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DOI: 10.1055/s-0031-1298242
© Georg Thieme Verlag KG Stuttgart · New York
Ratanhiaphenol III from Ratanhiae Radix is a PTP1B Inhibitor
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.
Key words
PTP1B inhibition - Ratanhiae radix - Krameria lappacea - Krameriaceae - ratanhiaphenol III
References
- 1 Unwin N, Whiting D, Gan D, Jacqmain O, Ghyoot G. IDF diabetes atlas. Brussels: International Diabetes Federation; 2009
- 2 Moller D E. New drug targets for type 2 diabetes and the metabolic syndrome. Nature. 2001; 414 821-827
- 3 Zhang Z Y, Lee S Y. PTP1B inhibitors as potential therapeutics in the treatment of type 2 diabetes and obesity. Exp Opin Invest Drugs. 2003; 12 223-233
- 4 Bandyopadhyay D, Kusari A, Kenner K A, Liu F, Chernoff J, Gustafson T A, Kusari J. PTP1B complexes with the insulin receptor in vivo and is tyrosine-phosphorylated in the presence of insulin. J Biol Chem. 1997; 272 1639-1645
- 5 Koren S, Fantus I G. Inhibition of the protein tyrosine phosphatase 1B: potential therapy for obesity, insulin resistance and type II diabetes mellitus. Best Pract Res Clin Endocrinol Metab. 2007; 21 621-640
- 6 Elchebly M, Payette P, Michaliszyn E, Cromlish W, Collins S, Loy A L, Normandin D, Cheng A, Himms-Hagen J, Chan C C, Ramachandran C, Gresser M J, Tremblay M L, Kennedy B. Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase 1B gene. Science. 1999; 283 1544-1548
- 7 Baumgartner L, Sosa S, Atanasov A G, Bodensieck A, Fakhrudin N, Bauer J, Del Favero G, Ponti C, Heiss E H, Schwaiger S, Ladurner A, Widowitz U, Della Loggia R, Rollinger J M, Werz O, Bauer R, Dirsch V M, Tubaro A, Stuppner H. Lignan derivatives from Krameria lappacea roots inhibit acute inflammation in vivo and proinflammatory mediators in vitro. J Nat Prod. 2011; 74 1779-1786
- 8 Dixit M, Saeed U, Kumar A, Siddigi M, Tamrakar A K, Srivastava A K, Goel A. Synthesis, molecular docking and PTP1B inhibitory activity of functionalized 4,5-dihydronaphtofurans and dibenzofurans. Med Chem. 2010; 20 3329-3337
- 9 Zhang W, Hong D, Zhou Y, Zhang Y, Shen Q, Li J Y, Hu L H, Li J. Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and glucose uptake. Biochim Biophys Acta. 2006; 1760 1505-1512
- 10 Baumgartner R R, Steinmann D, Heiss E H, Atanasov A G, Ganzera M, Stuppner H, Dirsch V M. Bioactivity-guided isolation of 1,2,3,4,6-penta-O-galloyl-D-glucopyranose from Paeonia lactiflora as PTP1B inhibitor. J Nat Prod. 2010; 73 1578-1581
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