Abstract |
Inhibition of protein tyrosine phosphatase 1B (PTP1B) has been proposed as a therapy for treatment of type 2 diabetes and obesity. Bioassay-guided fractionation of the MeOH extract of the leaves and stems of Symplocos paniculata (Thunb.) Miq. (Symplocaceae), using an in vitro PTP1B inhibitory assay, resulted in the isolation of three ursane-type triterpenes, ursolic acid (1), corosolic acid (2) and 2alpha,3alpha,19alpha,23-tetrahydroxyurs-12-en-28-oic acid (3). Compounds 1-3 inhibited PTP1B with IC (50) values of 3.8 +/- 0.5, 7.2 +/- 0.8 and 42.1 +/- 1.5 microM, respectively. Kinetic studies suggest that 1 is a competitive inhibitor with a K(i) value of 2.0 microM, whereas 2 is a mixed-type inhibitor of PTP1B. Our results indicate that the substitution of hydroxy groups on the ursane-type triterpenes is responsible for the loss of activity, and thus 1 and 2 possessing only one or two hydroxy groups can be potential PTP1B inhibitors.
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Authors | Minkyun Na, Seungmi Yang, Long He, Hyuncheol Oh, Beom Seok Kim, Won Keun Oh, Bo Yeon Kim, Jong Seog Ahn |
Journal | Planta medica
(Planta Med)
Vol. 72
Issue 3
Pg. 261-3
(Feb 2006)
ISSN: 0032-0943 [Print] Germany |
PMID | 16534732
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Enzyme Inhibitors
- Hypoglycemic Agents
- Plant Extracts
- Triterpenes
- PTPN1 protein, human
- Protein Tyrosine Phosphatase, Non-Receptor Type 1
- Protein Tyrosine Phosphatases
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Topics |
- Acanthaceae
- Diabetes Mellitus, Type 2
(drug therapy)
- Enzyme Inhibitors
(administration & dosage, pharmacology, therapeutic use)
- Humans
- Hypoglycemic Agents
(administration & dosage, pharmacology, therapeutic use)
- Inhibitory Concentration 50
- Obesity
(drug therapy)
- Phytotherapy
- Plant Extracts
(administration & dosage, pharmacology, therapeutic use)
- Plant Leaves
- Plant Stems
- Protein Tyrosine Phosphatase, Non-Receptor Type 1
- Protein Tyrosine Phosphatases
(drug effects)
- Triterpenes
(administration & dosage, pharmacology, therapeutic use)
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