Zhang J P, Qian D H, Zheng Q Y
Research Laboratory of Natural and Synthetic Drugs, College of Pharmacy, Second Military Medical University, Shanghai, China.
Zhongguo Yao Li Xue Bao. 1990 Jul;11(4):375-7.
The in vivo effects of Phytolacca acinosa polysaccharides I (PEP-I) on immunologic cytotoxicity of mouse peritoneal macrophages and its production of tumor necrosis factor (TNF) and interleukin 1 (IL-1) were studied. PEP-I 80, 160 mg/kg was given ip twice every 4 d. Both doses were found to have significant enhancing activity on macrophages cytotoxicity against S180 sarcoma cells and malignant transformed fibroblast L929 cells. Peritoneal activated macrophages were incubated with LPS for 2 and 24 h to induce TNF and IL-1, respectively. The TNF and IL-1 activities were tested from cytotoxicity against L929 cells in an absorbance assay of enzymatic reaction and proliferation of thymocytes co-stimulated assay separately. The optimal time for TNF production was found on d 8. Significant increases in TNF and IL-1 were observed. In comparison of the effect of PEP-I on TNF with that of known priming agent BCG, there was no difference between these two, but PEP-I had a high effect on IL-1. These results suggest that cytotoxicity of macrophages primed by PEP-I is closely related to its TNF and IL-1 production.
研究了商陆多糖I(PEP-I)对小鼠腹腔巨噬细胞免疫细胞毒性及其肿瘤坏死因子(TNF)和白细胞介素1(IL-1)产生的体内作用。以80、160mg/kg的PEP-I每4天腹腔注射给药2次。发现这两种剂量对巨噬细胞针对S180肉瘤细胞和恶性转化成纤维细胞L929细胞的细胞毒性均具有显著增强活性。将腹腔活化巨噬细胞分别与LPS孵育2小时和24小时以诱导TNF和IL-1。分别通过酶反应吸光度测定法中针对L929细胞的细胞毒性以及共刺激的胸腺细胞增殖测定法来检测TNF和IL-1活性。发现第8天是产生TNF的最佳时间。观察到TNF和IL-1显著增加。将PEP-I对TNF的作用与已知的启动剂卡介苗的作用进行比较,两者之间没有差异,但PEP-I对IL-1有高效应。这些结果表明,由PEP-I启动的巨噬细胞的细胞毒性与其TNF和IL-1的产生密切相关。