The effect of a catechin-rich extract of Cocos nucifera on lymphocytes proliferation

被引:39
作者
Kirszberg, C
Esquenazi, D
Alviano, CS
Rumjanek, VM
机构
[1] UFRJ, CCS, ICB, Dept Bioquim Med,Lab Imunol Tumoral, BR-21941590 Rio De Janeiro, Brazil
[2] UFRJ, CCS, Inst Biofis Carlos Chagas Filho, Lab Ultraestrutura Celular Hertha Meyer, Rio De Janeiro, Brazil
[3] UFRJ, CCS, Inst Microbiol Professor Paulo Goes, Lab Superficie Microorganismos, Rio De Janeiro, Brazil
关键词
Cocos nucifera; catechins; lymphocytes and leukaemia cells;
D O I
10.1002/ptr.1297
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Catechins are polyphenols with antioxidant activity. The fruit Cocos nucifera (Palmae) has a fiber husk rich in catechins and the local population of northeast Brazil uses it as a medicine against various diseases. An antibacterial and anti-viral activity has been already observed using this substance. Plant extracts, from other sources, rich in catechins are inhibitory to tumour cells, suppressing their proliferation. The aim of the present work was to verify if catechins isolated from Cocos nucifera were capable of inhibiting cell proliferation. An extract obtained from Cocos nucifera was purified through adsorption chromatography using the resin XAD-2. The purified material was used in cultures of an erythroleukaemia cell line (K562) and on normal human peripheral blood lymphocytes. Cell viability was assessed using MTT. Cellular proliferation was measured by [H-3]-thymidine incorporation and cell cycle analysis in a flow cytometer. A dose-dependent inhibitory effect was observed on tumour cells and on lymphocytes activated by phytohemaglutinin (PHA) or phorbol ester. For PHA this effect was irreversible being already established on the first four hours of culture. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:1054 / 1058
页数:5
相关论文
共 23 条
[1]   Green tea constituent epigallocatechin-3-gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells [J].
Ahmad, N ;
Feyes, DK ;
Nieminen, AL ;
Agarwal, R ;
Mukhtar, H .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (24) :1881-1886
[2]   (-)-epigallocatechin-3-gallate inhibition of ultraviolet B induced AP-1 activity [J].
Barthelman, M ;
Bair, WB ;
Stickland, KK ;
Chen, WX ;
Timmermann, N ;
Valcic, S ;
Dong, ZG ;
Bowden, GT .
CARCINOGENESIS, 1998, 19 (12) :2201-2204
[3]   Green tea epigallocatechin gallate shows a pronounced growth inhibitory effect on cancerous cells but not on their normal counterparts [J].
Chen, ZP ;
Schell, JB ;
Ho, CT ;
Chen, KY .
CANCER LETTERS, 1998, 129 (02) :173-179
[4]   Antimicrobial and antiviral activities of polyphenolics from Cocos nucifera Linn. (Palmae) husk fiber extract [J].
Esquenazi, D ;
Wigg, MD ;
Miranda, MMFS ;
Rodrigues, HM ;
Tostes, JBF ;
Rozental, S ;
da Silva, AJR ;
Alviano, CS .
RESEARCH IN MICROBIOLOGY, 2002, 153 (10) :647-652
[5]   ANTICARCINOGENIC EFFECTS OF (-)-EPIGALLOCATECHIN GALLATE [J].
FUJIKI, H ;
YOSHIZAWA, S ;
HORIUCHI, T ;
SUGANUMA, M ;
YATSUNAMI, J ;
NISHIWAKI, S ;
OKABE, S ;
NISHIWAKIMATSUSHIMA, R ;
OKUDA, T ;
SUGIMURA, T .
PREVENTIVE MEDICINE, 1992, 21 (04) :503-509
[6]   Cancer inhibition by green tea [J].
Fujiki, H ;
Suganuma, M ;
Okabe, S ;
Sueoka, N ;
Komori, A ;
Sueoka, E ;
Kozu, T ;
Tada, Y ;
Suga, K ;
Imai, K ;
Nakachi, K .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 402 (1-2) :307-310
[7]  
HU ZQ, 1992, INT J IMMUNOPHARMACO, V14, P1399
[8]   COMPARATIVE ANTILIPOPEROXIDANT, ANTINECROTIC AND SCAVENGING PROPERTIES OF TERPENES AND BIFLAVONES FROM GINKGO AND SOME FLAVONOIDS [J].
JOYEUX, M ;
LOBSTEIN, A ;
ANTON, R ;
MORTIER, F .
PLANTA MEDICA, 1995, 61 (02) :126-129
[9]   Quantitation of chemopreventive synergism between (-)-epigallocatechin-3-gallate and curcumin in normal, premalignant and malignant human oral epithelial cells [J].
Khafif, A ;
Schantz, SP ;
Chou, TC ;
Edelstein, D ;
Sacks, PG .
CARCINOGENESIS, 1998, 19 (03) :419-424
[10]   Suppression of extracellular signals and cell proliferation by the black tea polyphenol, theaflavin-3,3′-digallate [J].
Liang, YC ;
Chen, YC ;
Lin, YL ;
Lin-Shiau, SY ;
Ho, CT ;
Lin, JK .
CARCINOGENESIS, 1999, 20 (04) :733-736