Larsson A, Larsson S E
Acta Pathol Microbiol Scand A. 1978 May;86(3):211-23. doi: 10.1111/j.1699-0463.1978.tb02035.x.
Ethylene-1-hydroxy-1, 1-diphosphonate (EHDP) was administered intraperitoneally to one-day-old rats. In the first experiment, each animal was given 4 injections of EHDP distributed over two consecutive days and corresponding to a total amount of EHDP of 100 mg/kg bwt/day. The animals were sacrificed 12 hours after the last injection. In the second experiment, each animal was given 3 injections, each containing 50 mg of EHDP/kg bwt, with an interval of 6 hours and were thereafter left to survive for 4 days. Animals in the first experiment showed in comparison to normal controls an increased width of the hypertrophic zone; lack of calcified septa within the zone of provisional calcification; persistent atypical chondrocytes in the calcification zone and a large number of matrix vesicles lacking in crystals. The ground substance showed an accumulation of fine precipitates apparently representing undegraded aggregates of proteoglycan macromolecules. Animals in the second experiment formed a new apparently normal epiphyseal growth plate, while the "old" epiphyseal cartilage formed under the influence of EHDP remained largely unresorbed within the metaphysis. Besides the previously described inhibitory effects of diphosphonates on the crystallization of matrix vesicles and the growth of hydroxyapatite crystals, EHDP, at the doses used, was found to have a profound inhibitory effect on the differentiation and migration of the epiphyseal chondrocytes as well as on the degradation of proteoglycan macromolecules. The observed inhibition of vascular invasion appears to be related to inhibition of enzyme degradation of the ground substance, as evidenced by the observation of extracellular lysosomelike bodies in the erosion zone.
将乙烯 - 1 - 羟基 - 1,1 - 二膦酸盐(EHDP)腹腔注射给1日龄大鼠。在第一个实验中,每只动物连续两天接受4次EHDP注射,相当于EHDP总量为100mg/kg体重/天。在最后一次注射后12小时处死动物。在第二个实验中,每只动物接受3次注射,每次注射含50mg EHDP/kg体重,间隔6小时,之后存活4天。与正常对照组相比,第一个实验中的动物显示肥大带宽度增加;临时钙化区内缺乏钙化隔;钙化区内持续存在非典型软骨细胞,并且大量基质小泡缺乏晶体。基质显示有细沉淀物积聚,显然代表蛋白聚糖大分子的未降解聚集体。第二个实验中的动物形成了一个新的明显正常的骨骺生长板,而在EHDP影响下形成的“旧”骨骺软骨在干骺端内大部分未被吸收。除了双膦酸盐对基质小泡结晶和羟基磷灰石晶体生长的先前描述的抑制作用外,发现所用剂量的EHDP对骨骺软骨细胞的分化和迁移以及蛋白聚糖大分子的降解具有深远的抑制作用。观察到的血管侵入抑制似乎与基质酶降解的抑制有关,在侵蚀区内观察到细胞外溶酶体样小体证明了这一点。