Radiobiology Division, University of Utah School of Medicine, Salt Lake City, UT 84108-1218, USA.
Bone. 2010 Sep;47(3):529-33. doi: 10.1016/j.bone.2010.05.032. Epub 2010 Jun 1.
The current report describes the skeletal effects of a sclerostin monoclonal antibody (Scl-AbIII) treatment at a yellow (fatty) marrow skeletal site in adult female rats. Ten-month-old female Sprague-Dawley rats were treated with vehicle or Scl-AbIII at 5 or 25 mg/kg, twice per week by s.c. injection for 4 weeks. Trabecular bone from a yellow (fatty) marrow site, the 5th caudal vertebral body (CVB), was processed undecalcified for quantitative bone histomorphometric analysis. Compared to vehicle controls, Scl-AbIII at both doses significantly increased bone formation parameters and trabecular bone volume and thickness and decreased bone resorption parameter in the trabecular bone of the CVB. As a reference, we also found that the Scl-AbIII at both doses significantly decreased bone resorption and increased bone formation and bone volume in a red (hematopoietic) marrow site, the 4th lumber vertebral body (LVB). It appears that the percentage of increase in trabecular bone volume induced by Scl-AbIII treatment was slightly larger in the LVB than in the CVB. In summary, these preclinical findings show that antibody-mediated sclerostin inhibition has significant bone anabolic effects at both red and yellow marrow skeletal sites.
本报告描述了在成年雌性大鼠黄色(脂肪)骨髓骨骼部位使用硬化素单克隆抗体(Scl-AbIII)治疗的骨骼效应。10 月龄雌性 Sprague-Dawley 大鼠通过皮下注射,每周两次,分别以 5 或 25mg/kg 的剂量接受载体或 Scl-AbIII 治疗 4 周。对来自黄色(脂肪)骨髓部位的小梁骨(第 5 尾骨椎体 [CVB])进行不脱钙处理,以进行定量骨组织形态计量学分析。与载体对照组相比,两种剂量的 Scl-AbIII 均显著增加了 CVB 小梁骨的骨形成参数、小梁骨体积和厚度,并降低了骨吸收参数。作为参考,我们还发现两种剂量的 Scl-AbIII 均显著降低了红(造血)骨髓部位(第 4 腰椎体 [LVB])的骨吸收,增加了骨形成和骨体积。似乎 Scl-AbIII 治疗引起的小梁骨体积增加百分比在 LVB 比在 CVB 中略大。总之,这些临床前发现表明,硬化素抗体抑制在红骨髓和黄骨髓骨骼部位均具有显著的骨合成作用。