Green-tea polyphenol (-)-epigallocatechin-3-gallate provides resistance to apoptosis in isolated islets

被引:24
作者
Hara, Yuko
Fujino, Masayuki [1 ]
Takeuchi, Masao
Li, Xiao-Kang
机构
[1] Natl Res Inst Child Hlth & Dev, Lab Transplantat Immunol, Tokyo, Japan
[2] Natl Inst Infect Dis, AIDS Res Ctr, Tokyo 2080011, Japan
[3] Nikken Seil Corp, Japan Inst Control Aging, Shizuoka, Japan
来源
JOURNAL OF HEPATO-BILIARY-PANCREATIC SURGERY | 2007年 / 14卷 / 05期
关键词
(-)-epigallocatechin-3-gallate; islet; apoptosis; anoikis; hypoxia; reoxygenation;
D O I
10.1007/s00534-006-1207-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Purpose: Apoptosis resulting from disruption of the normal cell-matrix relationship (anoikis) during islet isolation, and the reactive oxygen and nitrogen species generated following hypoxia/reoxygenation (H/R) can lead to a loss of islet tissue in culture and the reduced survival of transplanted pancreatic islets. The aim of this study was to investigate the effect of (-)-epigallocatechin-3-gallate (EGCG), a well-known antiapoptotic agent, on inhibiting anoikis and H/R injury in an in vitro islet culture system. Methods: Islets were isolated from F344 rats and cultured under normal or H/R condition with/without EGCG. Results:GCG inhibited apoptosis and lactate-dehydrogenase leakage from anoikis and H/R in a dose-dependent manner. Further, EGCG prevent increases in 8-hydroxy-2'-deoxyguanosine content and inhibited the decline of insulin secretory function induced by H/R. Conclusions: suggest that the addition of EGCG to an islet culture system may improve the survival rate of isolated islets and reduce the loss of functional islet mass that compromises the stable reversal of diabetes after islet transplantation.
引用
收藏
页码:493 / 497
页数:5
相关论文
共 11 条
[1]   Inhibition of caspase-mediated PARP-1 cleavage results in increased necrosis in isolated islets of Langerhans [J].
Aikin, R ;
Rosenberg, L ;
Paraskevas, S ;
Maysinger, D .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2004, 82 (06) :389-397
[2]   Detection of oxidative DNA damage to ischemic reperfused rat hearts by 8-hydroxydeoxyguanosine formation [J].
Cordis, GA ;
Maulik, G ;
Bagchi, D ;
Riedel, W ;
Das, DK .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (10) :1939-1944
[3]   Adenovirus-mediated hepatocyte growth factor expression in mouse islets improves pancreatic islet transplant performance and reduces beta cell death [J].
García-Ocaña, A ;
Takane, KK ;
Reddy, VT ;
Lopez-Talavera, JC ;
Vasavada, RC ;
Stewart, AF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (01) :343-351
[4]   AN IMPROVED METHOD FOR ISOLATION OF MOUSE PANCREATIC-ISLETS [J].
GOTOH, M ;
MAKI, T ;
KIYOIZUMI, T ;
SATOMI, S ;
MONACO, AP .
TRANSPLANTATION, 1985, 40 (04) :437-438
[5]   Pancreatic islet cell transplantation using non-heart-beating donors (NHBDs) [J].
Matsumoto, S ;
Tanaka, K .
JOURNAL OF HEPATO-BILIARY-PANCREATIC SURGERY, 2005, 12 (03) :227-230
[6]   Caspase-3 inhibitor prevents apoptosis of human islets immediately after isolation and improves islet graft function [J].
Nakano, M ;
Matsumoto, I ;
Sawada, T ;
Ansite, J ;
Oberbroeckling, J ;
Zhang, HJ ;
Kirchhof, N ;
Shearer, J ;
Sutherland, DER ;
Hering, BJ .
PANCREAS, 2004, 29 (02) :104-109
[7]   Protection against lipoapoptosis of β cells through leptin-dependent maintenance of Bcl-2 expression [J].
Shimabukuro, M ;
Wang, MY ;
Zhou, YT ;
Newgard, CB ;
Unger, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9558-9561
[8]   Mechanisms of action of green tea catechins, with a focus on ischemia-induced neurodegeneration [J].
Sutherland, Brad A. ;
Rahman, Rosanna M. A. ;
Appleton, Ian .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2006, 17 (05) :291-306
[9]   A tripartite anoikis-like mechanism causes early isolated islet apoptosis [J].
Thomas, F ;
Wu, JG ;
Contreras, JL ;
Smyth, C ;
Bilbao, G ;
He, J ;
Thomas, J .
SURGERY, 2001, 130 (02) :333-338
[10]   Regenerative medicine of the pancreatic β cells [J].
Yamada, S ;
Kojima, I .
JOURNAL OF HEPATO-BILIARY-PANCREATIC SURGERY, 2005, 12 (03) :218-226