Literature DB >> 24158698

EGCG inhibit chemical reactivity of iron through forming an Ngal-EGCG-iron complex.

Guan-Hu Bao1, Jie Xu, Feng-Lin Hu, Xiao-Chun Wan, Shi-Xian Deng, Jonathan Barasch.   

Abstract

Accumulated evidence indicates that the interconversion of iron between ferric (Fe(3+)) and ferrous (Fe(2+)) can be realized through interaction with reactive oxygen species in the Fenton and Haber-Weiss reactions and thereby physiologically effects redox cycling. The imbalance of iron and ROS may eventually cause tissue damage such as renal proximal tubule injury and necrosis. Many approaches were exploited to ameliorate the oxidative stress caused by the imbalance. (-)-Epigallocatechin-3-gallate, the most active and most abundant catechin in tea, was found to be involved in the protection of a spectrum of renal injuries caused by oxidative stress. Most of studies suggested that EGCG works as an antioxidant. In this paper, Multivariate analysis of the LC-MS data of tea extracts and binding assays showed that the tea polyphenol EGCG can form stable complex with iron through the protein Ngal, a biomarker of acute kidney injury. UV-Vis and Luminescence spectrum methods showed that Ngal can inhibit the chemical reactivity of iron and EGCG through forming an Ngal-EGCG-iron complex. In thinking of the interaction of iron and ROS, we proposed that EGCG may work as both antioxidant and Ngal binding siderphore in protection of kidney from injuries.

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Year:  2013        PMID: 24158698      PMCID: PMC4416964          DOI: 10.1007/s10534-013-9681-8

Source DB:  PubMed          Journal:  Biometals        ISSN: 0966-0844            Impact factor:   2.949


  39 in total

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  12 in total

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Authors:  Rattiyaporn Kanlaya; Visith Thongboonkerd
Journal:  Adv Nutr       Date:  2019-01-01       Impact factor: 8.701

3.  The Ligands of Neutrophil Gelatinase-Associated Lipocalin.

Authors:  Guan-Hu Bao; Chi-Tang Ho; Jonathan Barasch
Journal:  RSC Adv       Date:  2015-12-03       Impact factor: 3.361

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Journal:  Biometals       Date:  2016-03-23       Impact factor: 2.949

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Journal:  Cell Mol Gastroenterol Hepatol       Date:  2016-07
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