Song Jie-Young, Yang Hyun-Ok, Shim Ji-Young, Han Young-Soo, Jung In-Sung, Yun Yeon-Sook
Laboratory of Immunology, Korea Institute of Radiological and Medical Sciences, KAERI, Seoul, Korea.
Int J Hematol. 2003 Oct;78(3):226-32. doi: 10.1007/BF02983799.
We earlier reported that CM-AIa isolated from Chelidonium majus had mitogenic activity, generated lymphokine-activated killer cells, and increased the number of granulocyte-macrophage colony-forming cells (GM-CFC). In an extended effort to search for other immunostimulatory effects, we evaluated the protective effects of in vivo injected CM-AIa against irradiation. CM-AIa was found to increase the number of bone marrow cells, spleen cells, GM-CFC, and platelets in irradiated mice. In addition, this agent induced endogenous production of cytokines such as interleukin 1 and tumor necrosis factor alpha, which are required for hematopoietic recovery. We also demonstrated that CM-AIa treatment 24 hours before irradiation protected mice with 80% survival at lethal dose 100/15. These findings indicate that CM-AIa may be a useful agent for reducing the time needed for reconstitution of hematopoietic cells after irradiation treatment.
我们之前报道过,从白屈菜中分离出的CM-AIa具有促有丝分裂活性,能产生淋巴因子激活的杀伤细胞,并增加粒细胞-巨噬细胞集落形成细胞(GM-CFC)的数量。为进一步寻找其他免疫刺激作用,我们评估了体内注射CM-AIa对辐射的保护作用。结果发现,CM-AIa可增加受辐射小鼠的骨髓细胞、脾细胞、GM-CFC和血小板数量。此外,该制剂可诱导内源性细胞因子如白细胞介素1和肿瘤坏死因子α的产生,而这些细胞因子是造血恢复所必需的。我们还证明,在辐射前24小时用CM-AIa治疗可使小鼠在致死剂量100/15下的存活率达到80%。这些发现表明,CM-AIa可能是一种有用的药物,可缩短辐射治疗后造血细胞重建所需的时间。