(-)-表没食子儿茶素没食子酸酯对7,12-二甲基苯[a]蒽诱导的大鼠骨髓细胞染色体畸变的抑制作用

Yoshiaki Ito
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引用次数: 1

摘要

本文研究了绿茶中主要多酚成分(-)-表没食子儿茶素没食子酸酯(EGCG)对7,12-二甲基苯[a]蒽(DMBA)诱导的大鼠骨髓细胞染色体畸变(CA)的抑制作用。在注射DMBA之前给予EGCG的大鼠,其骨髓细胞中DMBA诱导的CA的频率明显受到抑制。在注射DMBA后24、30、48和72 h观察到24 h前给予EGCG (60 mg/kg体重)的抑制作用,但在DMBA治疗后的早期(6、12和18 h)没有观察到EGCG的抑制作用。另一方面,在DMBA注射前0.5 h给予EGCG (60 mg/kg体重),在DMBA注射后的所有时期都能抑制DMBA诱导的CA。所有剂量的DMBA(25、50、75和100 mg/kg)均在24 h或0.5 h前对EGCG有抑制作用。注射DMBA前0.5 h给予60 mg/kg体重的EGCG比24 h给予相同剂量的EGCG有更大的抑制作用。0.5 h前给予EGCG抑制作用在20 ~ 60mg /kg体重范围内呈剂量依赖性。甲基甲磺酸(MMS:直接作用致癌物)诱导的CA不受EGCG的抑制。在注射DMBA前0.5 h给予脱氢表雄酮(DHEA)(一种典型的羟基类固醇硫转移酶底物)也能显著抑制dba诱导的CA,但在注射前24 h给予DHEA则无此作用。这些结果表明,EGCG对dba诱导的CA有两种不同的抑制机制,这取决于给药时间。EGCG对dmba诱导的CA的抑制作用,可能与EGCG对微粒体酶系统的修饰有关,也可能与EGCG对硫转移酶活性的抑制有关。
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Suppressive effect of (-)-epigallocatechin gallate on 7,12-dimethylbenz[a]anthracene-induced chromosome aberrations in rat bone marrow cells
The suppressive effect of (-)-epigallocatechin gallate (EGCG), the major polyphenolic constituent present in green tea, on 7,12-dimethylbenz[a]anthracene (DMBA)-induced chromosome aberrations (CA) in rat bone marrow cells was studied. Rats given EGCG before the DMBA injection displayed a considerably suppressed frequency of DMBA-induced CA in their bone marrow cells. The suppressive effect of EGCG (60 mg/kg body weight) given 24 h before was observed 24, 30, 48 and 72 h after the DMBA injection, but not at the early period (6, 12 and 18 h) after the DMBA treatment. On the other hand, EGCG (60 mg/kg body weight) given 0.5 h before DMBA suppressed DMBA-induced CA at all periods after the DMBA injection. The suppression of EGCG given 24 h or 0.5 h before was observed for all doses of DMBA (25, 50, 75 and 100 mg/kg) investigated. EGCG given at 60 mg/kg body weight 0.5 h before the DMBA injection showed greater suppressive effect than the same dose given 24 h before. The suppressive effect of EGCG given 0.5 h before was dosedependent in the range of 20-60 mg/kg body weight. Methyl methanesulfonate (MMS: direct-acting carcinogen)-induced CA were not suppressed by EGCG.The administration of dehydroepiandrosterone (DHEA), a typical substrate for hydroxysteroid sulfotransferases, 0.5 h before DMBA injection also significantly suppressed DMBA-induced CA but DHEA given 24 h before did not.These results suggest that EGCG has two different suppression mechanisms for DMBA-induced CA depending on the administration time. The suppression of DMBA-induced CA by EGCG given 24 h or 0.5 h before may result from the modification of microsomal enzyme system or the inhibition of sulfotransferase activity by EGCG, respectively.
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