Pataki A, Müller K, Green J R, Ma Y F, Li Q N, Jee W S
Novartis Pharma Inc., Basle, Switzerland.
Anat Rec. 1997 Dec;249(4):458-68. doi: 10.1002/(SICI)1097-0185(199712)249:4<458::AID-AR5>3.0.CO;2-N.
To study the anti-resorptive effects of zoledronate and pamidronate on growing long bones we have performed a histomorphometric analysis of the three regions of the proximal tibial cancellous bone of bone formed before, during, and after drug treatment. Male rats (190-220 g) were treated subcutaneously for 10 days with zoledronate (0.028-2.8 microg/kg) or pamidronate (3.7-370 microg/kg) and sacrificed 5 days later. To delineate the three regions of cancellous bone, and for dynamic bone histomorphometry, calcein and demeclocycline were injected at various times. Both bisphosphonates caused a dose-dependent suppression of cancellous bone turnover and resorption to produce an increase in cancellous bone, but zoledronate was 100 times more potent than pamidronate. The increase in the bone amount and connectivity was more pronounced in the bone formed during treatment where transient bone resorption and normal bone formation led to a positive bone balance. In the bone formed before treatment, inhibition of bone resorption associated with reduced bone formation produced a net gain in amount of bone. Although both bone regions showed a positive bone balance, more bone accumulated in the bone formed during treatment probably because its trabecular bone surface was three times greater. In the primary spongiosa formed after treatment, a moderate increase in the bone amount and connectivity was observed only at the highest dose of both bisphosphonates. The bone formed before, during, and after treatment with bisphosphonates responds differently due to differences in bone architecture, rates of modeling and remodeling, and period of drug exposure.
为研究唑来膦酸和帕米膦酸对生长中的长骨的抗吸收作用,我们对药物治疗前、治疗期间和治疗后形成的胫骨近端松质骨的三个区域进行了组织形态计量学分析。雄性大鼠(190 - 220克)皮下注射唑来膦酸(0.028 - 2.8微克/千克)或帕米膦酸(3.7 - 370微克/千克),持续10天,5天后处死。为了划分松质骨的三个区域并进行动态骨组织形态计量学分析,在不同时间注射了钙黄绿素和地美环素。两种双膦酸盐均引起松质骨转换和吸收的剂量依赖性抑制,从而导致松质骨增加,但唑来膦酸的效力比帕米膦酸强100倍。在治疗期间形成的骨中,骨量和连通性的增加更为明显,此时短暂的骨吸收和正常的骨形成导致了正性骨平衡。在治疗前形成的骨中,骨吸收的抑制与骨形成减少相关,导致骨量净增加。虽然两个骨区域均显示正性骨平衡,但治疗期间形成的骨中积累的骨更多,可能是因为其小梁骨表面积大三倍。在治疗后形成的初级海绵骨中,仅在两种双膦酸盐的最高剂量下观察到骨量和连通性有适度增加。双膦酸盐治疗前、治疗期间和治疗后形成的骨由于骨结构、建模和重塑速率以及药物暴露时间的差异而有不同反应。