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表没食子儿茶素没食子酸酯 (EGCG) 和叶酸对 N-甲基-N'-硝基-N-亚硝基胍 (MNNG) 诱导的大鼠胃肠道癌症的化学预防作用。

Chemopreventive effect of epigallocatechin-3-gallate (EGCG) and folic acid on the N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced gastrointestinal cancer in rat model.

机构信息

Department of Gastroenterology, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai Institute of Digestive Disease, Shanghai, China.

出版信息

J Dig Dis. 2011 Jun;12(3):181-7. doi: 10.1111/j.1751-2980.2011.00494.x.

Abstract

OBJECTIVE

To investigate the chemopreventive effect and mechanisms of epigallocatechin-3-gallate (EGCG) and folic acid on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced gastrointestinal cancer in rats, and to investigate and compare the combinatorial effects of EGCG and folic acid on the chemoprevention of gastrointestinal carcinogenesis.

METHODS

A total of 159 healthy male Wistar rats were randomly divided into seven groups to have the MNNG in drink (group M), MNNG in drink and EGCG in the feed (group ME), MNNG in drink and folic acid in the feed (group MF), MNNG in drink and EGCG+folic acid in the feed (group MEF), EGCG in the feed (group E), folic acid in the feed (group F) or normal feed (group C), respectively. At 44 weeks, all the rats were killed and assessed for the presence of gastrointestinal tumor. The occurrence of cancer was evaluated by histology. Ki-67 in cancerous tissues and in situ apoptosis were determined by immunohistochemical staining or terminal deoxyribonucleotide transferase-mediated nick-end labeling (TUNEL) assay, respectively.

RESULTS

The experiment was completed in 157 rats (98.74%). As compared with group M, the tumor incidence of group MEF decreased significantly (P=0.011). Ki-67 expression in cancerous tissues of group ME and MEF also decreased significantly (P=0.038, P=0.009), while apoptosis of group ME, MF and MEF increased significantly (P=0.000, P=0.003, P=0.000).

CONCLUSION

EGCG combined with folic acid has an obvious chemopreventive effect on gastrointestinal carcinogenesis induced by MNNG in rats.

摘要

目的

研究表没食子儿茶素没食子酸酯(EGCG)和叶酸对 N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导的大鼠胃肠道肿瘤的化学预防作用及其机制,并探讨和比较 EGCG 和叶酸联合对胃肠道癌发生的化学预防作用。

方法

将 159 只健康雄性 Wistar 大鼠随机分为 7 组,分别饮用 MNNG(组 M)、MNNG 加饲料 EGCG(组 ME)、MNNG 加饲料叶酸(组 MF)、MNNG 加饲料 EGCG 和叶酸(组 MEF)、饲料 EGCG(组 E)、饲料叶酸(组 F)或正常饲料(组 C)。44 周后,所有大鼠均处死并评估胃肠道肿瘤的发生情况。通过组织学评估癌症的发生情况。通过免疫组织化学染色或末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)测定分别检测癌症组织中的 Ki-67 和原位细胞凋亡。

结果

157 只大鼠(98.74%)完成了实验。与组 M 相比,组 MEF 的肿瘤发生率显著降低(P=0.011)。ME 和 MEF 组癌症组织中的 Ki-67 表达也显著降低(P=0.038,P=0.009),而 ME、MF 和 MEF 组的细胞凋亡明显增加(P=0.000,P=0.003,P=0.000)。

结论

EGCG 联合叶酸对 MNNG 诱导的大鼠胃肠道肿瘤具有明显的化学预防作用。

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