苦杏仁苷MF (NSC-15780)单用及联合β -葡萄糖苷酶(NSC-128056)抗肿瘤活性的实验研究。

Cancer chemotherapy reports Pub Date : 1975-09-01
W R Laster, F M Schabel
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引用次数: 0

摘要

我们评估了苦杏仁苷MF单独和与活化剂-葡萄糖苷酶联合对三种可移植的啮齿动物肿瘤的作用;李奇韦骨肉瘤,刘易斯肺癌,和P388白血病。在正常小鼠LD20的剂量反应研究中,单独苦杏仁苷MF对这三种肿瘤系统中的任何一种都没有显着的抗肿瘤活性。同样,在正常小鼠中,当剂量不超过LD10时,苦杏仁苷MF加β -葡萄糖苷酶对这三种肿瘤系统中的任何一种都没有抗肿瘤活性。在两种药物同时联合使用的所有研究中,都观察到β -葡萄糖苷酶增强了苦杏仁苷MF的致死毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental studies of the antitumor activity of amygdalin MF (NSC-15780) alone and in combination with beta-glucosidase (NSC-128056).

Amygdalin MF was evaluated alone and in combination with an activating agent, beta-glucosidase, against three transplantable rodent tumors; Ridgway osteogenic sarcoma, Lewis lung carcinoma, and P388 leukemia. In dose-response studies up to the LD20 in normal mice, amygdalin MF alone did not demonstrate significant antitumor activity against any of these three tumor systems. Similarly, at doses not exceeding the LD10 in normal mice, amygdalin MF plus beta-glucosidase did not demonstrate antitumour activity against any of these three tumor systems. Potentiation of the lethal toxicity of amygdalin MF by beta-glucosidase was observed in all studies where the two agents were given in simultaneous combination.

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