown to result from reduced tyrosine phosphorylation of the STAT-1{alpha} protein. The diminished STAT-1{alpha} tyrosine phosphorylation resulted from SJW-mediated reduction of Janus kinase 2 activity. These data suggest that extracts from SJW may be a promising anti-inflammatory principle in chronic inflammatory diseases.


Received May 13, 2003; accepted June 20, 2003.

Address correspondence to: Dr. Hartmut Kleinert, Department of Pharmacology, Johannes Gutenberg University, Obere Zahlbacher Str. 67, 55101 Mainz, Germany. E-mail: Kleinert{at}mail.uni-mainz.de




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