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

被引:35
作者
Bao, Guan-Hu [1 ]
Xu, Jie [1 ]
Hu, Feng-Lin [2 ]
Wan, Xiao-Chun [1 ]
Deng, Shi-Xian [3 ]
Barasch, Jonathan [3 ]
机构
[1] Anhui Agr Univ, Key Lab Tea Biochem & Biotechnol, Hefei 230036, Anhui, Peoples R China
[2] Anhui Agr Univ, Res Ctr Entomogenous Fungi, Hefei 230036, Anhui, Peoples R China
[3] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
基金
美国国家科学基金会;
关键词
EGCG; Ngal; Siderophore; Antioxidant; Renal injury; GREEN TEA POLYPHENOL; GELATINASE-ASSOCIATED LIPOCALIN; OXIDATIVE STRESS; RENAL INJURY; KIDNEY; REPERFUSION; PROTECTION; EXTRACT; RATS;
D O I
10.1007/s10534-013-9681-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulated evidence indicates that the interconversion of iron between ferric (Fe3+) and ferrous (Fe2+) 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.
引用
收藏
页码:1041 / 1050
页数:10
相关论文
共 40 条
[1]  
Abdel-Raheem IT, 2010, PAK J PHARM SCI, V23, P21
[2]   The chemistry of tea flavonoids [J].
Balentine, DA ;
Wiseman, SA ;
Bouwens, LCM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :693-704
[3]  
Bao GH, 2010, NAT CHEM BIOL, V6, P602, DOI [10.1038/nchembio.402, 10.1038/NCHEMBIO.402]
[4]   Reduction of circulating redox-active iron by apotransferrin protects against renal ischemia-reperfusion injury [J].
De Vries, B ;
Walter, SJ ;
Von Bonsdorff, L ;
Wolfs, TGAM ;
Van Heurn, LWE ;
Parkkinen, J ;
Buurman, WA .
TRANSPLANTATION, 2004, 77 (05) :669-675
[5]   Novel chemotherapeutic and renal protective effects for the green tea (EGCG): Role of oxidative stress and inflammatory-cytokine signaling [J].
El-Mowafy, A. M. ;
Al-Gayyar, M. M. ;
Salem, H. A. ;
El-Mesery, M. E. ;
Darweish, M. M. .
PHYTOMEDICINE, 2010, 17 (14) :1067-1075
[6]   MAJOR ROLE OF HYDROXYL RADICAL IN THE CONVERSION OF CREATININE TO CREATOL [J].
FUJITSUKA, N ;
YOKOZAWA, T ;
OURA, H ;
NAKAMURA, K ;
IENAGA, K .
NEPHRON, 1994, 68 (02) :280-281
[7]   Secondary metabolite mapping identifies Scutellaria inhibitors of human lung cancer cells [J].
Gao, Jiayu ;
Zhao, Huiying ;
Hylands, Peter J. ;
Corcoran, Olivia .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2010, 53 (03) :723-728
[8]   Protective effect of green tea extract and tea polyphenols against FK506-induced cytotoxicity in renal cells [J].
Hisamura, F ;
Kojima-Yuasa, A ;
Kennedy, DO ;
Matsui-Yuasa, I .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2006, 98 (02) :192-196
[9]   Development of HPLC fingerprints for Mallotus species extracts and evaluation of the peaks responsible for their antioxidant activity [J].
Hoai, N. Nguyen ;
Dejaegher, B. ;
Tistaert, C. ;
Hong, V. Nguyen Thi ;
Riviere, C. ;
Chataigne, G. ;
Van, K. Phan ;
Van, M. Chau ;
Quetin-Leclercq, J. ;
Heyden, Y. Vander .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2009, 50 (05) :753-763
[10]   The Role of Electrostatics in Siderophore Recognition by the Immunoprotein Siderocalin [J].
Hoette, Trisha M. ;
Abergel, Rebecca J. ;
Xu, Jide ;
Strong, Roland K. ;
Raymond, Kenneth N. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (51) :17584-17592