Kawakami Y, Klein T W, Newton C, Djeu J Y, Specter S, Friedman H
Department of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa 33612.
Int J Immunopharmacol. 1988;10(4):485-8. doi: 10.1016/0192-0561(88)90137-3.
The major psychoactive marijuana component, delta-9-tetrahydrocannabinol (THC), suppressed proliferation of murine spleen cells stimulated with recombinant human interleukin 2 (IL-2) and also suppressed the appearance of the lymphokine-activated killer (LAK) cell phenomenon in IL-2-treated spleen cell preparations. Cell function was depressed in a dose-dependent manner with as little as 2.5 micrograms/ml THC (8 microM). In addition, spleen cells previously stimulated in culture with IL-2 and then incubated with THC for 4 h prior to target cell addition, displayed suppressed cytolytic activity against both YAC-1 and EL-4 tumor targets. Killing of EL 4 cells was suppressed at lower drug doses than the killing of YAC-1 targets. These results suggest that THC can suppress several important functions of IL-2 including clonal expansion of lymphocytes, expansion of killer cell populations and stimulation of killer cell cytotoxic activity.
大麻的主要精神活性成分Δ⁹-四氢大麻酚(THC)抑制了重组人白细胞介素2(IL-2)刺激的小鼠脾细胞的增殖,还抑制了IL-2处理的脾细胞制剂中淋巴因子激活的杀伤(LAK)细胞现象的出现。细胞功能以剂量依赖的方式受到抑制,低至2.5微克/毫升的THC(8微摩尔)即可产生这种作用。此外,先前在培养中用IL-2刺激、然后在加入靶细胞前与THC孵育4小时的脾细胞,对YAC-1和EL-4肿瘤靶标的细胞溶解活性均受到抑制。与杀死YAC-1靶标相比,较低剂量的药物就能抑制对EL-4细胞的杀伤。这些结果表明,THC可以抑制IL-2的几种重要功能,包括淋巴细胞的克隆扩增、杀伤细胞群体的扩增以及杀伤细胞细胞毒性活性的刺激。