王洪斌, 陈维中, 包尔基, 郑钦岳, 宋梁, 方军, 徐一新, 陈海生. 商陆多糖Ⅰ联合白细胞介素2对小鼠脾细胞杀瘤活性的影响J. 药学学报, 1995, 30(6): 401-407.
引用本文: 王洪斌, 陈维中, 包尔基, 郑钦岳, 宋梁, 方军, 徐一新, 陈海生. 商陆多糖Ⅰ联合白细胞介素2对小鼠脾细胞杀瘤活性的影响J. 药学学报, 1995, 30(6): 401-407.
HB Mang, WZ Chen, EJ Bao, QY Zheng, HL Song, J Fang, YX Xu , HS Chen, . EFFECTS OF PHYTOLACCA ACINOSA POLYSACCHARIDESI COMBLNED WITH INTERLEUKIN-O ON THE CYTOTOXICITY OF MURINE SPLENOCYTES AGAINST TUMOR CELLSJ. Acta Pharmaceutica Sinica, 1995, 30(6): 401-407.
Citation: HB Mang, WZ Chen, EJ Bao, QY Zheng, HL Song, J Fang, YX Xu , HS Chen, . EFFECTS OF PHYTOLACCA ACINOSA POLYSACCHARIDESI COMBLNED WITH INTERLEUKIN-O ON THE CYTOTOXICITY OF MURINE SPLENOCYTES AGAINST TUMOR CELLSJ. Acta Pharmaceutica Sinica, 1995, 30(6): 401-407.

商陆多糖Ⅰ联合白细胞介素2对小鼠脾细胞杀瘤活性的影响

EFFECTS OF PHYTOLACCA ACINOSA POLYSACCHARIDESI COMBLNED WITH INTERLEUKIN-O ON THE CYTOTOXICITY OF MURINE SPLENOCYTES AGAINST TUMOR CELLS

  • 摘要: 商陆多糖Ⅰ(PAP-I),0.3~3μg·ml-1和小鼠脾细胞培养3~5d可显著增强其杀伤P815肿瘤细胞活性及IL-2(250~500IU·ml-1)诱导的LAK细胞活性,最适浓度为1μg·ml-1。PAP-I及IL-2和脾细胞培养的上清液对P815肿瘤细胞无细胞毒作用,但能增强脾细胞及LAK细胞杀瘤活性。PAP-I,5,10及50mg·kg-1,ip可增强脾细胞杀伤P815和L929细胞的活性及IL-2诱导的LAK细胞活性。

     

    Abstract: Phytolacca acinosaccharides I(PAP-I),a kind of purified polysac- charides,isolated from Phytolacca acinosa Roxb was found to significantly augment the cyto- toxicity of murine splenocytes and interleukin-2( IL-2)activated splenocytes against P815 tumor cells in uitro. The optimal concentration of PAP-I was 1μg·ml-1 and the peak level of the cytotoxicity against P815 tumor cells was reached on d 3~5.The supernatants collected from splenocytes cultured with PAP-I alone or in combination with IL-2 showed no effect on the cytotoxicity against P815 tumor cells.Splenocytes from mice injected ip with PAP-I,5, 10 and 50 mg·kg-1 ,thrice a week produced more cytotoxicity against P815 and L929 tumor cells compared with the control group.PAP-I ip was shown to significantly increase IL-2 activated killer cell activity(LAK)against P815 tumor cells.The higher the dosage of PAP-I,the more potent the LAK activity was observed.These results confirmed that PAP-I can augment the cytotoxicity of murine splenocyte against tumor cells and LAK activity and warranted further evaluation of its clinical usefulness.

     

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