Suppression of footpad reaction in mice by anthralin.

M Tabara, M Watanabe
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Abstract

In the preceding papers, we showed that the treatment of BALB/c mice with 12-O-tetradecanoylphorbol 13-acetate (TPA), a typical tumor promoter, suppressed footpad reaction (FPR) against sheep red blood cells (SRBC) temporarily but that this effect became lasting when TPA was administered to mice which had been treated with 7,12-dimethyl[a]-anthracene (DMBA), a typical tumor initiator, and that the effect of DMBA and TPA was caused by the induction of antigen-nonspecific T suppressor cells. In this work, we studied the effect of anthralin, a tumor promoter which has not the structure of phorbol ester, on FPR of BALB/c mice against SRBC. Painting of anthralin (80 nmol) suppressed FPR continuously (more than 7 days) unlike that of TPA. However, when anthralin was administered for 7 days following the treatment with 400 nmol of DMBA, the suppressive effect could be transferred with Thy-1 and Lyt-2 positive spleen cells whereas the suppressive effect by the painting of anthralin only for 7 days could not be transferred with the spleen cells.

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炭疽素对小鼠脚垫反应的抑制作用。
在前面的论文中,我们表明,治疗BALB / c小鼠12-O-tetradecanoylphorbol 13-acetate (TPA),一个典型的肿瘤促进剂,抑制拦路贼反应(玻璃钢)对绵羊红细胞(抗体)暂时,但这种效应成为持久的TPA时对被处理的老鼠注射7,12-dimethyl[一]蒽(DMBA),一个典型的肿瘤启动程序,DMBA和TPA的效果是由antigen-nonspecific T抑制细胞的诱导。本研究研究了一种非酚酯结构的肿瘤启动子——炭疽素对BALB/c小鼠抗SRBC FPR的影响。与TPA不同,80 nmol的炭疽素对FPR的抑制作用持续7天以上。然而,在400 nmol DMBA处理后,再给炭疽碱7天,抑制作用可以在Thy-1和Lyt-2阳性的脾细胞中转移,而只涂炭疽碱7天的抑制作用不能在脾细胞中转移。
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