Planta Med 2012; 78(7): 678-681
DOI: 10.1055/s-0031-1298242
Biological and Pharmacological Activity
Letters
© Georg Thieme Verlag KG Stuttgart · New York

Ratanhiaphenol III from Ratanhiae Radix is a PTP1B Inhibitor

Elke H. Heiss1 , Lisa Baumgartner2 , Stefan Schwaiger2 , Raul Jimenez Heredia1 , Atanas G. Atanasov1 , Judith M. Rollinger2 , Hermann Stuppner2 , Verena M. Dirsch1
  • 1Department of Pharmacognosy, University of Vienna, Vienna, Austria
  • 2Institute of Pharmacy/Pharmacognosy, Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innsbruck, Austria
Further Information

Publication History

received November 7, 2011 revised January 16, 2012

accepted January 18, 2012

Publication Date:
03 February 2012 (online)

Abstract

The inhibition of protein tyrosine phosphatase 1B (PTP1B) is considered a valid strategy to combat insulin resistance and type II diabetes. We show here that a dichloromethane extract of Ratanhiae radix (RR_ex) dose-dependently inhibits human recombinant PTP1B in vitro and enhances insulin-stimulated glucose uptake in murine myocytes. By determination of the PTP1B inhibiting potential of 11 recently isolated lignan derivatives from RR_ex, the observed activity of the extract could be partly assigned to ratanhiaphenol III. This compound inhibited PTP1B in vitro with an IC50 of 20.2 µM and dose-dependently increased insulin receptor phosphorylation as well as insulin-stimulated glucose uptake in cultured myotubes. This is the first report to reveal an antidiabetic potential for a constituent of rhatany root, traditionally used against inflammatory disorders, by showing its capability of inhibiting PTP1B.

Supporting Information

References

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Dr. Elke Heiss

Department of Pharmacognosy
University of Vienna

Althanstrasse 14

1090 Vienna

Austria

Phone: +43 14 27 75 59 93

Fax: +43 14 27 75 59 69

Email: elke.heiss@univie.ac.at