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在骨固定术之前间歇性给予人甲状旁腺激素可刺激去卵巢大鼠的松质骨愈合。

Intermittent administration of human parathyroid hormone before osteosynthesis stimulates cancellous bone union in ovariectomized rats.

机构信息

Department of Orthopedic Surgery, Akita University Graduate School of Medicine, Akita City, Japan.

出版信息

Tohoku J Exp Med. 2013 Jan;229(1):19-28. doi: 10.1620/tjem.229.19.

Abstract

It has been reported that intermittent administration of human parathyroid hormone (h-PTH) promotes bone healing after surgery for osteoporotic fractures. If bone healing is promoted by the administration of h-PTH during pre-operative waiting period, we can prevent prolonged bed rest. Therefore, we evaluated the effects of pre-operative h-PTH treatment on cancellous bone union and its mechanism for fracture healing in ovariectomized rats as a model for osteoporosis. Ovariectomized 7-month-old female Sprague-Dawley rats underwent an osteotomy of the proximal tibia as a fracture model, and h-PTH (30 μg/kg body weight) or vehicle was administered as a pre-operative treatment for one week. After the one-week treatment, tibiae were fixed with wire for osteosynthesis, and h-PTH or vehicle was administered for 1 or 3 weeks following wire fixation. In addition to bone histomorphometry, we used alcian blue/hematoxylin stained sections for evaluating cartilage volume and immunostained sections for analyzing the expression of proliferating cell nuclear antigen (PCNA) for cell proliferation and that of Sox9 and Runx2, differentiation markers for cartilage cells and osteoblasts, respectively. Pre-operative treatment with PTH significantly increased bone volume. Pre-operative and pre- to post-operative treatment with PTH for 2 weeks significantly promoted bone union. Pre-operative treatment with PTH significantly increased cartilage volume, and pre- to post-operative treatment with PTH for 2 weeks significantly increased the percentage of cells positive for Runx2 (p < 0.01), but not PCNA or Sox9. Pre-operative administration of h-PTH enhances bone union by promoting cartilage formation and cell differentiation to osteoblasts, but not by promoting cell proliferation.

摘要

已有研究报道,间断给予人甲状旁腺激素(h-PTH)可促进骨质疏松性骨折术后骨愈合。如果 h-PTH 在术前等待期给药可促进骨愈合,我们就可以避免长时间卧床。因此,我们评估了术前 h-PTH 治疗对去卵巢大鼠模型(骨质疏松症模型)松质骨愈合的影响及其对骨折愈合的作用机制。7 月龄雌性 Sprague-Dawley 大鼠行胫骨近端截骨术作为骨折模型,h-PTH(30μg/kg 体重)或赋形剂作为术前治疗给药 1 周。1 周治疗后,用金属丝固定胫骨进行骨内固定,在固定后继续给予 h-PTH 或赋形剂 1 或 3 周。除了骨组织形态计量学外,我们还使用阿尔新蓝/苏木精染色切片评估软骨体积,免疫组化染色分析增殖细胞核抗原(PCNA)、Sox9 和 Runx2 的表达,以分别分析细胞增殖和软骨细胞、成骨细胞分化的标志物。术前给予 PTH 可显著增加骨体积。术前和术前至术后 2 周给予 PTH 治疗可显著促进骨愈合。术前给予 PTH 可显著增加软骨体积,而术前至术后 2 周给予 PTH 治疗可显著增加 Runx2 阳性细胞的百分比(p <0.01),但不增加 PCNA 或 Sox9 的阳性细胞百分比。术前给予 h-PTH 通过促进软骨形成和细胞向成骨细胞分化来增强骨愈合,而不是通过促进细胞增殖。

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