红参对脲脲和苯并(a)芘诱导肺腺瘤小鼠自然杀伤细胞活性的影响。

Y S Yun, H S Moon, Y R Oh, S K Jo, Y J Kim, T K Yun
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引用次数: 0

摘要

先前有报道称红参提取物可抑制脲聚糖、DMBA和黄曲霉毒素B1的致癌作用[Yun等:Cancer Detect prevention 1983;6:515-25]。为了探讨人参的抗癌作用机制,我们在注射尿素脲或苯并(a)芘48周后,观察了自然杀伤细胞(NK)活性和肺腺瘤的发生情况。注射致癌物后4 ~ 24周,NK活性明显降低。这种降低NK活性恢复到对照组水平的管理人参。同时,给小鼠注射尿素后,发现肺腺瘤的发生率较低。然而,苯并(a)芘诱导的肺腺瘤在48周时开始发生,此时NK活性自然下降到低到不受人参影响的水平,人参并没有降低发病率。综上所述,人参的抗癌作用可能与提高NK活性有关。
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Effect of red ginseng on natural killer cell activity in mice with lung adenoma induced by urethan and benzo(a)pyrene.

It was previously reported that red ginseng extract inhibited carcinogenesis by urethan, DMBA, and aflatoxin B1 [Yun et al: Cancer Detect Prevent 1983; 6:515-25]. In an attempt to investigate the mechanism of the anticarcinogenic effect of ginseng, the natural killer (NK) activity and the incidence of lung adenoma were followed over a period of 48 weeks postinjection with urethan or benzo(a)pyrene. The NK activity was markedly depressed from 4 weeks to 24 weeks after injection of carcinogens. This decreased NK activity was returned to the level of controls by administration of ginseng. At the same time, a lower incidence of lung adenoma was noted following administration of ginseng to urethan-injected mice. However, the lung adenoma induced by benzo(a)pyrene began to occur at 48 weeks in which NK activity had naturally declined to a level too low to be affected by ginseng, and administration of ginseng did not decrease the incidence. In conclusion, these results suggest that the anticarcinogenic effect of ginseng may be related to the augmentation of NK activity.

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