食品科学 ›› 2012, Vol. 33 ›› Issue (3): 215-219.doi: 10.7506/spkx1002-6630-201203045

• 营养卫生 • 上一篇    下一篇

鹰嘴豆肽抑制肿瘤作用和对免疫功能的影响

高 捷,王 华,寇晓虹,薛照辉   

  1. 天津大学化工学院食品科学系
  • 出版日期:2012-02-15 发布日期:2012-02-14
  • 基金资助:
    天津大学创新基金项目(2010XJ-0216)

Antitumor and Immune-Enhancing Activity of Chickpea Peptides in Hepatoma H22-Bearing Mice

GAO Jie,WANG Hua,KOU Xiao-hong,XUE Zhao-hui   

  1. Department of Food Science, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China
  • Online:2012-02-15 Published:2012-02-14

摘要: 目的:探讨鹰嘴豆肽抑制肝癌H22细胞移植瘤的效果及对免疫功能的影响。方法:将小鼠随机分为正常对照组、阳性对照组、肿瘤对照组和鹰嘴豆肽低、中、高剂量组(50、100、200mg/(kg·d)),除正常组外,其余各组小鼠均在皮下接种肝癌H22细胞,建立肝癌小鼠模型。建模后第2天开始灌胃给药,连续给药10d。末次给药24h后拉托颈椎处死小鼠,测体质量、肿瘤大小、抑瘤率、胸腺指数、脾指数、巨噬细胞吞噬能力、脾细胞吞噬能力等。 结果:鹰嘴豆肽低、中、高3个剂量均可抑制H22肿瘤的生长,且没有阻碍小鼠体质量和免疫器官的增长。与肿瘤对照组相比,鹰嘴豆高剂量组可以显著提高小鼠迟发型超敏反应(DTH)的能力、淋巴细胞和巨噬细胞吞噬能力(P<0.05),鹰嘴豆低、中剂量组对其也有一定的改善作用,但是没有表现出剂量依赖效应。 讨论:鹰嘴豆肽可能是通过增强H22肝癌小鼠的免疫功能来抑制肿瘤的生长,具体的作用机制还需要更深入的研究。

关键词: 鹰嘴豆肽, 抗肿瘤, H22肿瘤, 免疫功能

Abstract: Objective: To find out whether chickpea peptides has antitumor and immune-enhancing activity in hepatoma H22-bearing mice. Methods: KM mice were randomly divided to normal control group, positive control group (PC), tumor control group and chickpea peptide groups at the doses of 50, 100 mg/(kg·d) and 200 mg/(kg·d). The H22-bearing mice were treated with chickpea peptide and Cy by gavage at the volume of 0.2 mL/mouse per day for 10 consecutive days. Distilled water was used for the normal control group. The body weight, tumor growth, tumor inhibitory rate, thymus index, spleen index, cell-mediated immune functions including lymphocyte proliferation, peritoneal macrophage phagocytosis and splenic lymphocytes were detected at 24 h after the last administration. Results: An inhibitory tend of tumor growth was observed in the chickpea peptide group. Compared with the tumor control group, a significant increase in relative spleen weight, delayed-type hypersensitivity (DTH), peritoneal macrophage phagocytotic activity and splenic lymphocyte in the chickpea groups was also observed. However, no dose-dependent effect was achieved. Conclusion: Peptides derived from chickpea have anti-tumor activity probably by enhancing immune functions in hepatoma H22-bearing mice. The detailed mechanism remains to be further studied.

Key words: chickpea, anti-tumor, hepatoma-H22, immune function

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