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Wiley InterScience | ||||||||||||||
![]() Aging CellSee Also: Volume 7 Issue 1, Pages 69 - 77 Published Online: 13 Nov 2007 Journal compilation © 2010 Blackwell Publishing Ltd/The Anatomical Society of Great Britain and Ireland Published on behalf of the Anatomical Society of Great Britain and Ireland
Abstract | References | Full Text: HTML, PDF (Size: 468K) | Related Articles | Citation Tracking Black tea polyphenols mimic insulin/insulin-like growth factor-1 signalling to the longevity factor FOXO1a Copyright Journal compilation © Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland 2007 KEYWORDS Akt • diabetes • FOXO1a • insulin • PEPCK • theaflavin ABSTRACTIn vertebrates and invertebrates, relationships between diet and health are controlled by a conserved signalling pathway responsive to insulin-like ligands. In invertebrate models for example, forkhead transcription factor family O (FOXO) transcription factors in this pathway regulate the rate of aging in response to dietary cues, and in vertebrates, obesity and age-induced deficits in the same pathway are thought to contribute to dysregulation of hepatic gluconeogenesis through genes such as phosphoenolpyruvate carboxykinase (PEPCK). Recently, we have begun to screen for dietary constituents capable of regulating this pathway in our cell culture model. Here, we identify three black tea theaflavins, theaflavin 3-O-gallate, theaflavin 3'-O-gallate, theaflavin 3,3'di-O-gallate and thearubigins as novel mimics of insulin/IGF-1 action on mammalian FOXO1a, PEPCK and moreover we provide evidence that the effects on this pathway of the green tea constituent (-)-epigallocatechin gallate depend on its ability to be converted into these larger structures. With the exception of water, tea is the most popular drink globally, but despite this, little is known about the biological availability of black tea polyphenols in vivo or the molecular target(s) mediating the effects presented here. Further investigation in these two areas might provide insight into how age-related metabolic disease may be deferred. Accepted for publication 2 November 2007 |
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