Hyvönen P M, Kowolik M J
Faculty of Dentistry, University of Kuopio, Finland.
Ann Rheum Dis. 1992 Feb;51(2):203-9. doi: 10.1136/ard.51.2.203.
Transmission electron microscopy and standard chemiluminescence assays were used to investigate the in vivo effect of dichloromethylene bisphosphonate (clodronate) on the phagocytosis of pure hydroxyapatite particles by rat peritoneal macrophages and the production of chemiluminescence by the peritoneal exudate cells. Hydroxyapatite (control) and a hydroxyapatite/clodronate suspension (28 mumol clodronate per gram of hydroxyapatite, experimental) were injected into the peritoneum of rats, the clodronate dose being 10 micrograms/kg. Macrophages were harvested at 12, 24, 48, and 96 hours after injection and the particle phagocytosis was assessed by transmission electron microscopy. Hydroxyapatite alone was completely phagocytosed by 24 hours and hydroxyapatite reacted with clodronate was completely phagocytosed by 48 hours. From 48 hours onwards hydroxyapatite particle dissolution was observed in the phagosomes of cells in the two groups. At 48 hours the chemiluminescence produced by the peritoneal exudate cells was also measured. Clodronate and clodronate/hydroxyapatite enhanced cell activity on subsequent challenge with phorbol myristate acetate or zymosan. Clodronate seemed to exhibit an inhibitory effect on the phagocytic activity and an enhancement of the chemiluminescence production by the cells in this model, indicating that it was modifying the inflammatory cell response.
采用透射电子显微镜和标准化学发光分析法,研究二氯亚甲基二膦酸盐(氯膦酸盐)对大鼠腹腔巨噬细胞吞噬纯羟基磷灰石颗粒及腹腔渗出细胞产生化学发光的体内效应。将羟基磷灰石(对照)和羟基磷灰石/氯膦酸盐混悬液(每克羟基磷灰石含28 μmol氯膦酸盐,实验用)注入大鼠腹腔,氯膦酸盐剂量为10 μg/kg。注射后12、24、48和96小时采集巨噬细胞,通过透射电子显微镜评估颗粒吞噬情况。单独的羟基磷灰石在24小时时被完全吞噬,与氯膦酸盐反应的羟基磷灰石在48小时时被完全吞噬。48小时后,两组细胞的吞噬体中均观察到羟基磷灰石颗粒溶解。在48小时时还检测了腹腔渗出细胞产生的化学发光。在用佛波酯或酵母聚糖再次刺激时,氯膦酸盐和氯膦酸盐/羟基磷灰石增强了细胞活性。在该模型中,氯膦酸盐似乎对吞噬活性有抑制作用,并增强了细胞的化学发光产生,表明它在改变炎症细胞反应。