Suppr超能文献

在大鼠脊柱融合模型中,通过间歇性给予人甲状旁腺激素(1-34)增强移植骨愈合。

Enhancement of graft bone healing by intermittent administration of human parathyroid hormone (1-34) in a rat spinal arthrodesis model.

作者信息

Abe Yuichiro, Takahata Masahiko, Ito Manabu, Irie Kazuharu, Abumi Kuniyoshi, Minami Akio

机构信息

Department of Orthopaedic Surgery, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Sapporo, Japan.

出版信息

Bone. 2007 Nov;41(5):775-85. doi: 10.1016/j.bone.2007.06.025. Epub 2007 Jul 13.

Abstract

Bone grafting is commonly used to treat skeletal disorders associated with large bone defect or unstable joint. It can take several months, however, to achieve a solid union and bony fusion sometimes delays or fails especially in osteoporosis patients. Therefore, we used a rat spinal arthrodesis model to examine whether intermittent administration of human PTH(1-34) accelerates bone graft healing. Eighty-two male Sprague-Dawley rats underwent posterolateral spinal arthrodesis surgery using autologous bone grafts. Animals were given daily subcutaneous injections of hPTH(1-34) (40 microg/kg/day PTH group) or 0.9% saline vehicle (control group) from immediately after surgery till death. Five rats each were killed 2, 4, 7, and 14 days after the surgery, and mRNA expression analysis was performed on harvested grafted bone. Seven rats each were killed 14, 28, and 42 days after the surgery, and the lumbar spine, which contained the grafted spinal segment, was subjected to fusion assessment, microstructural analysis using three-dimensional micro-computed tomography, and histologic examination. Serum bone metabolism markers were analyzed. The results indicated that PTH administration decreased the time required for graft bone healing and provided a structurally superior fusion mass in the rat spinal arthrodesis model. PTH administration increased the fusion rate on day 14 (14% in the control group and 57% in the PTH group), accelerated grafted bone resorption, and produced a larger and denser fusion mass compared to control. mRNA expression of both osteoblast- and osteoclast-related genes was upregulated by PTH treatment, and serum bone formation and resorption marker levels were higher in the PTH group than in the control group. Histologically calculated mineral apposition rate, mineralized surface and osteoclast surface were also higher in the PTH group than in the control group. These findings suggest that intermittent administration of PTH(1-34) enhanced bone turn over dominantly on bone formation at the graft site, leading to the acceleration of the spinal fusion. Based on the results of this study, intermittent injection of hPTH(1-34) might be an efficient adjuvant intervention in spinal arthrodesis surgery and all other skeletal reconstruction surgeries requiring bone grafts.

摘要

骨移植常用于治疗与大的骨缺损或不稳定关节相关的骨骼疾病。然而,实现牢固的骨愈合可能需要数月时间,并且骨融合有时会延迟或失败,尤其是在骨质疏松患者中。因此,我们使用大鼠脊柱融合模型来研究间歇性给予人甲状旁腺激素(1-34)是否能加速骨移植愈合。82只雄性Sprague-Dawley大鼠接受了使用自体骨移植的后外侧脊柱融合手术。动物从手术后立即开始直至死亡,每天皮下注射hPTH(1-34)(40微克/千克/天PTH组)或0.9%生理盐水载体(对照组)。术后2、4、7和14天各处死5只大鼠,并对收获的移植骨进行mRNA表达分析。术后14、28和42天各处死7只大鼠,对包含移植脊柱节段的腰椎进行融合评估、使用三维微计算机断层扫描进行微观结构分析以及组织学检查。分析血清骨代谢标志物。结果表明,在大鼠脊柱融合模型中,给予PTH减少了移植骨愈合所需的时间,并提供了结构上更优的融合块。给予PTH提高了第14天的融合率(对照组为14%,PTH组为57%),加速了移植骨吸收,与对照组相比产生了更大且更致密的融合块。PTH治疗上调了成骨细胞和破骨细胞相关基因的mRNA表达,PTH组血清骨形成和吸收标志物水平高于对照组。组织学计算的矿物质沉积率、矿化表面和破骨细胞表面在PTH组也高于对照组。这些发现表明,间歇性给予PTH(1-34)主要在移植部位的骨形成上增强了骨转换,从而导致脊柱融合加速。基于本研究结果,间歇性注射hPTH(1-34)可能是脊柱融合手术以及所有其他需要骨移植的骨骼重建手术中的一种有效辅助干预措施。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验