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Int. J. Mol. Sci. 2011, 12(9), 5592-5603; doi:10.3390/ijms12095592

Epigallocatechin-3-gallate (EGCG) for Clinical Trials: More Pitfalls than Promises?

1
Department of Cardiology, Angiology and Pneumology, University of Heidelberg, D-69120 Heidelberg, Germany
2
Faculty of Medicine, University of Heidelberg, D-69120, Heidelberg, Germany
*
Author to whom correspondence should be addressed.
Received: 14 July 2011 / Revised: 17 August 2011 / Accepted: 19 August 2011 / Published: 31 August 2011
(This article belongs to the Section Biochemistry, Molecular Biology and Biophysics)
View Full-Text   |   Download PDF [321 KB, uploaded 19 June 2014]   |  

Abstract

Epigallocatechin-3-gallate (EGCG), the main and most significant polyphenol in green tea, has shown numerous health promoting effects acting through different pathways, as antioxidant, anti-inflammatory and anti-atherogenic agent, showing gene expression activity, functioning through growth factor-mediated pathways, the mitogen-activated protein kinase-dependent pathway, the ubiquitin/proteasome degradation pathway, as well as eliciting an amyloid protein remodeling activity. However, epidemiological inferences are sometimes conflicting and in vitro and in vivo studies may seem discrepant. Current knowledge on how to enhance bioavailability could be the answer to some of these issues. Furthermore, dose levels, administration frequency and potential side effects remain to be examined. View Full-Text
Keywords: epigallocatechin-3-gallate; green tea; bioavailability epigallocatechin-3-gallate; green tea; bioavailability
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This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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Mereles, D.; Hunstein, W. Epigallocatechin-3-gallate (EGCG) for Clinical Trials: More Pitfalls than Promises? Int. J. Mol. Sci. 2011, 12, 5592-5603.

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