Mian M, Benetti D, Aloisi R, Rosini S, Fantozzi R
Gentili Institute Research Division, Pisa, Italy.
Pharmacology. 1994 Nov;49(5):336-42. doi: 10.1159/000139251.
The effects of three bisphosphonates (BPs), designated 4-amino-1-hydroxybutylidene-1, 1-bisphosphonate (AHBuBP), 6-amino-1-hydroxylidene-1, 1-bisphosphonate (AHHexBP) and chloromethylenebisphosphonate (Cl2MBP), were evaluated on the basis of their effect on the phagocytic activity, lysosomal enzyme release and superoxide anion production in the rat peritoneal macrophage (M phi). AHBuBP was found to inhibit in a concentration-dependent manner the phagocytosis of sheep red blood cells (SRBC). The same activity was seen with the phagocytosis of latex beads, although this effect was independent of calcium concentration. Conversely, AHHexBP and Cl2MBP were weak inhibitors of phagocytosis of both SRBC and latex beads. Inhibition studies on the phorbol myristate acetate-stimulated production of superoxide anion have shown all three BPs to be active. When compared with Cl2MBP, AHBuBP and AHHexBP were shown to be substantially active in inhibiting the release of beta-glucuronidase from ionophore A23187-stimulated rat peritoneal M phi.
基于三种双膦酸盐(BPs),即4-氨基-1-羟基丁叉-1,1-双膦酸盐(AHBuBP)、6-氨基-1-羟基己叉-1,1-双膦酸盐(AHHexBP)和氯亚甲基双膦酸盐(Cl2MBP)对大鼠腹腔巨噬细胞(M phi)吞噬活性、溶酶体酶释放及超氧阴离子产生的影响进行了评估。发现AHBuBP以浓度依赖方式抑制绵羊红细胞(SRBC)的吞噬作用。对乳胶珠吞噬也观察到同样的活性,尽管这种作用与钙浓度无关。相反,AHHexBP和Cl2MBP对SRBC和乳胶珠吞噬的抑制作用较弱。对佛波酯肉豆蔻酸酯乙酸酯刺激产生超氧阴离子的抑制研究表明,所有三种双膦酸盐均有活性。与Cl2MBP相比,AHBuBP和AHHexBP在抑制离子载体A23187刺激的大鼠腹腔M phi释放β-葡萄糖醛酸酶方面显示出显著活性。