Kondo Y, Imai Y, Hojo H, Endo T, Nozoe S
Pharmaceutical Institute, Tohoku University, Sendai, Japan.
J Pharmacobiodyn. 1990 Jul;13(7):426-31. doi: 10.1248/bpb1978.13.426.
The aporphine alkaloids, dicentrine, glaucine, corydine, and apomorphine were shown to have inhibitory activity against several mouse tumor cell lines, leukemia P388 and L1210, melanoma B16, bladder cancer MBC2, and colon cancer Colon 26 in culture. These aporphine alkaloids also inhibited the mitogen-induced lymphocyte proliferation as well as the growth of IL-2 dependent CTLL2 line in a dose-dependent way. Of the four alkaloids apomorphine proved to be most potent in the inhibitory action. Apomorphine treatment resulted in some prolongation of survival time of the mice inoculated i.p. with P388, although its activity was not enough to meet the standard criterion for antitumor activity.
阿朴啡生物碱、双氢黄连碱、青藤碱、紫堇碱和阿扑吗啡在体外培养实验中对几种小鼠肿瘤细胞系具有抑制活性,包括白血病P388和L1210、黑色素瘤B16、膀胱癌MBC2以及结肠癌Colon 26。这些阿朴啡生物碱还能剂量依赖性地抑制丝裂原诱导的淋巴细胞增殖以及IL-2依赖的CTLL2细胞系的生长。在这四种生物碱中,阿扑吗啡的抑制作用最强。阿扑吗啡治疗可使腹腔注射P388的小鼠存活时间有所延长,但其活性不足以达到抗肿瘤活性的标准。