Thearubigin, the major polyphenol of black tea, ameliorates mucosal injury in trinitrobenzene sulfonic acid-induced colitis

被引:60
作者
Maity, S
Ukil, A
Karmakar, S
Datta, N
Chaudhuri, T
Vedasiromoni, JR
Ganguly, DK
Das, PK
机构
[1] Indian Inst Chem Biol, Mol Cell Biol Lab, Kolkata 700032, W Bengal, India
[2] Tea Res Assoc, Kolkata 700016, W Bengal, India
[3] Indian Inst Chem Biol, Dept Drug Dev, Kolkata 700032, W Bengal, India
关键词
theambigin; inflammatory bowel disease; black tea; colitis; cytokine; nitric oxide (NO) synthase; inducible; NF-kappa B (nuclear factor kappa B);
D O I
10.1016/S0014-2999(03)01760-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inflammatory bowel disease is characterized by oxidative and nitrosative stress, leukocyte infiltration and upregulation of proinflammatory cytokines. The aim of the present study was to examine the protective effects of thearubigin, an anti-inflammatory and anti-oxidant beverage derivative, on 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis in mice, a model for inflammatory bowel disease. Intestinal lesions (judged by macroscopic and histological score) were associated with neutrophil infiltration (measured as increase in myeloperoxidase activity in the mucosa), increased serine protease activity (may be involved in the degradation of colonic tissue) and high levels of malondialdehyde (an indicator of lipid peroxidation). Both nitric oxide (NO) and O-2(-) were increased with concomitant upregulation in the mRNA expression of proinflammatory cytokine response and inducible NO synthase (iNOS). Dose-response studies revealed that pretreatment of mice with thearubigin (40 mg kg(-1) day(-1), i.g. for 10 days) significantly ameliorated the appearance of diarrhoea and the disruption of colonic architecture. Higher dose (100 mg kg(-1)) had comparable effects. This was associated with a significant reduction in the degree of both neutrophil infiltration and lipid peroxidation in the inflamed colon as well as decreased serine protease activity. Thearubigin also reduced the levels of NO and O-2(-) associated with the favourable expression of T-helper 1 cytokines and iNOS. Consistent with these observations, nuclear factor kappa B (NF-kappaB) activation in colonic mucosa was suppressed in thearubigin-treated mice. The results of this study suggest that thearubigin, the most predominant polyphenol of black tea, exerts beneficial effects in experimental colitis and may, therefore, be useful in the treatment of inflammatory bowel disease. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 112
页数:10
相关论文
共 48 条
[1]   The chemistry of tea flavonoids [J].
Balentine, DA ;
Wiseman, SA ;
Bouwens, LCM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :693-704
[2]   Inhibition of inducible nitric oxide synthase gene expression and enzyme activity by epigallocatechin gallate, a natural product from green tea [J].
Chan, MMY ;
Fong, D ;
Ho, CT ;
Huang, HI .
BIOCHEMICAL PHARMACOLOGY, 1997, 54 (12) :1281-1286
[3]  
Chen C-W., 1995, J. Food Lipids, V2, P35, DOI [DOI 10.1111/J.1745-4522.1995.TB00028.X, 10.1111/j.1745-4522.1995.tb00028.x]
[4]   The effects of phenolic components of tea on the production of pro- and anti-inflammatory cytokines by human leukocytes in vitro [J].
Crouvezier, S ;
Powell, B ;
Keir, D ;
Yaqoob, P .
CYTOKINE, 2001, 13 (05) :280-286
[5]   Tempol, a membrane-permeable radical scavenger, reduces dinitrobenzene sulfonic acid-induced colitis [J].
Cuzzocrea, S ;
McDonald, MC ;
Mazzon, E ;
Dugo, L ;
Lepore, V ;
Fonti, MT ;
Ciccolo, A ;
Terranova, ML ;
Caputa, AP ;
Thiemermann, C .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 406 (01) :127-137
[6]  
FERETTI M, 1997, DIGEST DIS SCI, V42, P2606
[7]   Anti-interleukin 12 treatment regulates apoptosis of Th1 T cells in experimental colitis in mice [J].
Fuss, IJ ;
Marth, T ;
Neurath, MF ;
Pearlstein, GR ;
Jain, A ;
Strober, W .
GASTROENTEROLOGY, 1999, 117 (05) :1078-1088
[8]   Expression of nitric oxide synthase in ulcerative colitis [J].
Godkin, AJ ;
DeBelder, AJ ;
Villa, L ;
Wong, A ;
Beesley, JE ;
Kane, SP ;
Martin, JF .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1996, 26 (10) :867-872
[9]  
Gunawardana SC, 1997, J AM VET MED ASSOC, V211, P318
[10]   Drug therapy - Inflammatory bowel disease [J].
Hanauer, SB .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (13) :841-848