Article ID Journal Published Year Pages File Type
1930859 Biochemical and Biophysical Research Communications 2011 5 Pages PDF
Abstract

Tea is widely consumed all over the world. Studies have demonstrated the role of tea in prevention and treatment of various chronic diseases including diabetes and obesity, but the underlying mechanism is unclear. PTP1B is a widely expressed tyrosine phosphatase which has been defined as a target for therapeutic drug development to treat diabetes and obesity. In screening for inhibitors of PTP1B, we found that aqueous extracts of teas exhibited potent PTP1B inhibitory effects with an IC50 value of 0.4–4 g dry tea leaves per liter of water. Black tea shows the strongest inhibition activities, followed by oolong and then by green tea. Biochemical fractionations demonstrated that the major effective components in tea corresponded to oxidized polyphenolic compounds. This was further verified by the fact that tea catechins became potent inhibitors of PTP1B upon oxidation catalyzed by tyrosinases. When applied to cultured cells, tea extracts induced tyrosine phosphorylation of cellular proteins. Our study suggests that some beneficial effects of tea may be attributed to the inhibition of PTP1B.

► Tea extracts inhibits tyrosine phosphatase PTP1B with high potency. ► Black teas are more effective than green teas. ► The effective components are oxidized tea catechins. ► Tea extracts induce tyrosine phosphorylation of proteins in cultured cells.

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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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