Wang H B, Zheng Q Y, Qian D H, Fang J, Ju D W
Department of Pharmacology, College of Pharmacy, Second Military Medical University, Shanghai, China.
Zhongguo Yao Li Xue Bao. 1993 May;14(3):243-6.
Radioactivities of [3H]TdR uptaken by splenocytes and released from [3H]TdR-labeled YAC-1 cell line were measured to determine the degree of lymphocyte proliferation and natural killer (NK) cell activity. Seven days after mice treated with Phytolacca acinosa polysaccharides I (PAP-I) 5-50 mg.kg-1, the NK cell activity, and lymphocyte proliferation induced by Con A 5 micrograms.ml-1 or lipopolysaccharides 10 micrograms.ml-1 were significantly augmented. Splenocytes from mice treated with ip PAP-I 5-50 mg.kg-1 were incubated with Con A 5 micrograms.ml-1 for 24 h to induce interleukin-2 (IL-2) and for 40 h to induce NK cytotoxic factor (NKCF). Radioactivities of [3H]TdR uptaken by CTLL-2 cell line and YAC-1 cell line were used to measure the IL-2 and NKCF activities, respectively. PAP-I enhanced the production of IL-2 and NKCF. These results suggest that PAP-I augments the immunological functions in vivo.
通过测量脾细胞摄取的[³H]TdR放射性以及从[³H]TdR标记的YAC - 1细胞系释放的放射性,来确定淋巴细胞增殖程度和自然杀伤(NK)细胞活性。用商陆多糖I(PAP - I)5 - 50mg·kg⁻¹处理小鼠7天后,NK细胞活性以及由5μg·ml⁻¹刀豆蛋白A(Con A)或10μg·ml⁻¹脂多糖诱导的淋巴细胞增殖显著增强。用腹腔注射PAP - I 5 - 50mg·kg⁻¹处理的小鼠脾细胞与5μg·ml⁻¹Con A孵育24小时以诱导白细胞介素 - 2(IL - 2),孵育40小时以诱导NK细胞毒性因子(NKCF)。分别用CTLL - 2细胞系和YAC - 1细胞系摄取的[³H]TdR放射性来测量IL - 2和NKCF活性。PAP - I增强了IL - 2和NKCF的产生。这些结果表明PAP - I在体内增强了免疫功能。