Wang Dong-xiao, Liu Ping, Chen Yi-hong, Chen Ruo-yun, Guo Dai-hong, Ren Hao-yang, Chen Meng-li
Department of Pharmacy and Clinical Pharmacology, General Hospital of Chinese PLA, Beijing 100853, China.
Chin Med J (Engl). 2008 Apr 20;121(8):752-5.
Hematopoietic growth factor (HGF) is indispensable to hematopoiesis in the body. The proliferation and differentiation of hematopoietic cells must rely on the existence and stimulation of HGF. This study investigated the effect of catechin, an active component extracted from Spatholobus suberectus Dunn (SSD), on bioactivity of granulocyte-macrophage colony-stimulating activity (GM-CSA), burst-promoting activity (BPA) and megakaryocyte colony-stimulating activity (MK-CSA) in spleen condition medium (SPCM) of mice to clarify the hematopoietic mechanism of catechin and SSD.
Spleen cells of mice were separated and spleen condition medium (SPCM) was prepared from spleen cell culture. Bone marrow cells of mice were separated and cultured in a culture system including 10% (v/v) SPCM (induced by catechin in vivo or ex vivo) for 6 days. Granulocyte-macrophage colony forming units (CFU-GM), erythrocyte burst-colony-forming units (BFU-E) and megakaryocyte colony-forming units (CFU-Meg) formation were employed to assay the effects of different treatment on the bioactivity of GM-CSA, BPA and MK-CSA in SPCM.
SPCM induced by 100 mg/L catechin ex vivo could promote the growth of CFU-GM, BFU-E and CFU-Meg, which indicated that catechin could stimulate the production of GM-CSA, BPA and MK-CSA in SPCM. SPCM prepared at the fourth day of spleen cell culture showed the best stimulating activity. The bioactivity of GM-CSA, BPA and MK-CSA in the SPCM prepared after intraperitoneally injecting catechin into mice was also increased. The number of CFU-GM, BFU-E and CFU-Meg gradually increased as the dose of catechin increased and the time of administration prolonged. CFU-GM, BFU-E and CFU-Meg of the high-dose catechin group were significantly higher than those of the control group (P < 0.01) and reached the maximum at the seventh day after administration.
This study suggests that catechin extracted from the active acetic ether part of Spatholobus suberectus Dunn can regulate hematopoiesis by inducing bioactivity of GM-CSA, BPA and MK-CSA in SPCM of mice. This may be one of the mechanisms for the hematopoietic-supportive effect of catechin and Spatholobus suberectus Dunn.
造血生长因子(HGF)对机体造血过程不可或缺。造血细胞的增殖与分化必须依赖HGF的存在及刺激。本研究探讨了从鸡血藤(SSD)中提取的活性成分儿茶素对小鼠脾条件培养基(SPCM)中粒细胞 - 巨噬细胞集落刺激活性(GM - CSA)、爆式促进活性(BPA)和巨核细胞集落刺激活性(MK - CSA)生物活性的影响,以阐明儿茶素和鸡血藤的造血机制。
分离小鼠脾细胞并制备脾条件培养基(SPCM)用于脾细胞培养。分离小鼠骨髓细胞,在包含10%(v/v)SPCM(体内或体外经儿茶素诱导)的培养体系中培养6天。采用粒细胞 - 巨噬细胞集落形成单位(CFU - GM)、红细胞爆式集落形成单位(BFU - E)和巨核细胞集落形成单位(CFU - Meg)形成实验来检测不同处理对SPCM中GM - CSA、BPA和MK - CSA生物活性的影响。
100 mg/L儿茶素体外诱导的SPCM能促进CFU - GM、BFU - E和CFU - Meg的生长,这表明儿茶素能刺激SPCM中GM - CSA、BPA和MK - CSA的产生。脾细胞培养第4天制备的SPCM显示出最佳刺激活性。小鼠腹腔注射儿茶素后制备的SPCM中GM - CSA、BPA和MK - CSA的生物活性也有所增加。随着儿茶素剂量增加和给药时间延长,CFU - GM、BFU - E和CFU - Meg数量逐渐增加。高剂量儿茶素组的CFU - GM、BFU - E和CFU - Meg显著高于对照组(P < 0.01),并在给药后第7天达到最大值。
本研究表明,从鸡血藤活性乙酸乙酯部位提取的儿茶素可通过诱导小鼠SPCM中GM - CSA、BPA和MK - CSA的生物活性来调节造血。这可能是儿茶素和鸡血藤造血支持作用的机制之一。