彭宗根, 陈鸿珊, 郭志敏, 董飚, 田庚元, 王光强. 牛膝多糖硫酸酯体外和体内抗艾滋病病毒作用J. 药学学报, 2008, 43(7): 702-706.
引用本文: 彭宗根, 陈鸿珊, 郭志敏, 董飚, 田庚元, 王光强. 牛膝多糖硫酸酯体外和体内抗艾滋病病毒作用J. 药学学报, 2008, 43(7): 702-706.
PENG Zong-gen, CHEN Hong-shan, GUO Zhi-min, DONG Biao, TIAN Geng-yuan, WANG Guang-qiang. Anti-HIV activities of Achyranthes bidentata polysaccharide sulfate in vitro and in vivoJ. Acta Pharmaceutica Sinica, 2008, 43(7): 702-706.
Citation: PENG Zong-gen, CHEN Hong-shan, GUO Zhi-min, DONG Biao, TIAN Geng-yuan, WANG Guang-qiang. Anti-HIV activities of Achyranthes bidentata polysaccharide sulfate in vitro and in vivoJ. Acta Pharmaceutica Sinica, 2008, 43(7): 702-706.

牛膝多糖硫酸酯体外和体内抗艾滋病病毒作用

Anti-HIV activities of Achyranthes bidentata polysaccharide sulfate in vitro and in vivo

  • 摘要: 牛膝多糖硫酸酯(Achyranthes bidentata polysaccharide sulfate,ABPS)为牛膝多糖经硫酸酯化修饰后获得的产物,其结构清楚、理化性质稳定及分子质量小,具有抗单纯疱疹病毒、柯萨奇病毒和乙型肝炎病毒等作用。本文研究其在体外和体内的抗艾滋病病毒1型(human immunodeficiency virus type 1,HIV-1)活性。体外采用 3H掺入法和酶联免疫吸附法测定ABPS对HIV-1逆转录酶和整合酶的活性,其半数抑制浓度(50% inhibiting concentrations,IC50)分别为(2.948±0.556) μmol·L-1和(0.155±0.030) μmol·L-1, 但25 μmol·L-1 ABPS对HIV-1蛋白酶无效。ABPS在MT-4细胞培养内对HIV-1实验病毒株IIIB和在人外周血单核细胞培养内对AZT耐药病毒株的急性感染有较强的抑制作用, 但在HIV-1 IIIB慢性感染的H9细胞培养中则无效。血清药理学研究表明,单次腹腔注射大鼠ABPS 125 mg·kg-1或连续腹腔注射小鼠ABPS 3 mg·kg-1(qd×20)后鼠血清在MT-4细胞培养内对HIV-1 P24抗原都有抑制作用,但口服ABPS生物利用度低,灌胃大鼠ABPS 2 g·kg-1或灌胃小鼠ABPS 300 mg·kg-1无效。实验结果提示ABPS有抗HIV-1作用,有可能用于防治HIV-1感染,值得进一步研究。

     

    Abstract: Achyranthes bidentata polysaccharide sulfate (ABPS) was a sulfated derivate derived from Achyranthes bidentata polysaccharide (ABP) which was isolated and identified from Chinese herb Achyranthes bidentata. The anti human immunodeficiency virus type 1 (HIV-1) activities were studied in vitro and in vivo. ABPS was found to inhibit HIV-1 reverse transcriptase and integrase with the 50% inhibiting concentration (IC50) of (2.948±0.556) μmol·L-1 and (0.155±0.030) μmol·L-1, respectively, but the parent compound ABP was not effective. ABPS inhibited HIV-1 P24 antigen with IC50 of (0.082±0.044) μmol·L-1 and selective index (SI) of >(358±148) in MT-4 cell cultures acutely infected with HIV-1 IIIB virus, and with IC50 of (11.80±5.90) μmol·L-1 and SI of >(24.2±12.1) in PBMC cell cultures acutely infected with clinical isolated zidovudine resistant HIV-1 virus, but there was no activity even at its concentration of 500 μmol·L-1 in latent infection of H9/ HIV-1 IIIB cell cultures. 5% sera taken from rats after intraperitoneal injection from rats with ABPS 125 mg·kg-1 once or mice with 3 mg·kg-1 qd for 20 days effectively inhibited HIV-1 P24 in MT-4 cell cultures, but those had no inhibitory effect when given orally. The results suggested that ABPS is a promising HIV-1 inhibitor, active on HIV-1 reverse transcriptase, integrase in vitro and HIV-1 P24 antigens in cell cultures, it was well absorbed by intraperitoneal injection but poor in oral bioavailability. It warrants further study.

     

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